Late Effects of Treatment for Childhood Cancer (PDQ®): Treatment - Patient Information [NCI]

General Information about Late Effects

Late effects are health problems that occur months or years after cancer treatment has ended.

Cancer treatments may harm the body's organs, tissues, or bones and cause health problems later in life. These health problems are called late effects.

Treatments that may cause late effects include the following:

• Surgery.
• Chemotherapy.
• Radiation therapy.
• Stem cell transplant.

Doctors are studying the late effects caused by cancer treatment. They are working to improve cancer treatments and stop or lessen late effects. While most late effects are not life-threatening, they may cause serious problems that affect health and quality of life.

Late effects in childhood cancer survivors affect the body and mind.

Late effects in childhood cancer survivors may affect the following:

• Organs, tissues, and body function.
• Growth and development.
• Mood, feelings, and actions.
• Thinking, learning, and memory.
• Social and psychological adjustment.
• Risk of second cancers.

There are three important factors that affect the risk of late effects.

Many childhood cancer survivors will have late effects. The risk of late effects depends on factors related to the tumor, treatment, and patient. These include the following:

• Tumor-related factors
  • Type of cancer.
  • Where the tumor is in the body.
  • How the tumor affects the way tissues and organs work.
• Treatment-related factors
  • Type of surgery.
  • Chemotherapy type, dose, and schedule.
  • Type of radiation therapy, part of the body treated, and dose.
  • Stem cell transplant.
  • Use of two or more types of treatment at the same time.
  • Chronic graft-versus-host disease.
• Patient-related factors
  • The child's sex.
  • Health problems the child had before being diagnosed with cancer.
  • The child's age and developmental stage when diagnosed and treated.
  • Length of time since diagnosis and treatment.
  • Changes in hormone levels.
  • The ability of healthy tissue affected by cancer treatment to repair itself.
  • Certain changes in the child's genes.
  • Family history of cancer or other conditions.
  • Socioeconomic status.
  • Health habits.

The chance of having late effects increases over time.

New treatments for childhood cancer have decreased the number of deaths from the primary cancer. Because childhood cancer survivors are living longer, they are having more late effects after cancer treatment. Survivors may not live as long as people who did not have cancer. The most common causes of death in childhood cancer survivors are:

• The primary cancer comes back.
• A second (different) primary cancer forms.
• Heart and lung damage.

Studies of the causes of late effects have led to changes in treatment. This has improved the quality of life for cancer survivors and helps prevent illness and death from late effects.

Regular follow-up care is very important for survivors of childhood cancer.

Regular follow-up by health professionals who are trained to find and treat late effects is important for the long-term health of childhood cancer survivors. Follow-up care will be different for each person who has been treated for cancer. The type of care will depend on the type of cancer, the type of treatment, genetic factors, other medical conditions, and the person's general health and health habits. Follow-up care includes checking for signs and symptoms of late effects and health education on how to prevent or lessen late effects.

It is important that childhood cancer survivors have an exam at least once a year. The exams should be done by a health professional who knows the survivor's risk for late effects and can recognize the early signs of late effects. Blood and imaging tests may also be done.

Long-term follow-up may improve the health and quality of life for cancer survivors. It also helps doctors study the late effects of cancer treatments so that safer therapies for newly diagnosed children may be developed.

Good health habits are also important for survivors of childhood cancer.

The quality of life for cancer survivors may be improved by behaviors that promote health and well-being. These include a healthy diet, exercise, and regular medical and dental checkups. These self-care behaviors are especially important for cancer survivors because of their risk of health problems related to treatment. Healthy behaviors may make late effects less severe and lower the risk of other diseases.

Avoiding behaviors that are damaging to health is also important. Smoking, excess alcohol use, illegal drug use, being exposed to sunlight, or not being physically active may worsen organ damage related to treatment and may increase the risk of second cancers.

Second Cancers

Childhood cancer survivors have an increased risk of a second cancer later in life.

A different primary cancer that occurs at least two months after cancer treatment ends is called a second cancer. A second cancer may occur months or years after treatment is completed. The type of second cancer that occurs depends in part on the original type of cancer and the cancer treatment. Benign tumors (not cancer) may also occur.

Second cancers that occur after cancer treatment include the following:

• Myelodysplastic syndrome and acute myeloid leukemia.
• Solid tumors.

Myelodysplastic syndrome and acute myeloid leukemia may appear less than 10 years after a primary cancer diagnosis of Hodgkin lymphoma, acute lymphoblastic leukemia, sarcoma, central nervous system (CNS) tumor, non-Hodgkin lymphoma, neuroblastoma, or Wilms tumor and treatment with chemotherapy that included the following:

• An alkylating agent, such as cyclophosphamide, ifosfamide, mechlorethamine, melphalan, busulfan, carmustine, lomustine, chlorambucil, or dacarbazine.
• A topoisomerase II inhibitor agent, such as etoposide.

Patients treated with radiation to the bone marrow without chemotherapy may also have an increased risk of second acute myeloid leukemia.

Solid tumors that may appear more than 10 years after a primary cancer diagnosis and treatment include the following:

• Breast cancer. There is an increased risk of breast cancer after treatment with high-dose chest radiation treatment for Hodgkin lymphoma at age 30 or younger. Patients treated with radiation above the diaphragm that does not include lymph nodes in the armpit have a lower risk of breast cancer.

  The treatment of cancer that has spread to the chest or lung with chest radiation in the area of the breast may also increase the risk of breast cancer.

  There is also an increased risk of breast cancer in patients who were treated with alkylating agents and anthracyclines but not with chest radiation. The risk is highest in sarcoma and leukemia survivors.

• Thyroid cancer. Thyroid cancer may occur after neck radiation treatment for Hodgkin lymphoma, acute lymphocytic leukemia, or brain tumors; after radioactive iodine therapy for neuroblastoma; after total-body irradiation as part of a stem cell transplant; or after chemotherapy alone.
• Brain tumors. Brain tumors may occur after radiation treatment to the head and/or intrathecal chemotherapy using methotrexate for a primary brain tumor or for cancer that has spread to the brain or spinal cord, such as acute lymphocytic leukemia or non-Hodgkin lymphoma. When intrathecal chemotherapy using methotrexate and radiation treatment are given together, the risk of a brain tumor is even higher. Neurological signs may include seizures, problems with hearing, vision, or balance, and severe headaches.
• Bone and soft tissue tumors. There is an increased risk of bone and soft tissue tumors after radiation treatment for hereditary retinoblastoma, Ewing sarcoma, and other cancers of the bone, with risks increasing at higher doses.

  Chemotherapy with anthracyclines or alkylating agents also increases the risk of bone and soft tissue tumors, with risk increasing at higher doses.

• Lung cancer. There is an increased risk of lung cancer after radiation treatment to the chest for Hodgkin lymphoma, especially in patients who smoke.
• Stomach, liver, or colorectal cancer. Stomach, liver, or colorectal cancer may occur after radiation treatment to the abdomen or pelvis. The risk increases with higher doses of radiation. There is also an increased risk of colorectal polyps. Screening of patients at risk of early-onset colorectal cancer includes a colonoscopy every 5 years or a multitarget stool DNA test every 3 years, beginning at age 30 or 5 years after radiation therapy (whichever occurs later).

  Treatment with chemotherapy alone or chemotherapy and radiation treatment combined also increases the risk of stomach, liver, or colorectal cancer.

• Nonmelanoma skin cancer (basal cell carcinoma or squamous cell carcinoma). There is an increased risk of nonmelanoma skin cancer after radiation treatment, and it usually appears in the area where radiation was given. Being exposed to UV radiation may increase this risk. Patients who develop nonmelanoma skin cancer after radiation treatment have an increased chance of developing other types of cancers in the future. The risk of basal cell carcinoma is also increased after treatment with chemotherapy drugs, called vinca alkaloids, such as vincristine and vinblastine. Survivors of hereditary retinoblastoma may have an increased risk of developing nonmelanoma skin cancer.
• Malignant melanoma. Malignant melanoma may occur after radiation or combination chemotherapy with alkylating agents and antimitotic drugs (such as vincristine and vinblastine). Survivors of Hodgkin lymphoma, hereditary retinoblastoma, soft tissue sarcoma, and gonadal tumors are more likely to be at a higher risk of having malignant melanoma. Malignant melanoma as a second cancer is less common than nonmelanoma skin cancer.
• Oral cavity cancer. Oral cavity cancer may occur after stem cell transplant and a history of chronic graft-versus-host disease.
• Kidney cancer. There is an increased risk of kidney cancer after treatment for neuroblastoma, radiation treatment to the middle of the back, or chemotherapy such as cisplatin or carboplatin.
• Bladder cancer. Bladder cancer may occur after chemotherapy with cyclophosphamide. Survivors of heritable retinoblastoma have an increased risk of developing bladder cancer.

Certain genetic patterns or syndromes may increase the risk of a second cancer.

Some childhood cancer survivors may have an increased risk of developing a second cancer because they have a family history of cancer, an inherited cancer syndrome such as Li-Fraumeni syndrome, or a genetic mutation such as neurofibromatosis type 1. Problems with the way DNA is repaired in cells and the way anticancer drugs are used by the body may also affect the risk of second cancers.

Patients who have been treated for cancer need regular screening tests to check for a second cancer.

It is important for patients who have been treated for cancer to be checked for a second cancer before symptoms appear. This is called screening and may help find a second cancer at an early stage. When abnormal tissue or cancer is found early, it may be easier to treat. By the time symptoms appear, cancer may have begun to spread.

It is important to remember that your child's doctor does not necessarily think your child has cancer if he or she suggests a screening test. Screening tests are given when your child has no cancer symptoms. If a screening test result is abnormal, your child may need to have more tests done to find out if he or she has a second cancer. These are called diagnostic tests.

The kind of test used to screen for a second cancer depends in part on the kind of cancer treatment the patient had in the past.

All patients who have been treated for cancer should have a physical exam and medical history done once a year. A physical exam of the body is done to check general signs of health, including checking for signs of disease, such as lumps, changes in the skin, or anything else that seems unusual. A medical history is taken to learn about the patient's health habits and past illnesses and treatments.

If the patient received radiation therapy, the following tests and procedures may be used to check for skin, breast, or colorectal cancer:

• Skin exam: A doctor or nurse checks the skin for bumps or spots that look abnormal in color, size, shape, or texture, especially in the area where radiation was given. It is suggested that a skin exam be done once a year to check for signs of skin cancer.
• Breast self-exam: An exam of the breast by the patient. The patient carefully feels the breasts and under the arms for lumps or anything else that seems unusual. It is suggested that women treated with a higher dose of radiation therapy to the chest do a monthly breast self-exam beginning at puberty. Women who were treated with a lower dose of radiation to the chest may not need to begin checking for breast cancer at puberty. Talk to your doctor about when you should begin breast self-exams.
• Clinical breast exam (CBE): An exam of the breast by a doctor or other health professional. The doctor will carefully feel the breasts and under the arms for lumps or anything else that seems unusual. It is suggested that women treated with a higher dose of radiation therapy to the chest have a clinical breast exam every year beginning at puberty until age 25. After age 25 or 8 years after radiation treatments end (whichever is first), clinical breast exams are done every 6 months. Women who were treated with a lower dose of radiation to the chest may not need to begin checking for breast cancer at puberty. Talk to your doctor about when you should begin clinical breast exams.
• Mammogram: An x-ray of the breast. A mammogram may be done in women who had a higher dose of radiation to the chest and who do not have dense breasts. It is suggested that these women have a mammogram once a year starting 8 years after treatment or at age 25, whichever is later. Talk to your doctor about when you should begin to have mammograms to check for breast cancer.
• Breast MRI (magnetic resonance imaging): A procedure that uses a magnet, radio waves, and a computer to make a series of detailed pictures of the breast. This procedure is also called nuclear magnetic resonance imaging (NMRI). An MRI may be done in women who had a higher dose of radiation to the chest and who have dense breasts. It is suggested that these women have an MRI once a year starting 8 years after treatment or at age 25, whichever is later. If you had radiation to the chest, talk to your doctor about whether you need an MRI of the breast to check for breast cancer.
• Colonoscopy: A procedure to look inside the rectum and colon for polyps, abnormal areas, or cancer. A colonoscope is inserted through the rectum into the colon. A colonoscope is a thin, tube-like instrument with a light and a lens for viewing. It may also have a tool to remove polyps or tissue samples, which are checked under a microscope for signs of cancer. It is suggested that childhood cancer survivors who had a higher dose of radiation to the abdomen, pelvis, or spine have a colonoscopy every 5 years. This begins at age 30 or 5 years after treatment ended, whichever is later. If you had radiation to the abdomen, pelvis, or spine, talk to your doctor about when you should begin to have colonoscopies to check for colorectal cancer.
• Multitarget stool DNA test: A test to collect stool to check for cancer cells. This test may be done every 3 years beginning at age 30 or 5 years after treatment ended.

Cardiovascular System

Heart and blood vessel late effects are more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause heart and blood vessel late effects:

• Acute lymphoblastic leukemia (ALL).
• Acute myelogenous leukemia (AML).
• Brain and spinal cord tumors.
• Head and neck cancer.
• Hodgkin lymphoma.
• Non-Hodgkin lymphoma.
• Osteosarcoma.
• Wilms tumor.
• Cancers treated with a stem cell transplant.

Radiation to the chest and certain types of chemotherapy increase the risk of heart and blood vessel late effects.

The risk of health problems involving the heart and blood vessels increases after treatment with the following:

• Radiation to the chest, spine, brain, neck, kidneys, or total-body irradiation (TBI) as part of a stem cell transplant. The risk of problems depends on the area of the body that was exposed to radiation, the amount of radiation given, and whether the radiation was given in small or large doses.
• Certain types of chemotherapy and the total dose of anthracycline given. Chemotherapy with anthracyclines such as doxorubicin, daunorubicin, idarubicin, and epirubicin, and with anthraquinones such as mitoxantrone increase the risk of heart and blood vessel problems. The risk of problems depends on the total dose of chemotherapy given and the type of drug used. It also depends on whether treatment with anthracyclines was given to a child younger than 13 years and whether a drug called dexrazoxane was given during treatment with anthracyclines. Dexrazoxane may lessen heart and blood vessel damage up to 5 years after treatment. Ifosfamide, cyclophosphamide, methotrexate, asparaginase, and chemotherapy with platinum, such as carboplatin and cisplatin, may also cause heart and blood vessel late effects.
• Stem cell transplant.
• Nephrectomy (surgery to remove all or part of a kidney).

Childhood cancer survivors who were treated with radiation therapy to the heart or blood vessels and certain types of chemotherapy are at greatest risk.

New treatments that decrease the amount of radiation given and use lower doses of chemotherapy or less harmful chemotherapy drugs may lessen the risk of heart and blood vessel late effects compared with older treatments.

The following may also increase the risk of heart and blood vessel late effects:

• Longer time since treatment.
• Having high blood pressure or other risk factors for heart disease, such as a family history of heart disease, being overweight, smoking, high cholesterol, or diabetes. When these risk factors are combined, the risk of late effects is even higher.
• Having lower than normal amounts of thyroid, growth, or sex hormones.

Late effects that affect the heart and blood vessels may cause certain health problems.

Childhood cancer survivors who received radiation or certain types of chemotherapy have an increased risk of late effects to the heart and blood vessels and related health problems. These include the following:

• Abnormal heartbeat.
• Weakened heart muscle.
• Inflamed heart or sac around the heart.
• Damage to the heart valves.
• Coronary artery disease (hardening of the heart arteries).
• Congestive heart failure.
• Chest pain or heart attack.
• Blood clots or one or more strokes.
• Carotid artery disease.

Childhood cancer survivors may have late effects that affect the heart during pregnancy.

Long-term survivors of childhood, adolescent, and young adult cancers who have received radiation therapy or certain types of chemotherapy are at risk of a rare type of heart failure during pregnancy called peripartum cardiomyopathy (PPCM). It may occur during late pregnancy and up to 5 months after giving birth. Patients at risk of this condition should be closely followed for weakness of the heart muscle during pregnancy.

Possible signs and symptoms of heart and blood vessel late effects include trouble breathing and chest pain.

These and other signs and symptoms may be caused by heart and blood vessel late effects or by other conditions:

• Trouble breathing, especially when lying down.
• Heartbeat that is too slow, too fast, or different from the heart's normal rhythm.
• Chest pain or pain in the arm or leg.
• Swelling of the feet, ankles, legs, or abdomen.
• When exposed to cold or having strong emotions, the fingers, toes, ears, or nose become white and then turn blue. When this happens to the fingers, there may also be pain and tingling.
• Sudden numbness or weakness of the face, arm, or leg (especially on one side of the body).
• Sudden confusion or trouble speaking or understanding speech.
• Sudden trouble seeing with one or both eyes.
• Sudden trouble walking or feeling dizzy.
• Sudden loss of balance or coordination.
• Sudden severe headache for no known reason.
• Pain, warmth, or redness in one area of the arm or leg, especially the back of the lower leg.

Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the heart and blood vessels.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Electrocardiogram (EKG): A recording of the heart's electrical activity to check its rate and rhythm. A number of small pads (electrodes) are placed on the patient's chest, arms, and legs, and are connected by wires to the EKG machine. Heart activity is then recorded as a line graph on paper. Electrical activity that is faster or slower than normal may be a sign of heart disease or damage.
• Echocardiogram: A procedure in which high-energy sound waves (ultrasound) are bounced off the heart and nearby tissues or organs and make echoes. A moving picture is made of the heart and heart valves as blood is pumped through the heart.
• Ultrasound exam: A procedure in which high-energy sound waves (ultrasound) are bounced off internal tissues or organs such as the heart and make echoes. The echoes form a picture of body tissues called a sonogram. The picture can be printed to be looked at later.
• MRI (magnetic resonance imaging): A procedure that uses a magnet, radio waves, and a computer to make a series of detailed pictures of areas inside the body. This procedure is also called nuclear magnetic resonance imaging (NMRI). This procedure is done to check for blood clots.
• CT scan (CAT scan): A procedure that makes a series of detailed pictures of areas inside the body, taken from different angles. The pictures are made by a computer linked to an x-ray machine. A dye may be injected into a vein or swallowed to help the organs or tissues show up more clearly. This procedure is also called computed tomography, computerized tomography, or computerized axial tomography. This procedure is done to check for blood clots.
• MRA (magnetic resonance angiography): A procedure that uses radio waves and a powerful magnet linked to a computer to create detailed pictures of the blood vessels and blood flow inside the body. A dye may be injected into a vein to make the blood vessels and blood flow easier to see. This may be used to check for blood clots or other blood vessel problems.
• Lipid profile studies: A procedure in which a blood sample is checked to measure the amounts of triglycerides, cholesterol, and low- and high-density lipoprotein cholesterol in the blood.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of heart and blood vessel late effects. If tests are needed, find out how often they should be done.

Health habits that promote a healthy heart and blood vessels are important for survivors of childhood cancer.

Childhood cancer survivors may lower their risk of heart and blood vessel late effects by having a healthy lifestyle, which includes:

• A healthy weight.
• A heart-healthy diet.
• Regular exercise.
• Not smoking.

Central Nervous System

Brain and spinal cord late effects are more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause brain and spinal cord late effects:

• Acute lymphoblastic leukemia (ALL).
• Acute myeloid leukemia (AML).
• Brain and spinal cord tumors.
• Head and neck cancers, including retinoblastoma.
• Hodgkin lymphoma.
• Non-Hodgkin lymphoma.
• Osteosarcoma.
• Soft tissue sarcoma.

Radiation to the brain increases the risk of brain and spinal cord late effects.

The risk of health problems that affect the brain or spinal cord increases after treatment with the following:

• Radiation to the brain or spinal cord, especially high doses of radiation. This includes total-body irradiation given as part of a stem cell transplant.
• Intrathecal or intraventricular chemotherapy.
• Chemotherapy with high-dose methotrexate or cytarabine that can cross the blood-brain barrier (protective lining around the brain). This includes high-dose chemotherapy given as part of a stem cell transplant.
• Surgery to remove a tumor on the brain or spinal cord.

When radiation to the brain and intrathecal chemotherapy are given at the same time, the risk of late effects is higher.

The following may also increase the risk of brain and spinal cord late effects in childhood brain tumor survivors:

• Being about 5 years old or younger at the time of treatment.
• Being female.
• Having hydrocephalus and a shunt placed to remove the extra fluid from the ventricles.
• Having hearing loss.
• Having cerebellar mutism following surgery to remove the brain tumor. Cerebellar mutism includes not being able to speak, having trouble swallowing and eating, loss of coordination and balance, mood swings, being irritable, and having a high-pitched cry.
• Having a personal history of stroke.
• Seizures.

Central nervous system late effects are also affected by where the tumor has formed in the brain and spinal cord.

Late effects that affect the brain and spinal cord may cause certain health problems.

Childhood cancer survivors who received radiation, certain types of chemotherapy, or surgery to the brain or spinal cord have an increased risk of late effects to the brain and spinal cord and related health problems. These include the following:

• Headaches that may go away after vomiting.
• Loss of balance, lack of coordination, or trouble walking.
• Dizziness.
• Seizures.
• Loss of the myelin sheath that covers nerve fibers in the brain.
• Movement disorders that affect the legs and eyes or the ability to speak and swallow.
• Nerve damage in the hands or feet.
• Stroke. A second stroke may be more likely in survivors who received radiation to the brain, have a history of high blood pressure, or were older than 40 years when they had their first stroke.
• Daytime sleepiness.
• Hydrocephalus.
• Loss of bladder and/or bowel control.
• Cavernomas (clusters of abnormal blood vessels).
• Back pain.

Survivors may also have late effects that affect thinking, learning, memory, emotions, and behavior.

New ways of using more targeted and lower doses of radiation to the brain may lessen the risk of brain and spinal cord late effects.

Possible signs and symptoms of brain and spinal cord late effects include headaches, loss of coordination, and seizures.

These signs and symptoms may be caused by brain and spinal cord late effects or by other conditions:

• Trouble speaking or swallowing.
• Trouble with having the eyes work together.
• Numbness, tingling, or weakness in the hands or feet.
• Being unable to bend the ankle to lift the foot up.
• Sudden numbness or weakness of the face, arm, or leg (especially on one side of the body).
• Unusual sleepiness or change in activity level.
• Unusual changes in personality or behavior.
• A change in bowel habits or trouble urinating.
• Increase in head size (in infants).
• Sudden confusion or trouble speaking or understanding speech.
• Sudden trouble seeing with one or both eyes.
• Sudden severe headache for no known reason.

Other signs and symptoms include the following:

• Problems with memory.
• Problems with paying attention.
• Trouble with solving problems.
• Trouble with organizing thoughts and tasks.
• Slower ability to learn and use new information.
• Trouble learning to read, write, or do math.
• Trouble coordinating movement between the eyes, hands, and other muscles.
• Delays in normal development.
• Social withdrawal or trouble getting along with others.

Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the brain and spinal cord.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Neurological exam: A series of questions and tests to check the brain, spinal cord, and nerve function. The exam checks a person's mental status, coordination, and ability to walk normally, and how well the muscles, senses, and reflexes work. This may also be called a neuro exam or a neurologic exam. In some cases, a more complete exam may be done by a neurologist or neurosurgeon.
• Neuropsychological assessment: A series of tests to examine the patient's mental processes and behavior. Areas that are checked usually include:
  • Knowing who and where you are and what day it is.
  • Ability to learn and remember new information.
  • Intelligence.
  • Ability to solve problems.
  • Use of spoken and written language.
  • Eye-hand coordination.
  • Ability to organize information and tasks.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of brain and spinal cord late effects. If tests are needed, find out how often they should be done.

Survivors of childhood cancer may have anxiety and depression related to their cancer.

Survivors of childhood cancer may have anxiety and depression related to physical changes, having pain, the way they look, or the fear of cancer coming back. These and other factors may cause problems with personal relationships, education, employment, and health, and cause thoughts of suicide. Survivors with these problems may be less likely to live on their own as adults.

Follow-up exams for childhood cancer survivors should include screening and treatment for possible psychological distress, such as anxiety, depression, and thoughts of suicide.

For more information about psychological distress and coping skills for cancer patients, see the following PDQ summaries:

• Adjustment to Cancer: Anxiety and Distress
• Depression

Some childhood cancer survivors have post-traumatic stress disorder.

Being diagnosed and treated for a life-threatening disease may be traumatic. This trauma may cause post-traumatic stress disorder (PTSD). PTSD is defined as having certain behaviors following a stressful event that involved death or the threat of death, serious injury, or a threat to oneself or others.

PTSD can affect cancer survivors in the following ways:

• Reliving the time they were diagnosed and treated for cancer, in nightmares or flashbacks, and thinking about it all the time.
• Avoiding places, events, and people that remind them of the cancer experience.

In general, childhood cancer survivors show low levels of PTSD, depending in part on the coping style of patients and their parents. Survivors who received radiation therapy to the head when younger than 4 years or survivors who received intensive treatment may be at higher risk of PTSD. Family problems, little or no social support from family or friends, and stress not related to the cancer may increase the chances of having PTSD.

Because avoiding places and persons connected to the cancer may be part of PTSD, survivors with PTSD may not get the medical treatment they need.

Adolescents who are diagnosed with cancer may have social problems later in life.

Adolescents who are diagnosed with cancer may reach fewer social milestones or reach them later in life than adolescents not diagnosed with cancer. Social milestones include having a first boyfriend or girlfriend, getting married, and having a child. They may also have trouble getting along with other people or feel like they are not liked by others their age.

Cancer survivors in this age group have reported being less satisfied with their health and their lives in general compared with others of the same age who did not have cancer. Adolescents and young adults who survived cancer need special programs that give psychological, educational, and job support.

Digestive System

Teeth and jaws

Problems with the teeth and jaws are late effects that are more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause the late effect of problems with teeth and jaws:

• Head and neck cancers.
• Hodgkin lymphoma.
• Neuroblastoma.
• Leukemia that spreads to the brain and spinal cord.
• Nasopharyngeal cancer.
• Brain tumors.
• Cancers treated with total-body irradiation (TBI) as part of a stem cell transplant.

Radiation to the head and neck and certain types of chemotherapy increase the risk of late effects to the teeth and jaws.

The risk of health problems that affect the teeth and jaws increases after treatment with the following:

• Radiation therapy to the head and neck.
• TBI as part of a stem cell transplant.
• Chemotherapy, especially with higher doses of alkylating agents such as cyclophosphamide.
• Surgery in the head and neck area.

Risk is also increased in survivors who were younger than 5 years at the time of treatment because their permanent teeth had not fully formed.

Late effects that affect the teeth and jaws may cause certain health problems.

Teeth and jaws late effects and related health problems include the following:

• Teeth that are not normal.
• Tooth decay (including cavities) and gum disease.
• Salivary glands do not make enough saliva.
• Death of the bone cells in the jaw.
• Changes in the way the face, jaw, or skull form.

Possible signs and symptoms of late effects of the teeth and jaws include tooth decay (cavities) and jaw pain.

These and other signs and symptoms may be caused by late effects of the teeth and jaws or by other conditions:

• Teeth are small or do not have a normal shape.
• Missing permanent teeth.
• Permanent teeth come in at a later than normal age.
• Teeth have less enamel than normal.
• More tooth decay (cavities) and gum disease than normal.
• Dry mouth.
• Trouble chewing, swallowing, and speaking.
• Jaw pain.
• Jaws do not open and close the way they should.

Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the mouth and jaws.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Dental exam: An exam of the teeth, mouth, and jaws to check general signs of dental health, including checking for signs of disease, such as cavities or anything that seems unusual.This may also be called a dental check-up.
• Panorex x-ray: An x-ray of all of the teeth and their roots. An x-ray is a type of energy beam that can go through the body and onto film, making a picture of areas inside the body.
• X-ray of the jaws: An x-ray of the jaws. An x-ray is a type of energy beam that can go through the body and onto film, making a picture of areas inside the body.
• CT scan (CAT scan): A procedure that makes a series of detailed pictures of areas inside the body, such as the head and neck, taken from different angles. The pictures are made by a computer linked to an x-ray machine. This procedure is also called computed tomography, computerized tomography, or computerized axial tomography.
• MRI (magnetic resonance imaging): A procedure that uses a magnet, radio waves, and a computer to make a series of detailed pictures of areas inside the body, such as the head and neck. This procedure is also called nuclear magnetic resonance imaging (NMRI).
• Biopsy: The removal of bone cells from the jaw so they can be viewed under a microscope to check for signs of bone death after radiation therapy.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of teeth and jaw late effects. If tests are needed, find out how often they should be done.

Regular dental care is very important for survivors of childhood cancer.

Doctors suggest that survivors of childhood cancer have a dental check-up and a cleaning and fluoride treatment every 6 months. Children who had radiation therapy to the oral cavity may also see an orthodontist or an otolaryngologist. If lesions are present in the mouth, a biopsy may be needed.

Digestive tract

Digestive tract late effects are more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause late effects of the digestive tract (esophagus, stomach, small and large intestines, rectum and anus):

• Germ cell tumors.
• Hodgkin lymphoma.
• Non-Hodgkin lymphoma.
• Neuroblastoma.
• Rhabdomyosarcoma of the bladder or prostate, or near the testicles.
• Wilms tumor.

Radiation to the bladder, prostate, or testicles and certain types of chemotherapy increase the risk of digestive tract late effects.

The risk of health problems that affect the digestive tract increases after treatment with the following:

• Radiation therapy to the abdomen or areas near the abdomen, such as the esophagus, bladder, prostate, or testicles, may cause digestive tract problems that begin quickly and last for a short time. In some patients, however, digestive tract problems are delayed and long-lasting. These late effects are caused by radiation therapy that damages the blood vessels. Receiving higher doses of radiation therapy or receiving chemotherapy such as dactinomycin or anthracyclines together with radiation therapy may increase this risk.
• Abdominal surgery or pelvic surgery to remove the bladder.
• Chemotherapy with alkylating agents such as cyclophosphamide, procarbazine, and ifosfamide, or with anthracyclines such as doxorubicin, daunorubicin, idarubicin, and epirubicin.
• Stem cell transplant.

The following may also increase the risk of digestive tract late effects:

• Older age at diagnosis or when treatment begins.
• Treatment with both radiation therapy and chemotherapy.
• A history of chronic graft-versus-host disease.

Late effects that affect the digestive tract may cause certain health problems.

Digestive tract late effects and related health problems include the following:

• A narrowing of the esophagus or intestine.
• The muscles of the esophagus do not work well.
• Reflux.
• Diarrhea, constipation, fecal incontinence, or blocked bowel.
• Bowel perforation (a hole in the intestine).
• Inflammation of the intestines.
• Death of part of the intestine.
• Intestine is not able to absorb nutrients from food.

Possible signs and symptoms of digestive tract late effects include abdominal pain and diarrhea.

These and other signs and symptoms may be caused by digestive tract late effects or by other conditions:

• Trouble swallowing or feeling like food is stuck in the throat.
• Heartburn.
• Fever with severe pain in the abdomen and nausea.
• Pain in the abdomen.
• A change in bowel habits (constipation or diarrhea).
• Nausea and vomiting.
• Frequent gas pains, bloating, fullness, or cramps.
• Reflux.

Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the digestive tract.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Digital rectal exam: An exam of the rectum. The doctor or nurse inserts a lubricated, gloved finger into the rectum to feel for lumps or anything else that seems unusual.
• Blood chemistry studies: A procedure in which a blood sample is checked to measure the amounts of certain substances released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease.
• Kidney, ureter, and bladder x-ray: An x-ray is a type of energy beam that can go through the body and onto film, making a picture of areas inside the body. An x-ray may be taken of the abdomen, kidney, ureter, or bladder to check for signs of disease.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of digestive tract late effects. If tests are needed, find out how often they should be done.

Liver and bile ducts

Liver and bile duct late effects are more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause liver or bile duct late effects:

• Acute lymphoblastic leukemia (ALL).
• Liver cancer.
• Wilms tumor.
• Cancers treated with a stem cell transplant.

Certain types of chemotherapy and radiation to the liver or bile ducts increase the risk of late effects.

The risk of liver or bile duct late effects may be increased in childhood cancer survivors treated with one of the following:

• Surgery to remove part of the liver or a liver transplant.
• Chemotherapy that includes high-dose cyclophosphamide as part of a stem cell transplant.
• Chemotherapy such as 6-mercaptopurine, 6-thioguanine, methotrexate, and dactinomycin.
• Radiation therapy to the liver and bile ducts. The risk depends on the following:
  • The dose of radiation and how much of the liver is treated.
  • Age when treated (the younger the age, the higher the risk).
  • Whether there was surgery to remove part of the liver.
  • Whether chemotherapy, such as doxorubicin or dactinomycin, was given together with radiation therapy.
• Stem cell transplant.

The following may also increase the risk of liver and bile duct late effects:

• Hepatitis B or hepatitis C infection.
• History of chronic graft-versus-host disease.
• Liver damage caused by veno-occlusive disease /sinusoidal obstruction syndrome.
• Tissue and organ damage from the buildup of extra iron after having many blood transfusions.

Late effects that affect the liver and bile ducts may cause certain health problems.

Liver and bile duct late effects and related health problems include the following:

• Liver doesn't work the way it should or stops working.
• Gallstones.
• Benign liver lesions.
• Liver fibrosis (an overgrowth of connective tissue in the liver) or cirrhosis.
• Fatty liver with insulin resistance (a condition in which the body makes insulin but cannot use it well).

Possible signs and symptoms of liver and bile duct late effects include abdominal pain and jaundice.

These and other signs and symptoms may be caused by liver and bile duct late effects or by other conditions:

• Weight gain or weight loss.
• Swelling of the abdomen.
• Nausea and vomiting.
• Pain in the abdomen. Pain may occur near the ribs, often on the right side, or after eating a fatty meal.
• Jaundice (yellowing of the skin and whites of the eyes).
• Light-colored bowel movements.
• Diarrhea.
• Dark-colored urine.
• A lot of gas.
• Lack of appetite.
• Feeling tired or weak.

Talk to your child's doctor if your child has any of these problems.

Sometimes there are no signs or symptoms of liver or bile duct late effects and treatment may not be needed.

Certain tests and procedures are used to diagnose health problems in the liver and bile duct.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Blood chemistry studies: A procedure in which a blood sample is checked to measure the amounts of certain substances released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease For example, there may be a higher level of bilirubin, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) in the body if the liver has been damaged.
• Ferritin level: A procedure in which a blood sample is checked to measure the amount of ferritin. Ferritin is a protein that binds to iron and stores it for use by the body. After a stem cell transplant, a high ferritin level may be a sign of liver disease.
• Complete blood count (CBC): A test in which a sample of blood is drawn and checked for the following:
  • The number of red blood cells, white blood cells, and platelets.
  • The amount of hemoglobin (the protein that carries oxygen) in the red blood cells.
  • The portion of the blood sample made up of red blood cells.

  This test is used to check the amount of platelets in the body.

• Prothrombin time (PT) test: A test that measures how long it takes for the blood to clot.
• Hepatitis assay: A procedure in which a blood sample is checked for pieces of the hepatitis virus. The blood sample may also be used to measure how much hepatitis virus is in the blood. All patients who had a blood transfusion before 1972 should have a screening test for hepatitis B. Patients who had a blood transfusion before 1993 should have a screening test for hepatitis C.
• Ultrasound exam: A procedure in which high-energy sound waves (ultrasound) are bounced off internal tissues or organs, such as the gall bladder, and make echoes. The echoes form a picture of body tissues called a sonogram. The picture can be printed to be looked at later.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of liver or bile duct late effects. If tests are needed, find out how often they should be done.

Health habits that promote a healthy liver are important for survivors of childhood cancer.

Childhood cancer survivors with liver late effects should take care to protect their health, including:

• Having a healthy weight.
• Not drinking alcohol.
• Getting vaccines for hepatitis A and hepatitis B viruses.

Pancreas

Radiation therapy increases the risk of pancreatic late effects.

The risk of pancreatic late effects may be increased in childhood cancer survivors after treatment with one of the following:

• Radiation therapy to the abdomen.
• Total-body irradiation as part of a stem cell transplant.

Late effects that affect the pancreas may cause certain health problems.

Pancreatic late effects and related health problems include the following:

• Insulin resistance: A condition in which the body does not use insulin the way it should. Insulin is needed to help control the amount of glucose (a type of sugar) in the body. Because the insulin does not work the way it should, glucose and fat levels rise.
• Diabetes mellitus: A disease in which the body does not make enough insulin or does not use it the way it should. When there is not enough insulin, the amount of glucose in the blood increases and the kidneys make a large amount of urine.

Possible signs and symptoms of pancreatic late effects include frequent urination and being thirsty.

These and other signs and symptoms may be caused by pancreatic late effects or by other conditions:

• Frequent urination.
• Feeling very thirsty.
• Feeling very hungry.
• Weight loss for no known reason.
• Feeling very tired.
• Frequent infections, especially of the skin, gums, or bladder.
• Blurred vision.
• Cuts or bruises that are slow to heal.
• Numbness or tingling in the hands or feet.

Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the pancreas.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Glycated hemoglobin (A1C) test: A procedure in which a sample of blood is drawn and the amount of glucose that is attached to red blood cells is measured. A higher-than-normal amount of glucose attached to red blood cells can be a sign of diabetes mellitus.
• Fasting blood sugar test: A test in which a blood sample is checked to measure the amount of glucose in the blood. This test is done after the patient has had nothing to eat overnight. A higher than normal amount of glucose in the blood can be a sign of diabetes mellitus.

Endocrine System

Thyroid gland

Thyroid late effects are more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause thyroid late effects:

• Acute lymphoblastic leukemia (ALL).
• Brain tumors.
• Head and neck cancers.
• Hodgkin lymphoma.
• Neuroblastoma.
• Cancers treated with a stem cell transplant.

Radiation therapy to the head and neck increases the risk of thyroid late effects.

The risk of thyroid late effects may be increased in childhood cancer survivors after treatment with any of the following:

• Radiation therapy to the thyroid as part of radiation therapy to the head and neck or to the pituitary gland in the brain.
• Total-body irradiation as part of a stem cell transplant.
• MIBG (radioactive iodine) therapy for neuroblastoma.
• Chemotherapy such as alkylating agents, anthracyclines, or bleomycin.

The risk also is increased in females, in survivors who were a young age at the time of treatment, in survivors who had a higher radiation dose, and as the time since diagnosis and treatment gets longer.

Late effects that affect the thyroid may cause certain health problems.

Thyroid late effects and related health problems include the following:

• Hypothyroidism (not enough thyroid hormone): There is a higher risk of hypothyroidism in survivors treated with head and neck radiation involving the thyroid gland, especially survivors of Hodgkin lymphoma. This is the most common thyroid late effect. It usually occurs 2 to 5 years after treatment ends but may occur longer than 25 years after radiation therapy. It is more common in girls than boys.
• Hyperthyroidism (too much thyroid hormone): The risk of hyperthyroidism increases with higher doses of radiation therapy to the thyroid gland. Hyperthyroidism is less common than hypothyroidism. It usually occurs 5 years after treatment ends, but may occur longer than 25 years after radiation therapy.
• Goiter (an enlarged thyroid).
• Lumps in the thyroid: Higher radiation dose and longer time since diagnosis are linked to an increased risk of developing thyroid lumps. These growths may be benign (not cancerous) or malignant (cancer). It is more common in girls than boys.

Signs and symptoms of thyroid late effects depend on whether there is too little or too much thyroid hormone in the body.

These and other signs and symptoms may be caused by thyroid late effects or by other conditions:

Hypothyroidism (too little thyroid hormone)

• Feeling tired or weak.
• Being more sensitive to cold.
• Pale, dry skin.
• Coarse and thinning hair.
• Brittle fingernails.
• Hoarse voice.
• Puffy face.
• Muscle and joint aches and stiffness.
• Constipation.
• Menstrual periods that are irregular or heavier than normal.
• Weight gain for no known reason.
• Depression or trouble with memory or being able to concentrate.

Rarely, hypothyroidism does not cause any symptoms.

Hyperthyroidism (too much thyroid hormone)

• Feeling nervous, anxious, or moody.
• Trouble sleeping.
• Feeling tired or weak.
• Having shaky hands.
• Having a fast heartbeat.
• Having red, warm skin that may be itchy.
• Having fine, soft hair that is falling out.
• Having frequent or loose bowel movements.
• Weight loss for no known reason.
• Being more sensitive to heat.

Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the thyroid.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Blood hormone studies: A procedure in which a blood sample is checked to measure the amounts of certain hormones released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease in the organ or tissue that makes it. The blood may be checked for abnormal levels of thyroid-stimulating hormone (TSH) or free thyroxine (T4).
• Ultrasound exam: A procedure in which high-energy sound waves (ultrasound) are bounced off internal tissues or organs and make echoes. The echoes form a picture of body tissues called a sonogram. The picture can be printed to be looked at later. This procedure can show the size of the thyroid and whether there are nodules (lumps) on the thyroid.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of thyroid late effects. If tests are needed, find out how often they should be done.

Hypothalamus and pituitary gland

Neuroendocrine late effects may be caused after treatment for certain childhood cancers.

The neuroendocrine system is the nervous system and the endocrine system working together.

Treatment for these and other childhood cancers may cause neuroendocrine late effects:

• Acute lymphoblastic leukemia (ALL).
• Brain and spinal cord tumors.
• Cancers treated with total-body irradiation (TBI) before a stem cell transplant.

Treatment that affects the hypothalamus or pituitary gland increases the risk of neuroendocrine system late effects.

Childhood cancer survivors have an increased risk for neuroendocrine late effects. These effects are caused by radiation therapy to the brain in the area of the hypothalamus. The hypothalamus controls the way hormones are made and released into the bloodstream by the pituitary gland. Radiation therapy may be given to treat cancer near the hypothalamus or as total-body irradiation before a stem cell transplant. These effects are also caused by surgery in the area of the hypothalamus, pituitary gland, or optic pathways.

Childhood cancer survivors who have neuroendocrine late effects may have low levels of any of the following hormones made in the pituitary gland and released into the blood:

• Growth hormone (helps promote growth and control metabolism).
• Adrenocorticotropic hormone (ACTH; controls the making of glucocorticoids).
• Prolactin (controls the making of breast milk).
• Thyroid-stimulating hormone (TSH; controls the making of thyroid hormones).
• Luteinizing hormone (LH; controls reproduction).
• Follicle-stimulating hormone (FSH; controls reproduction).

Late effects that affect the hypothalamus may cause certain health problems.

Neuroendocrine late effects and related health problems include the following:

• Growth hormone deficiency: A low level of growth hormone is a common late effect of radiation to the brain in childhood cancer survivors. The higher the radiation dose and the longer the time since treatment, the greater the risk of this late effect. A low level of growth hormone may also occur in childhood ALL and stem cell transplant survivors who received radiation therapy to the brain and spinal cord and/or chemotherapy.

  A low level of growth hormone in childhood results in adult height that is shorter than normal. If the child's bones have not fully developed, low growth hormone levels may be treated with growth hormone replacement therapy beginning one year after the end of treatment.

• Adrenocorticotropin deficiency: A low level of adrenocorticotropic hormone is an uncommon late effect. It may occur in childhood brain tumor survivors, survivors with low growth hormone levels or central hypothyroidism, or after radiation therapy to the brain.

  Symptoms of deficiency may not be severe and may not be noticed. Signs and symptoms of adrenocorticotropin deficiency include the following:

  • Weight loss for no known reason.
  • Not feeling hungry.
  • Nausea.
  • Vomiting.
  • Abdominal pain.
  • Low blood pressure.
  • Feeling tired.
  • Dizziness.

  Low levels of adrenocorticotropin may be treated with hydrocortisone therapy.

• Hyperprolactinemia: A high level of the hormone prolactin may occur after a high dose of radiation to the brain or surgery that affects part of the pituitary gland. A high level of prolactin may cause the following:
  • Puberty at a later age than normal.
  • Flow of breast milk in a woman who is not pregnant or breast-feeding.
  • Less frequent or no menstrual periods or menstrual periods with a very light flow.
  • Hot flashes.
  • Inability to become pregnant.
  • Inability to have an erection needed for sexual intercourse.
  • Lower sex drive (in men and women).
  • Osteopenia (low bone mineral density).

  Sometimes there are no signs and symptoms. Treatment is rarely needed.

• Thyroid-stimulating hormone deficiency (central hypothyroidism): A low level of thyroid hormone may occur very slowly over time after radiation therapy to the brain.

  Sometimes the symptoms of thyroid-stimulating hormone deficiency are not noticed. Low thyroid hormone levels may cause slow growth and delayed puberty, as well as other symptoms. A low level of thyroid hormone may be treated with thyroid hormone replacement therapy.

• Luteinizing hormone or follicle-stimulating hormone deficiency: Low levels of these hormones can cause different health problems. The type of problem depends on the radiation dose.

  Childhood cancer survivors who were treated with lower doses of radiation to the brain may develop central precocious puberty (a condition that causes puberty to start before age 8 in girls and 9 in boys). This condition may be treated with gonadotropin-releasing hormone (GnRH) agonist therapy to delay puberty and help the child's growth. Hydrocephalus may also increase the risk of this late effect.

  Childhood cancer survivors who were treated with higher doses of radiation to the brain may have low levels of luteinizing hormone or follicle-stimulating hormone. This condition may be treated with sex hormone replacement therapy. The dose will depend on the child's age and whether the child has reached puberty.

• Central diabetes insipidus: Central diabetes insipidus may be caused by the absence of or low amounts of all of the hormones made in the front part of the pituitary gland and released into the blood. It may occur in childhood cancer survivors treated with surgery in the area of the hypothalamus or pituitary gland. Signs and symptoms of central diabetes insipidus may include the following:
  • Producing large amounts of urine.
  • Feeling very thirsty.
  • Fatigue.
  • Slowed growth and development.
  • Weight loss for no known reason.

Certain tests and procedures are used to diagnose health problems in the neuroendocrine system.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Blood chemistry study: A procedure in which a blood sample is checked to measure the amounts of certain substances, such as glucose, released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease.
• Blood hormone studies: A procedure in which a blood sample is checked to measure the amounts of certain hormones released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease in the organ or tissue that makes it. The blood may be checked for abnormal levels of follicle-stimulating hormone, luteinizing hormone, estradiol, testosterone, cortisol, or free thyroxine (T4).
• Lipid profile studies: A procedure in which a blood sample is checked to measure the amounts of triglycerides, cholesterol, and low- and high-density lipoprotein cholesterol in the blood.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of neuroendocrine late effects. If tests are needed, find out how often they should be done.

Testicles and ovaries

For information about late effects in the testicles and ovaries, see the Reproductive System section.

Metabolic syndrome

Metabolic syndrome is more likely to occur after treatment for certain childhood cancers.

Metabolic syndrome is a group of medical conditions that includes having too much fat around the abdomen and at least two of the following:

• High blood pressure.
• High levels of triglycerides and low levels of high-density lipoprotein (HDL) cholesterol in the blood.
• High levels of glucose (sugar) in the blood.

Treatment for these and other childhood cancers may cause metabolic syndrome to occur later in life:

• Acute lymphoblastic leukemia (ALL).
• Cancers treated with a stem cell transplant.
• Cancers treated with radiation to the abdomen, such as Wilms tumor or neuroblastoma.

Radiation therapy increases the risk of metabolic syndrome.

The risk of metabolic syndrome may be increased in childhood cancer survivors after treatment with any of the following:

• Radiation therapy to the brain, abdomen, or pelvis.
• Total-body irradiation (TBI) as part of a stem cell transplant.
• Chemotherapy, such as alkylating agents.
• Older age.

Certain tests and procedures are used to diagnose metabolic syndrome.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Blood chemistry studies: A procedure in which a blood sample is checked to measure the amounts of certain substances, such as glucose, released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease.
• Lipid profile studies: A procedure in which a blood sample is checked to measure the amounts of triglycerides, cholesterol, and low- and high-density lipoprotein cholesterol in the blood.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of metabolic syndrome. If tests are needed, find out how often they should be done.

Metabolic syndrome may cause heart and blood vessel disease and diabetes.

Metabolic syndrome is linked to an increased risk of heart and blood vessel disease and diabetes. Health habits that decrease these risks include:

• Having a healthy weight.
• Eating a heart-healthy diet.
• Having regular exercise.
• Not smoking.

Weight

Being underweight, being overweight, or having obesity is a late effect that is more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause a change in weight:

• Acute lymphoblastic leukemia (ALL).
• Brain tumors, especially craniopharyngiomas.
• Cancers treated with radiation to the brain, including TBI as part of a stem cell transplant.

Graft-versus-host disease may also cause a change in weight for patients treated with a stem cell transplant.

Radiation therapy increases the risk of being underweight, being overweight, or having obesity.

The risk of being underweight increases after treatment with the following:

• TBI for females.
• Radiation therapy to the abdomen for males.
• Certain types of chemotherapy (alkylating agents and anthracyclines).

The risk of being overweight or having obesity increases after treatment with the following:

• Radiation therapy to the brain.
• Surgery that damages the hypothalamus or pituitary gland, such as surgery to remove a craniopharyngioma brain tumor.

The following may also increase the risk of obesity:

• Being diagnosed with cancer between the ages of 5 and 9.
• Being female.
• Having growth hormone deficiency or low levels of the hormone leptin.
• Not doing enough physical activity to stay at a healthy body weight.
• Taking an antidepressant called paroxetine.

Childhood cancer survivors who get enough exercise and have a normal amount of anxiety have a lower risk of obesity.

Certain tests and procedures are used to diagnose a change in weight.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Blood chemistry studies: A procedure in which a blood sample is checked to measure the amounts of certain substances, such as glucose, released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease.
• Lipid profile studies: A procedure in which a blood sample is checked to measure the amounts of triglycerides, cholesterol, and low- and high-density lipoprotein cholesterol in the blood.

Being underweight, being overweight, or having obesity may be measured by weight, body mass index, percent of body fat, or size of the abdomen (belly fat).

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of a change in weight. If tests are needed, find out how often they should be done.

Immune System

Surgery to remove the spleen increases the risk of immune system late effects.

The risk of health problems that affect the immune system increases after treatment with the following:

• Surgery to remove the spleen.
• High-dose radiation therapy to the spleen that causes the spleen to stop working.
• Stem cell transplant followed by graft-versus-host disease that causes the spleen to stop working.

Late effects that affect the immune system may cause infection.

Late effects that affect the immune system may increase the risk of very serious bacterial infections. This risk is higher in younger children than in older children and may be greater in the early years after the spleen stops working or is removed by surgery. These signs and symptoms may be caused by infection:

• Redness, swelling, or warmth of a part of the body.
• Pain that is in one part of the body, such as the eye, ear, or throat.
• Fever.

An infection may cause other symptoms that depend on the part of the body affected. For example, a lung infection may cause a cough and trouble breathing.

Children who have had their spleen removed may need antibiotics to lessen the risk of infection.

Daily antibiotics may be prescribed for children younger than 5 whose spleen is no longer working or for at least 1 year after surgery to remove the spleen. For certain high-risk patients, daily antibiotics may be prescribed throughout childhood and into adulthood.

In addition, children with an increased risk of infection should be vaccinated on a schedule through adolescence against the following:

• Pneumococcal disease.
• Meningococcal disease.
• Haemophilus influenzae type b (Hib) disease.
• Diphtheria-tetanus-pertussis (DTaP).
• Hepatitis B.

Talk to your child's doctor about whether other childhood vaccinations given before cancer treatment need to be repeated.

Musculoskeletal System

Bone and joint late effects are more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause bone and joint late effects:

• Acute lymphoblastic leukemia (ALL).
• Bone cancer.
• Brain and spinal cord tumors.
• Ewing sarcoma.
• Head and neck cancers.
• Neuroblastoma.
• Non-Hodgkin lymphoma.
• Osteosarcoma.
• Retinoblastoma.
• Soft tissue sarcoma, such as rhabdomyosarcoma.
• Wilms tumor.
• Cancers treated with a stem cell transplant.

Poor nutrition and not enough exercise may also cause bone late effects.

Radiation therapy, surgery, chemotherapy, and other treatments increase the risk of bone and joint late effects.

Radiation therapy

Radiation therapy can stop or slow the growth of bone and muscle. The type of bone and joint late effect depends on the part of the body that received radiation therapy. Radiation therapy may cause any of the following:

• Changes in the way the face or skull form, especially when high-dose radiation with or without chemotherapy is given to children before age 5.
• Short stature (being shorter than normal).
• Scoliosis (curving of the spine) or kyphosis (rounding of the spine).
• One arm or leg is shorter than the other arm or leg.
• Osteoporosis (weak or thin bones that can break easily). Fractures (broken bones) can occur with high-dose radiation therapy.
• Osteoradionecrosis (parts of the bone die from a lack of blood flow, usually affecting the jaw).
• Osteochondroma (a benign tumor of the bone).

Surgery

Amputation or limb-sparing surgery to remove the cancer and prevent it from coming back may cause late effects depending on where the tumor was, age of the patient, and type of surgery. Health problems after amputation or limb-sparing surgery may include:

• Having problems with activities of daily living.
• Not being able to be as active as normal.
• Chronic pain.
• Problems with the way prosthetics fit or work.
• Broken bone.
• The bone may not heal well after surgery.
• One arm or leg is shorter than the other.

Studies show no difference in quality of life in childhood cancer survivors who had amputation compared to those who had limb-sparing surgery.

Chemotherapy and other drug therapy

Risk may be increased in childhood cancer survivors who receive anticancer therapy that includes methotrexate or corticosteroids or glucocorticoids such as dexamethasone. Drug therapy may cause any of the following:

• Osteoporosis (weak or thin bones that can break easily).
• Osteonecrosis (one or more parts of a bone die from a lack of blood flow), especially in the hip or knee.

Stem cell transplant

A stem cell transplant can affect the bone and joints in different ways:

• Total-body irradiation given as part of a stem cell transplant may affect the body's ability to make growth hormone and cause short stature (being shorter than normal). It may also cause osteoporosis (weak or thin bones that can break easily). Osteochondroma (a benign tumor of the long bones, such as the arm or leg bones) may form.
• Chronic graft-versus-host disease may occur after a stem cell transplant and cause joint contractures (tightening of the muscles that causes the joint to shorten and become very stiff). It may also cause osteonecrosis (one or more parts of a bone die from a lack of blood flow).

Possible signs and symptoms of bone and joint late effects include swelling over a bone or bone and joint pain.

These and other signs and symptoms may be caused by bone and joint late effects or by other conditions:

• Swelling over a bone or bony part of the body.
• Pain in a bone or joint.
• Redness or warmth over a bone or joint.
• Joint stiffness or trouble moving normally.
• A bone that breaks easily or for no known reason.
• Short stature (being shorter than normal).
• One side of the body looks higher than the other side or the body tilts to one side.
• Always sitting or standing in a slouching position or having the appearance of a hunched back.

Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the bone and joint.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Bone mineral density scan: An imaging test that measures bone density (the amount of bone mineral in a certain amount of bone) by passing x-rays with two different energy levels through the bone. It is used to diagnose osteoporosis (weak or thin bones that can break easily). Also called BMD scan, DEXA, DEXA scan, dual energy x-ray absorptiometric scan, dual x-ray absorptiometry, and DXA.
• X-ray: An x-ray is a type of energy beam that can go through the body and onto film, making a picture of areas inside the body, such as bones.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of bone and joint late effects. If tests are needed, find out how often they should be done.

Reproductive System

Testicles

Testicular late effects are more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause testicular late effects:

• Acute lymphoblastic leukemia (ALL).
• Ewing sarcoma.
• Germ cell tumors.
• Hodgkin lymphoma.
• Non-Hodgkin lymphoma.
• Rhabdomyosarcoma.
• Soft tissue sarcoma.
• Testicular cancer.
• Cancers treated with a stem cell transplant.

Surgery, radiation therapy, and certain types of chemotherapy increase the risk of late effects that affect the testicles.

The risk of health problems that affect the testicles increases after treatment with one or more of the following:

• Surgery, such as the removal of a testicle, part of the prostate, or lymph nodes in the abdomen.
• Chemotherapy with alkylating agents, such as cyclophosphamide, dacarbazine, procarbazine, and ifosfamide.
• Radiation therapy to the abdomen, pelvis, or in the area of the hypothalamus in the brain.
• Total-body irradiation before a stem cell transplant.

Late effects that affect the testicles may cause certain health problems.

Late effects of the testicles and related health problems include the following:

• Low sperm count: A zero sperm count or a low sperm count may be temporary or permanent. This depends on the radiation dose and schedule, the area of the body treated, and the age when treated.
• Infertility: The inability to father a child.
• Retrograde ejaculation: Very little or no semen comes out of the penis during orgasm.

After treatment with chemotherapy or radiation, the body's ability to make sperm may come back over time.

Certain tests and procedures are used to diagnose health problems in the testicles.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following test.

• Blood hormone studies: A procedure in which a blood sample is checked to measure the amounts of certain hormones released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease in the organ or tissue that makes it. The blood may be checked for abnormal levels of follicle-stimulating hormone, luteinizing hormone, testosterone.

Ovaries

Ovarian late effects are more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause ovarian late effects:

• Acute lymphoblastic leukemia (ALL).
• Germ cell tumors.
• Hodgkin lymphoma.
• Wilms tumor.
• Cancers treated with a stem cell transplant.

Radiation therapy to the abdomen and certain types of chemotherapy increase the risk of ovarian late effects.

The risk of ovarian late effects may be increased after treatment with any of the following:

• Surgery to remove one or both ovaries.
• Chemotherapy with alkylating agents, such as cyclophosphamide, mechlorethamine, cisplatin, ifosfamide, lomustine, busulfan, and especially procarbazine.
• Radiation therapy to the abdomen, pelvis, or lower back. In survivors who had radiation to the abdomen, the damage to the ovaries depends on the radiation dose, age at the time of treatment, and whether all or part of the abdomen received radiation.
• Radiation therapy to the abdomen or pelvis together with alkylating agents.
• Radiation therapy to the area near the hypothalamus in the brain.
• Total-body irradiation before a stem cell transplant.

Late effects that affect the ovaries may cause certain health problems.

Ovarian late effects and other health related problems include the following:

• Early menopause, especially in women who had their ovaries removed or were treated with both an alkylating agent and radiation therapy to the abdomen.
• Changes in menstrual periods.
• Infertility (inability to conceive a child).
• Puberty does not begin.

Possible signs and symptoms of ovarian late effects include irregular or absent menstrual periods and hot flashes.

These and other signs and symptoms may be caused by ovarian late effects or by other conditions:

• Irregular or no menstrual periods.
• Hot flashes.
• Drenching night sweats.
• Trouble sleeping.
• Mood changes.
• Lowered sex drive.
• Vaginal dryness.
• Inability to conceive a child.
• Sex traits, such as developing arm, pubic, and leg hair or having the breasts enlarge, do not occur at puberty.
• Osteoporosis (weak or thin bones that can break easily).

Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the ovaries.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following test.

• Blood hormone studies: A procedure in which a blood sample is checked to measure the amounts of certain hormones released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance can be a sign of disease in the organ or tissue that makes it. The blood may be checked for abnormal levels of follicle-stimulating hormone, luteinizing hormone, or estradiol.

Fertility and reproduction

Treatment for cancer may cause infertility in childhood cancer survivors.

The risk of infertility increases after treatment with the following:

• In boys, treatment with radiation therapy to the testicles.
• In girls, treatment with radiation therapy to the pelvis, including the ovaries and uterus.
• Radiation therapy to an area near the hypothalamus in the brain or lower back.
• Total-body irradiation before a stem cell transplant.
• Chemotherapy with alkylating agents, such as cisplatin, cyclophosphamide, busulfan, lomustine, and procarbazine.
• Surgery, such as the removal of a testicle or an ovary or lymph nodes in the abdomen.

Childhood cancer survivors may have late effects that affect pregnancy.

Late effects on pregnancy include increased risk of the following:

• High blood pressure.
• Diabetes during pregnancy.
• Anemia.
• Miscarriage or stillbirth.
• Low birth-weight babies.
• Early labor and/or delivery.
• Delivery by Cesarean section.
• The fetus is not in the right position for birth (for example, the foot or buttock is in position to come out before the head).

Some studies have not shown an increased risk of late effects on pregnancy.

There are methods that may be used to help childhood cancer survivors have children.

The following methods may be used so that childhood cancer survivors can have children:

• Freezing the eggs or sperm before cancer treatment in patients who have reached puberty.
• Ovarian transposition (preventing damage to the ovaries before radiation therapy by moving one or both ovaries and fallopian tubes out of the field of radiation and attaching them to the wall of the abdomen).
• Testicular sperm extraction (the removal of a small amount of tissue containing sperm from the testicle).
• Intracytoplasmic sperm injection (an egg is fertilized with one sperm that is injected into the egg outside the body).
• In vitro fertilization (IVF) (eggs and sperm are placed together in a container, giving the sperm the chance to enter an egg).

Children of childhood cancer survivors are not affected by the parent's previous treatment for cancer.

The children of childhood cancer survivors do not appear to have an increased risk of birth defects, genetic disease, or cancer.

Respiratory System

Lung late effects are more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause lung late effects:

• Hodgkin lymphoma.
• Wilms tumor.
• Cancers treated with a stem cell transplant.

Certain types of chemotherapy and radiation to the lungs increase the risk of lung late effects.

The risk of health problems that affect the lungs increases after treatment with the following:

• Surgery to remove all or part of the lung or chest wall.
• Chemotherapy. In survivors treated with chemotherapy, such as bleomycin, busulfan, carmustine, or lomustine, and radiation therapy to the chest, there is a high risk of lung damage.
• Radiation therapy to the chest. In survivors who had radiation to the chest, the damage to the lungs and chest wall depends on the radiation dose, whether all or part of the lungs and chest wall received radiation, whether the radiation was given in small, divided daily doses, and the child's age at treatment.
• Total-body irradiation or certain types of chemotherapy before a stem cell transplant.

The risk of lung late effects is greater in childhood cancer survivors who are treated with a combination of surgery, chemotherapy, and/or radiation therapy. The risk is also increased in survivors who have a history of the following:

• Infections or graft-versus-host disease after a stem cell transplant.
• Lung or airway disease, such as asthma, before cancer treatment.
• An abnormal chest wall.
• Smoking cigarettes or other substances.

Late effects that affect the lungs may cause certain health problems.

Lung late effects and related health problems include the following:

• Radiation pneumonitis (inflamed lung caused by radiation therapy).
• Pulmonary fibrosis (the build-up of scar tissue in the lung).
• Other lung and airway problems, such as chronic obstructive pulmonary disease (COPD), pneumonia, pneumothorax, cough that does not go away, and asthma.

Possible signs and symptoms of lung late effects include trouble breathing and cough.

These and other signs and symptoms may be caused by lung late effects or by other conditions:

• Dyspnea (shortness of breath), especially when being active.
• Wheezing.
• Fever.
• Chronic cough.
• Congestion (a feeling of fullness in the lungs from extra mucus).
• Chronic lung infections.
• Feeling tired.

Talk to your child's doctor if your child has any of these problems.

Lung late effects in childhood cancer survivors may occur slowly over time or there may be no symptoms. Sometimes lung damage can be detected only by imaging or pulmonary function testing. Lung late effects may improve over time.

Certain tests and procedures are used to diagnose health problems in the lung.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Chest x-ray: An x-ray of the organs and bones inside the chest. An x-ray is a type of energy beam that can go through the body and onto film, making a picture of areas inside the body.
• Pulmonary function test (PFT): A test to see how well the lungs are working. It measures how much air the lungs can hold and how quickly air moves into and out of the lungs. It also measures how much oxygen is used and how much carbon dioxide is given off during breathing. This is also called lung function test.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of lung late effects. If tests are needed, find out how often they should be done.

Health habits that promote healthy lungs are important for survivors of childhood cancer.

Childhood cancer survivors with lung late effects should take care to protect their health, including:

• Not smoking. Self-help programs and counseling are available to those who want to quit.
• Getting vaccines for flu and pneumococcus.

Senses

Hearing

Hearing problems are a late effect that is more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause hearing late effects:

• Bone cancer.
• Brain tumors.
• Germ cell tumors.
• Head and neck cancers.
• Liver cancer.
• Neuroblastoma.
• Retinoblastoma.
• Soft tissue sarcoma.
• Cancers that are treated with a stem cell transplant.

Radiation therapy to the brain and certain types of chemotherapy increase the risk of hearing loss.

The risk of hearing loss is increased in childhood cancer survivors after treatment with the following:

• Certain types of chemotherapy, such as cisplatin or high-dose carboplatin.
• Radiation therapy to the brain.

The risk of hearing loss is greater in childhood cancer survivors who were young at the time of treatment (the younger the child, the greater the risk), were treated for a brain tumor, or received radiation therapy to the brain and chemotherapy at the same time.

Hearing loss is the most common sign of hearing late effects.

These and other signs and symptoms may be caused by hearing late effects or by other conditions:

• Hearing loss.
• Ringing in the ears.
• Feeling dizzy.
• Too much hardened wax in the ear.

Hearing loss may occur during treatment, soon after treatment ends, or several months or years after treatment ends and worsen over time. Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the ear and hearing problems.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Otoscopic exam: An exam of the ear. An otoscope is used to look at the ear canal and the eardrum to check for signs of infection or hearing loss. Sometimes the otoscope has a plastic bulb that is squeezed to release a small puff of air into the ear canal. In a healthy ear, the eardrum will move. If there is fluid behind the eardrum, it will not move.
• Hearing test: A hearing test can be done in different ways depending on the child's age. The test is done to check if the child can hear soft and loud sounds and low- and high-pitched sounds. Each ear is checked separately. The child may also be asked if he or she can hear the high-pitched hum of a tuning fork when it is placed behind the ear or on the forehead.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of hearing late effects. If tests are needed, find out how often they should be done.

Seeing

Eye and vision problems are a late effect that is more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause eye and vision late effects:

• Acute lymphoblastic leukemia (ALL).
• Brain tumors.
• Head and neck cancers.
• Retinoblastoma, rhabdomyosarcoma, and other tumors of the eye.
• Cancers treated with total-body irradiation (TBI) before a stem cell transplant.

Radiation therapy to the brain or head increases the risk of eye problems or vision loss.

The risk of eye problems or vision loss may be increased in childhood cancer survivors after treatment with any of the following:

• Radiation therapy to the brain, eye, or eye socket.
• Surgery to remove the eye or a tumor near the optic nerve.
• Certain types of chemotherapy, such as cytarabine and doxorubicin or busulfan and corticosteroids as part of a stem cell transplant.
• TBI as part of a stem cell transplant.
• Stem cell transplant (and a history of chronic graft-versus-host disease).

Late effects that affect the eye may cause certain health problems.

Eye late effects and related health problems include the following:

• Having a small eye socket that affects the shape of the child's face as it grows.
• Loss of vision.
• Vision problems, such as cataracts or glaucoma.
• Not being able to make tears.
• Damage to the optic nerve and retina.
• Eyelid tumors.

Possible signs and symptoms of eye and vision late effects include changes in vision and dry eyes.

These and other signs and symptoms may be caused by eye and vision late effects or by other conditions:

• Changes in vision, such as:
  • Not being able to see objects that are close.
  • Not being able to see objects that are far away.
  • Double vision.
  • Cloudy or blurred vision.
  • Colors seem faded.
  • Being sensitive to light or trouble seeing at night.
  • Seeing a glare or halo around lights at night.
• Dry eyes that may feel like they are itchy, burning, or swollen, or like there is something in the eye.
• Eye pain.
• Eye redness.
• Having a growth on the eyelid.
• Drooping of the upper eyelid.

Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the eye and vision problems.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Eye exam with dilated pupil: An exam of the eye in which the pupil is dilated (widened) with medicated eye drops to allow the doctor to look through the lens and pupil to the retina. The inside of the eye, including the retina and the optic nerve, is checked using an instrument that makes a narrow beam of light. This is sometimes called a slit-lamp exam. If there is a tumor, the doctor may take pictures over time to keep track of changes in the size of the tumor and how fast it is growing.
• Indirect ophthalmoscopy: An exam of the inside of the back of the eye using a small magnifying lens and a light.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of eye and vision late effects. If tests are needed, find out how often they should be done.

Urinary System

Kidney

Kidney problems are a late effect that is more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause kidney late effects:

• Sarcoma.
• Wilms tumor.
• Cancers treated with a stem cell transplant.

Certain types of chemotherapy increase the risk of kidney late effects.

The risk of health problems that affect the kidney increases after treatment with the following:

• Chemotherapy including cisplatin, carboplatin, ifosfamide, and methotrexate.
• Radiation therapy to the abdomen or middle of the back.
• Surgery to remove part or all of a kidney.
• Stem cell transplant.

The risk of kidney late effects is greater in childhood cancer survivors who are treated with a combination of surgery, chemotherapy, and/or radiation therapy.

The following may also increase the risk of kidney late effects:

• Having cancer in both kidneys.
• Having a genetic syndrome that increases the risk of kidney problems, such as Denys-Drash syndrome or WAGR syndrome.
• Being treated with more than one type of treatment.

Late effects that affect the kidney may cause certain health problems.

Kidney late effects or related health problems include the following:

• Damage to the parts of the kidney that filter and clean the blood.
• Damage to the parts of the kidney that remove extra water from the blood.
• Loss of electrolytes, such as magnesium, calcium, or potassium, from the body.
• Hypertension (high blood pressure).

Possible signs and symptoms of kidney late effects include problems urinating and swelling of the feet or hands.

These and other signs and symptoms may be caused by kidney late effects or by other conditions:

• Feeling the need to urinate without being able to do so.
• Frequent urination (especially at night).
• Trouble urinating.
• Feeling very tired.
• Swelling of the legs, ankles, feet, face, or hands.
• Itchy skin.
• Shortness of breath.
• Nausea or vomiting.
• Loss of appetite.
• A metal-like taste in the mouth or bad breath.
• Headache.

Sometimes there are no signs or symptoms in the early stages. Signs or symptoms may appear as damage to the kidney continues over time. Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the kidney.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Blood chemistry study: A procedure in which a blood sample is checked to measure the amounts of certain substances, such as magnesium, calcium, and potassium, released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance may be a sign of kidney disease.
• Urinalysis: A test to check the color of urine and its contents, such as sugar, protein, red blood cells, and white blood cells.
• Ultrasound exam: A procedure in which high-energy sound waves (ultrasound) are bounced off internal tissues or organs, such as the kidney, and make echoes. The echoes form a picture of body tissues called a sonogram. The picture can be printed to be looked at later.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of kidney late effects. If tests are needed, find out how often they should be done.

Health habits that promote healthy kidneys are important for survivors of childhood cancer.

Childhood cancer survivors who had all or part of their kidney removed should talk to their doctor about the following:

• Whether it is safe to play sports that have a high risk of heavy contact or impact such as football or hockey.
• Bicycle safety and avoiding handlebar injuries.
• Wearing a seatbelt around the hips, not the waist.

Bladder

Bladder problems are a late effect that is more likely to occur after treatment for certain childhood cancers.

Treatment for these and other childhood cancers may cause bladder late effects:

• Retinoblastoma.
• Cancers treated with a stem cell transplant.

Surgery to the pelvic area and certain types of chemotherapy increase the risk of bladder late effects.

The risk of health problems that affect the bladder increases after treatment with the following:

• Surgery to remove all or part of the bladder.
• Surgery to the pelvis, spine, or brain.
• Certain types of chemotherapy, such as cyclophosphamide or ifosfamide.
• Radiation therapy to areas near the bladder, pelvis, or urinary tract.
• Stem cell transplant.

Late effects that affect the bladder may cause certain health problems.

Bladder late effects and related health problems include the following:

• Hemorrhagic cystitis (inflammation of the inside of the bladder wall, which leads to bleeding).
• Thickening of the bladder wall.
• Decreased urine storage.
• Trouble emptying the bladder.
• Incontinence.
• A blockage in the kidney, ureter, bladder, or urethra.
• Urinary tract infection (chronic).

Possible signs and symptoms of bladder late effects include changes in urination and swelling of the feet or hands.

These and other signs and symptoms may be caused by bladder late effects or by other conditions:

• Feeling the need to urinate without being able to do so.
• Frequent urination (especially at night).
• Trouble urinating.
• Feeling like the bladder does not empty completely after urination.
• Swelling of the legs, ankles, feet, face, or hands.
• Little or no bladder control.
• Blood in the urine.

Talk to your child's doctor if your child has any of these problems.

Certain tests and procedures are used to diagnose health problems in the bladder.

In addition to asking about your child's personal and family health history and doing a physical exam, your child's doctor may perform the following tests and procedures.

• Blood chemistry study: A procedure in which a blood sample is checked to measure the amounts of certain substances, such as magnesium, calcium, and potassium, released into the blood by organs and tissues in the body. An unusual (higher or lower than normal) amount of a substance may be a sign of bladder problems.
• Urinalysis: A test to check the color of urine and its contents, such as sugar, protein, red blood cells, and white blood cells.
• Urine culture: A test to check for bacteria, yeast, or other microorganisms in the urine when there are symptoms of infection. Urine cultures can help identify the type of microorganism that is causing an infection. Treatment of the infection depends on the type of microorganism that is causing the infection.
• Ultrasound exam: A procedure in which high-energy sound waves (ultrasound) are bounced off internal tissues or organs, such as the bladder, and make echoes. The echoes form a picture of body tissues called a sonogram. The picture can be printed to be looked at later.

Talk to your child's doctor about whether your child needs to have tests and procedures to check for signs of bladder late effects. If tests are needed, find out how often they should be done.

To Learn More About Late Effects of Treatment for Childhood Cancer

For more information about late effects of treatment for childhood cancer, see the following:

• Long-Term Follow-Up Guidelines for Survivors of Childhood, Adolescent, and Young Adult Cancers
• Late Effects Directory of Services
• Computed Tomography (CT) Scans and Cancer

For more childhood cancer information and other general cancer resources from the National Cancer Institute, see the following:

• Childhood Cancers
• CureSearch for Children's Cancer
• Adolescents and Young Adults with Cancer
• Children with Cancer: A Guide for Parents
• Cancer in Children and Adolescents
• Staging
• Coping with Cancer
• Questions to Ask Your Doctor About Cancer
• For Survivors and Caregivers

About This PDQ Summary

About PDQ

Physician Data Query (PDQ) is the National Cancer Institute's (NCI's) comprehensive cancer information database. The PDQ database contains summaries of the latest published information on cancer prevention, detection, genetics, treatment, supportive care, and complementary and alternative medicine. Most summaries come in two versions. The health professional versions have detailed information written in technical language. The patient versions are written in easy-to-understand, nontechnical language. Both versions have cancer information that is accurate and up to date and most versions are also available in Spanish.

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Purpose of This Summary

This PDQ cancer information summary has current information about the late effects of treatment for childhood cancer. It is meant to inform and help patients, families, and caregivers. It does not give formal guidelines or recommendations for making decisions about health care.

Reviewers and Updates

Editorial Boards write the PDQ cancer information summaries and keep them up to date. These Boards are made up of experts in cancer treatment and other specialties related to cancer. The summaries are reviewed regularly and changes are made when there is new information. The date on each summary ("Updated") is the date of the most recent change.

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A clinical trial is a study to answer a scientific question, such as whether one treatment is better than another. Trials are based on past studies and what has been learned in the laboratory. Each trial answers certain scientific questions in order to find new and better ways to help cancer patients. During treatment clinical trials, information is collected about the effects of a new treatment and how well it works. If a clinical trial shows that a new treatment is better than one currently being used, the new treatment may become "standard." Patients may want to think about taking part in a clinical trial. Some clinical trials are open only to patients who have not started treatment.

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The best way to cite this PDQ summary is:

PDQ® Pediatric Treatment Editorial Board. PDQ Late Effects of Treatment for Childhood Cancer. Bethesda, MD: National Cancer Institute. Updated <MM/DD/YYYY>. Available at: https://www.cancer.gov/types/childhood-cancers/late-effects-pdq. Accessed <MM/DD/YYYY>. [PMID: 26389365]

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Last Revised: 2022-10-13

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