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Cancer in Children and Adolescents

How common is cancer in children and adolescents?

Although cancer in children and adolescents is rare, it is the leading cause of death by disease after infancy among children in the United States (1). It is estimated that, in 2023, a total of 15,190 children and adolescents ages 0 to 19 will be diagnosed with cancer and 1,590 will die of the disease in the United States (2). Among children (ages 0 to 14 years), it is estimated that 9910 will be diagnosed with cancer and 1040 will die of the disease (2). And among adolescents (ages 15 to 19 years), it is estimated that 5280 will be diagnosed with cancer and 550 will die of the disease (2).

In the United States, the most common types of cancer diagnosed in 2016–2020 among children and adolescents were leukemias, malignant  brain and other central nervous system (CNS) tumors, lymphomas, malignant soft tissue sarcomas, malignant germ cell tumors, and malignant bone tumors. 

The most common types of cancer among children and adolescents differed by age group. For example, leukemias were more common in those ages 1 to 4 than in other age groups and lymphomas were more common in those ages 15 to 19 than in other age groups.

Rates of the most common types of childhood and adolescent cancer also differ by race/ethnicity. For example, in 2016–2020, the incidence rate of leukemia was about twice as high in Hispanic and American Indian/Alaska Native children and adolescents as in Black children and adolescents. During the same time period, the rates of brain and other nervous system tumors were higher in White and American Indian/Alaska Native children and adolescents than in those of all other racial and ethnic groups.

As of January 1, 2020 (the most recent date for which data exist), approximately 495,739 survivors of childhood and adolescent cancer (diagnosed at ages 0 to 19 years) were estimated to be alive in the United States. The number of survivors will continue to increase, given that the incidence of cancer in children and adolescents has been rising slightly in recent decades and that survival rates overall are improving.

What is the prognosis for children and adolescents with cancer?  

The overall outlook for children and adolescents with cancer has improved greatly over the last half-century. In the mid-1970s, 58% of children (ages 0 to 14 years) and 68% of adolescents (ages 15 to 19 years) diagnosed with cancer survived at least 5 years (3). In 2013–2019, 5-year survival was 83.2% for children younger than 1 year, 87.8% for children ages 1–4 years, 85.7% for children ages 5–9 years, 85.5% for children ages 10–14 years, and 87.3% for adolescents ages 15–19 years.

Although the 5-year survival rates—the percentage still alive 5 years after diagnosis—for most childhood cancers have improved in recent decades, the improvement has been especially dramatic for a few cancers, particularly acute lymphoblastic leukemia (ALL), the most common childhood cancer. Improved treatments for ALL introduced beginning in the 1960s and 1970s raised the 5-year survival rate for children diagnosed with this disease from 57% in 1975 to 92.1% in 2013–2019. The 5-year survival rate for children diagnosed with non-Hodgkin lymphoma also increased dramatically, from 43% in 1975 to 91.4% in 2013–2019.

In contrast, survival rates remain poor for some cancer types, for some age groups, and for some cancers within a site. For example:

Adolescents and young adults with ALL may have better outcomes if they are treated with pediatric treatment regimens than if they receive adult treatment regimens (6, 7). Possibly as a result of the increased use of these regimens, survival of adolescents and young adults with ALL has improved in recent years, even though their survival is still poorer than that of younger children with the disease (8).

The cancer mortality rate—the number of deaths due to cancer per 100,000 people per year—among children and adolescents younger than 20 years declined by more than 50% from 1975 to 2020. Specifically, the mortality rate was 5.1 per 100,000 children and adolescents in 1975 and 2.1 per 100,000 children and adolescents in 2020. 

However, despite the overall decrease in mortality, approximately 1,600 children and adolescents still die of cancer each year in the United States, indicating that new advances and continued research to identify effective treatments are required to further reduce childhood cancer mortality.

What are the possible causes of cancer in children and adolescents?

Most cancers in children, like those in adults, have alterations (changes, or mutations) in genes that lead to uncontrolled cell growth and eventually cancer. Genetic changes (or variants) that are passed from parents to their children—known as germline variants—can be associated with an increased risk of cancer. Genetic changes that lead to cancer can also occur spontaneously in cells during development.

Inherited genetic changes

About 8% to 10% of all cancers in children overall are caused by an inherited pathogenic variant (harmful alteration) in a cancer predisposition gene, although the percentage varies across cancer types (911). For example, about 45% of children with retinoblastoma, a cancer of the eye that develops mainly in children, inherited a pathogenic variant in a gene called RB1 from a parent (12). Children who inherit variants associated with certain familial syndromes, such as Li-Fraumeni syndrome, Beckwith-Wiedemann syndrome, Fanconi anemia, Noonan syndrome, and von Hippel-Lindau syndrome, also have an increased risk of childhood cancer.

Genetic changes early in development

Rare genetic changes that arise during development of one of the germ cells (sperm or egg) that unite to form the zygote that becomes a child can increase the risk of cancer in that child. Genetic changes can include broken, missing, rearranged, or extra chromosomes as well as gene variants. One such alteration is trisomy 21, or the presence of an extra copy of chromosome 21, which causes Down syndrome. Children with Down syndrome are 10–20 times more likely to develop leukemia than children without Down syndrome (13). However, only a very small proportion of childhood leukemia is linked to Down syndrome.

Environmental exposures

Genetic changes that may cause cancer can also occur in different cells of the body after birth, as the body is actively growing and developing during early childhood (14). The extent to which these changes reflect environmental exposures is unclear. Certain substances in the environment, such as cigarette smoke, asbestos, and ultraviolet (UV) radiation from the sun, are known to cause genetic changes that can lead to cancer. However, environmental causes of childhood cancer have been particularly difficult to identify, partly because cancer in children is rare and partly because it is difficult to determine what children might have been exposed to early in their development. 

Nevertheless, several environmental exposures have been linked to childhood or adolescent cancer. For example, one study found that melanoma in children and adolescents (ages 11–20 years) has many genomic similarities to melanoma that occurs in adults, including an enrichment of UV-induced mutations (15). And ionizing radiation can lead to the development of leukemia and other cancers in children and adolescents. Children and adolescents who were exposed to radiation from the atomic bombs dropped in Japan during the Second World War had an elevated risk of leukemia (16), and children who were exposed to radiation from the Chernobyl nuclear plant accident had an elevated risk for thyroid cancer (17). 

Exposure of parents to ionizing radiation is also a possible concern in terms of the development of cancer in their future offspring. Children whose mothers had x-rays during pregnancy (that is, children who were exposed before birth) or who were exposed after birth to diagnostic medical radiation from computed tomography (CT) scans have been found to have a slight increase in risk of leukemia and brain tumors, and possibly other cancers (18). However, genomic analysis of children born to people exposed to radiation at Chernobyl indicates that this exposure did not lead to an increase in new genetic changes being passed from parent to child (19).

Several other environmental exposures of parents have also been associated with childhood cancer. For some types of childhood leukemia (particularly acute lymphoblastic leukemia), associations have been described for father’s tobacco smoking (20, 21) and for parental exposure to certain pesticides at their workplace (2224). Studies of childhood brain tumors have suggested associations with maternal consumption of cured meats (25).

Factors associated with reduced risks of childhood cancer

Researchers have also identified factors that may be associated with reduced risk of childhood cancer. For example, maternal consumption of folate has been associated with reduced risks of both leukemia and brain tumors in children (26). Being breastfed and having been exposed to routine childhood infections are both associated with a lower risk of developing childhood leukemia (27).

What does a child’s cancer diagnosis mean for cancer risk in the rest of the family?

First- and second-degree relatives of a child diagnosed with cancer may be at increased risk for developing cancer if there is already a family history of cancer—that is, if the child’s cancer is likely due to an inherited genetic disorder (28). A clinician may advise as to whether a child and family members could benefit from genetic testing or referral to a medical geneticist or cancer genetic counselor for evaluation (2830).

How do cancers in adolescents and young adults differ from those in younger children?

Cancer occurs more frequently in adolescents and young adults ages 15 to 39 years than in younger children, although incidence in this group is still much lower than in older adults. According to the NCI Surveillance, Epidemiology, and End Results (SEER) Program, each year in 2016–2020 there were:

  • 17.4 cancer diagnoses per 100,000 children ages younger than 15 years
  • 75.3 cancer diagnoses per 100,000 adolescents and young adults ages 15 to 39 years
  • 534.4 cancer diagnoses per 100,000 adults ages 40 to 64 years

The most frequent cancers diagnosed in adolescents and young adults (AYAs) are cancers that are more common among adults than younger children, such as breast cancer, melanoma, and thyroid cancer (31). But certain cancers, such as testicular cancer, are more likely to be diagnosed among AYAs than among either younger children or adults. However, the incidence of specific cancer types varies widely across the adolescent and young adult age continuum.

Where do children and adolescents with cancer get treated?

Children and adolescents who have cancer are often treated at a children’s cancer center, which is a hospital or a unit within a hospital that specializes in diagnosing and treating patients through 20 years of age. The health professionals at these centers have specific training and expertise to provide comprehensive care for children and adolescents with cancer, and their families.

Children’s cancer centers also participate in clinical trials. The improvements in survival for children with cancer that have occurred over the past half century have been achieved because of treatment advances that were studied and proven to be effective in clinical trials.

More than 90% of children and adolescents who are diagnosed with cancer each year in the United States are cared for at a children’s cancer center that is affiliated with the NCI-supported Children’s Oncology Group (COG). COG is the world’s largest organization that performs clinical research to improve the care and treatment of children and adolescents with cancer. Each year, approximately 4,000 children who are diagnosed with cancer enroll in a COG-sponsored clinical trial. COG trials are sometimes open to older individuals when the type of cancer being studied is one that occurs in children, adolescents, and young adults.

Children’s cancer centers that participate in COG must meet and maintain strict standards of excellence for childhood cancer care. A directory of COG locations is available on their website. Families can ask their pediatrician or family doctor for a referral to a children’s cancer center. Families and health professionals can call NCI's Cancer Information Service at 1-800-4-CANCER (1-800-422-6237) to learn more about children’s cancer centers that belong to COG.

If my child is treated at a children’s cancer center, will they automatically be part of a clinical trial?

No. Participation in a clinical trial is voluntary, and it is up to each family in collaboration with their treatment team to decide if clinical trial participation is right for their child.

Can children and adolescents who have cancer be treated at the National Institutes of Health (NIH) Clinical Center?

Children and adolescents with cancer may be eligible to be treated in clinical trials at the NIH Clinical Center in Bethesda, Maryland. Because the NIH Clinical Center is a research hospital, only patients who have a specific type or stage of cancer that is under study can be accepted for treatment. In some cases, patients with conditions that are rare or difficult to diagnose may also be accepted for treatment at the NIH Clinical Center. All patients who are treated at the NIH Clinical Center must be referred by a physician.  

NCI’s Pediatric Oncology Branch conducts clinical trials at the NIH Clinical Center for children, adolescents, and young adults with a wide variety of cancers. Patients with newly diagnosed cancer, as well as patients whose cancers have come back after treatment, may be eligible to participate in a clinical trial. Physicians at the Pediatric Oncology Branch can also provide a second opinion on a patient’s diagnosis or treatment plan. To refer a patient to the Pediatric Oncology Branch, the patient’s health care provider should call 240-760-6403 (local) or 1-833-248-0479 (toll-free) weekdays between 8:30 a.m. and 5:00 p.m. ET. Parents can also call these numbers to learn if their child is eligible to participate in a clinical trial.

NCI’s Clinical Genetics Branch conducts long-term observational and clinical studies of genetic susceptibility to cancer, mostly in families with a known or suspected cancer predisposition syndrome, or families that have a higher-than-expected rate of cancer. Although some of these study participants, including children and adolescents, are seen at the NIH Clinical Center, the genetic susceptibility studies do not evaluate treatment or other interventions, as in a clinical trial. Information about active studies that enroll children and adolescents can be obtained by contacting the referral nurse at 1-800-518-8474.

What should survivors of childhood and adolescent cancer consider after they complete treatment?

Some people who have had cancer during childhood or adolescence may need follow-up care and enhanced medical surveillance as they get continue to get older because of the risk of complications related to the disease or its treatment that can last for, or arise, many years after they complete treatment for their cancer (32, 33). Health problems that develop months or years after treatment has ended are known as late effects.

The specific late effects that a person who was treated for childhood cancer might experience depend on the type and location of their cancer, the type of treatment they received, and patient-related factors, such as age at diagnosis. Additionally, some people with a history of childhood cancer may need additional follow-up if an inherited genetic alteration is found to be the cause of the cancer.

Children and adolescents who were treated for bone cancer, brain tumors, or Hodgkin lymphoma, or who received radiation to their chest, abdomen, or pelvis, have the highest risk of serious late effects from their cancer treatment, including second cancers, joint replacement, hearing loss, and congestive heart failure (3436).

Long-term follow-up analysis of a cohort of survivors of childhood cancer treated between 1970 and 1986 has shown that these survivors remain at risk of complications and premature death as they age, with more than half of them having experienced a severe or disabling complication or even death by the time they reach age 50 years (37). Children and adolescents treated in more recent decades may have lower risks of late effects due to modifications in treatment regimens to reduce exposure to radiotherapy and chemotherapy, increased efforts to detect late effects, and improvements in medical care for late effects (36, 38, 39).

It’s important for people who had cancer during childhood or adolescence to have regular medical follow-up examinations so any health problems can be identified and treated as soon as possible. The Children’s Oncology Group (COG) has developed long-term follow-up guidelines for survivors of childhood, adolescent, and young adult cancers.

It is also important to keep a record of the details of the cancer diagnosis and the treatment that was received. This record should include:

  • the type and stage of cancer
  • date of cancer diagnosis and dates of any relapses
  • genetic testing for inherited variants and somatic (tumor) variants
  • types and dates of imaging tests
  • contact information for the hospitals and doctors who provided treatment
  • names and total doses of all chemotherapy drugs used in treatment
  • the parts of the body that were treated with radiation and the total doses of radiation that were given
  • types and dates of all surgeries
  • any other cancer treatments received
  • any serious complications that occurred during treatment and how those complications were treated
  • the date that cancer treatment was completed

The record should be kept in a safe place, and copies of the record should be given to all doctors or other health care providers who are involved with the child’s follow-up care, even as the child grows into adulthood.

Many cancer centers have programs to help patients and families navigate long-term survivor care, including both the physical and emotional issues they may face after treatment. Many children’s cancer centers have clinics where survivors of childhood cancer can go for follow-up care until they reach their early 20s. Some cancer centers are now creating clinics dedicated to follow-up care for long-term cancer survivors of pediatric and adolescent cancers. Programs focused on adolescent and young adult (AYA) cancer survivors address some of the more unique needs of these patients, including discussing and preserving future fertility, peer support, and psychosocial support that addresses personal issues such as finances, education, occupational impacts, and transition to independence.

Selected References
  1. Siegel DA, King JB, Lupo PJ, et al. Counts, incidence rates, and trends of pediatric cancer in the United States, 2003–2019. Journal of the National Cancer Institute 2023: djad115. doi: 10.1093/jnci/djad115.

    [PubMed Abstract]
  2. Siegel RL, Miller KD, Wagle NS, Jemal A. Cancer statistics, 2023. CA: A Cancer Journal for Clinicians 2023; 73(1):17–48. doi: 10.3322/caac.21763.

    [PubMed Abstract]
  3. Siegel RL, Miller KD, Fuchs HE, Jemal A. Cancer Statistics, 2021. CA: A Cancer Journal for Clinicians 2021; 71(1):7–33. doi: 10.3322/caac.21654. Erratum in: CA Cancer J Clin. 2021 Jul;71(4):359.

    [PubMed Abstract]
  4. Hargrave D, Bartels U, Bouffet E. Diffuse brainstem glioma in children: Critical review of clinical trials. Lancet Oncology 2006; 7(3):241–248. doi: 10.1016/S1470-2045(06)70615-5.

    [PubMed Abstract]
  5. American Cancer Society. Cancer Facts & Figures 2023. Atlanta: American Cancer Society; 2023.

  6. Ram R, Wolach O, Vidal L, et al. Adolescents and young adults with acute lymphoblastic leukemia have a better outcome when treated with pediatric-inspired regimens: Systematic review and meta-analysis. American Journal of Hematology 2012; 87(5):472–478.

    [PubMed Abstract]
  7. Stock W, Luger SM, Advani AS, et al. A pediatric regimen for older adolescents and young adults with acute lymphoblastic leukemia: Results of CALGB 10403. Blood 2019; 133(14):1548–1559. doi: 10.1182/blood-2018-10-881961. Epub 2019 Jan 18. Erratum in: Blood. 2019 Sep 26;134(13):1111.

    [PubMed Abstract]
  8. Björkholm M, Edgren G, Dickman PW. Trends in survival of young adult patients with acute lymphoblastic leukemia in Sweden and the United States. Blood 2019; 134(4):407–410. doi: 10.1182/blood.2019001168.

    [PubMed Abstract]
  9. Gröbner SN, Worst BC, Weischenfeldt J, et al. The landscape of genomic alterations across childhood cancers. Nature 2018; 555(7696):321–327.

    [PubMed Abstract]
  10. Zhang J, Walsh MF, Wu G, et al. Germline mutations in predisposition genes in pediatric cancer. New England Journal of Medicine 2015; 373:2336–2346.

    [PubMed Abstract]
  11. Bakhuizen JJ, Hopman SMJ, Bosscha MI, et al. Assessment of cancer predisposition syndromes in a national cohort of children with a neoplasm. JAMA Network Open 2023; 6(2):e2254157. doi: 10.1001/jamanetworkopen.2022.54157.

    [PubMed Abstract]
  12. Dimaras H, Corson TW, Cobrinik D, et al. Retinoblastoma. Nature Reviews. Disease Primers. 2015; 1:15021.

    [PubMed Abstract]
  13. Ross JA, Spector LG, Robison LL, Olshan AF. Epidemiology of leukemia in children with Down syndrome. Pediatric Blood and Cancer 2005; 44(1):8–12.

    [PubMed Abstract]
  14. Moore L, Cagan A, Coorens THH, et al. The mutational landscape of human somatic and germline cells. Nature 2021; 597(7876):381–386.

    [PubMed Abstract]
  15. Lu C, Zhang J, Nagahawatte P, et al. The genomic landscape of childhood and adolescent melanoma. Journal of Investigative Dermatology 2015; 135(3):816–823.

    [PubMed Abstract]
  16. Hsu WL, Preston DL, Soda M, et al. The incidence of leukemia, lymphoma and multiple myeloma among atomic bomb survivors: 1950–2001. Radiation Research 2013; 179(3):361–382.

    [PubMed Abstract]
  17. Cardis E, Hatch M. The Chernobyl accident--an epidemiological perspective. Clinical Oncology: A Journal of the Royal College of Radiologists 2011; 23(4):251–260.

    [PubMed Abstract]
  18. Pearce MS, Salotti JA, Little MP, et al. Radiation exposure from CT scans in childhood and subsequent risk of leukaemia and brain tumours: A retrospective cohort study. Lancet 2012; 380(9840):499–505.

    [PubMed Abstract]
  19. Yeager M, Machiela MJ, Kothiyal P, et al. Lack of transgenerational effects of ionizing radiation exposure from the Chernobyl accident. Science 2021; 372(6543):725–729.

    [PubMed Abstract]
  20. Liu R, Zhang L, McHale CM, Hammond SK. Paternal smoking and risk of childhood acute lymphoblastic leukemia: Systematic review and meta-analysis. Journal of Oncology 2011; 2011:854584.

    [PubMed Abstract]
  21. Cao Y, Lu J, Lu J. Paternal smoking before conception and during pregnancy is associated with an increased risk of childhood acute lymphoblastic leukemia: A systematic review and meta-analysis of 17 case–control studies. Journal of Pediatric Hematology/Oncology 2020; 42(1):32–40.

    [PubMed Abstract]
  22. Van Maele-Fabry G, Lantin AC, Hoet P, Lison D. Childhood leukaemia and parental occupational exposure to pesticides: A systematic review and meta-analysis. Cancer Causes & Control 2010; 21(6):787–809.

    [PubMed Abstract]
  23. Vinson F, Merhi M, Baldi I, Raynal H, Gamet-Payrastre L. Exposure to pesticides and risk of childhood cancer: A meta-analysis of recent epidemiological studies. Occupational and Environmental Medicine 2011; 68(9):694–702.

    [PubMed Abstract]
  24. Karalexi MA, Tagkas CF, Markozannes G, et al. Exposure to pesticides and childhood leukemia risk: A systematic review and meta-analysis. Environmental Pollution 2021; 285:117376.

    [PubMed Abstract]
  25. Johnson KJ, Cullen J, Barnholtz-Sloan JS, et al. Childhood brain tumor epidemiology: A brain tumor epidemiology consortium review. Cancer Epidemiology, Biomarkers & Prevention 2014; 23(12):2716–2736.

    [PubMed Abstract]
  26. Chiavarini M, Naldini G, Fabiani R. Maternal folate intake and risk of childhood brain and spinal cord tumors: A systematic review and meta-analysis. Neuroepidemiology 2018; 51(1–2):82–95.

    [PubMed Abstract]
  27. Amitay EL, Keinan-Boker L. Breastfeeding and childhood leukemia incidence: A meta-analysis and systematic review. JAMA Pediatrics 2015; 169(6):e151025.

    [PubMed Abstract]
  28. Curtin K, Smith KR, Fraser A, et al. Familial risk of childhood cancer and tumors in the Li-Fraumeni spectrum in the Utah Population Database: Implications for genetic evaluation in pediatric practice. International Journal of Cancer 2013; 133(10):2444–2453.

    [PubMed Abstract]
  29. Malkin D, Nichols KE, Schiffman JD, Plon SE, Brodeur GM. The future of surveillance in the context of cancer predisposition: Through the murky looking glass. Clinical Cancer Research 2017; 23(21):e133–e137.

    [PubMed Abstract]
  30. Schiffman JD. Hereditary cancer syndromes: if you look, you will find them. Pediatric Blood & Cancer 2012; 58(1):5–6. DOI: 10.1002/pbc.23336

  31. Barr RD, Ries LA, Lewis DR, et al. Incidence and incidence trends of the most frequent cancers in adolescent and young adult Americans, including "nonmalignant/noninvasive" tumors. Cancer 2016; 122(7):1000–1008.

    [PubMed Abstract]
  32. Robison LL, Hudson MM. Survivors of childhood and adolescent cancer: Life-long risks and responsibilities. Nature Reviews Cancer 2014; 14(1):61–70.

    [PubMed Abstract]
  33. Bhatia S, Tonorezos ES, Landier W. Clinical care for people who survive childhood cancer: A review. JAMA 2023; 330(12):1175–1186.

    [PubMed Abstract]
  34. Oeffinger KC, Mertens AC, Sklar CA, et al. Chronic health conditions in adult survivors of childhood cancer. New England Journal of Medicine 2006; 355(15):1572–1582.

    [PubMed Abstract]
  35. Meadows AT, Friedman DL, Neglia JP, et al. Second neoplasms in survivors of childhood cancer: Findings from the Childhood Cancer Survivor Study cohort. Journal of Clinical Oncology 2009; 27(14):2356–2362.

    [PubMed Abstract]
  36. Gibson TM, Mostoufi-Moab S, Stratton KL, et al. Temporal patterns in the risk of chronic health conditions in survivors of childhood cancer diagnosed 1970–99: A report from the Childhood Cancer Survivor Study cohort. Lancet Oncology 2018; 19(12):1590–1601.

    [PubMed Abstract]
  37. Armstrong GT, Kawashima T, Leisenring W, et al. Aging and risk of severe, disabling, life-threatening, and fatal events in the Childhood Cancer Survivor Study. Journal of Clinical Oncology 2014; 32(12):1218–1227.

    [PubMed Abstract]
  38. Turcotte LM, Liu Q, Yasui Y, et al. Temporal trends in treatment and subsequent neoplasm risk among 5-year survivors of childhood cancer, 1970–2015. JAMA 2017; 317(8):814–824.

    [PubMed Abstract]
  39. Armstrong GT, Chen Y, Yasui Y, et al. Reduction in late mortality among 5-year survivors of childhood cancer. New England Journal of Medicine 2016; 374(9):833–842.

    [PubMed Abstract]
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