Skip to main content

Specific Issues of Children and Young Adults in Survivorship Care

  • Chapter
  • First Online:
Survivorship Care for Cancer Patients

Abstract

Therapeutic advances in pediatric oncology have made it possible to increase 5-year survival rates for all types of cancer to 80%, allowing a growing number of children to be cured and reach adulthood. Currently, in the European Union, approximately 50,000 new cases of cancer are diagnosed each year in people under 25 years of age. Nevertheless, cancer remains the main cause of disease-related mortality in children, justifying aggressive treatment. This increase in survival rate is not without cost to the cured child/young adult. Several publications have described cumulative prevalence rates between 40–84% of long-term sequelae due to their cancer and its treatment, which can be disabling and/or life-threatening. Mortality increases significantly over time: 6.5% at 10 years (95% confidence interval [CI], 6.2–6.9), 11.9% at 20 years (95% CI, 11.5–12.4), and then 18.1% at 30 years (95% CI, 17.3–18.9). Premature mortality is essentially due to recurrence of original cancer (>50%), and particularly in the early years, subsequent neoplasm (10–20%) and cardiovascular diseases (5–10%). The most common complication is endocrine disorder and affects 40–60% of childhood cancer survivors, although less among young adult cancer survivors. Compared to childhood cancer survivors, adolescent and young adult survivors had a lower risk of death from causes related to the late effects of cancer therapy 4.8 (95% CI, 4.4–5.1) versus 6.8 (95% CI, 6.2–7.4), respectively. Abundant researches describe long-term adverse outcomes involving physical health, including growth and development, organ function, reproductive capacity, and risk of subsequent carcinogenesis, but also metabolic dysfunction, psychological issues, and neurocognitive deficits. Several studies suggest that 20–30% of survivors report moderate to severe psychological distress. Cancer survivors treated in childhood are almost twice as likely to be unemployed as the control population; this excess risk is only significant for those who had central nervous system tumors.

In conclusion, it is highly recommended that survivors attend personalized, long-term follow-up care that should ideally be performed using a global and comprehensive approach. This follow-up approach should also be interdisciplinary and focus on preventing or managing late effects through screening, education (of survivors and general practitioners) on treatment-related complications, and should encourage preventative lifestyle behaviors.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Subscribe and save

Springer+ Basic
$34.99 /Month
  • Get 10 units per month
  • Download Article/Chapter or eBook
  • 1 Unit = 1 Article or 1 Chapter
  • Cancel anytime
Subscribe now

Buy Now

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 89.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 119.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 169.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Similar content being viewed by others

References

  1. Jemal A, et al. Cancer statistics, 2010. CA Cancer J Clin. 2010;60(5):277–300.

    Article  PubMed  Google Scholar 

  2. Miller KD, et al. Cancer statistics for adolescents and young adults, 2020. CA Cancer J Clin. 2020;70(6):443–59.

    Article  PubMed  Google Scholar 

  3. Brenner H, Gondos A, Pulte D. Ongoing improvement in long-term survival of patients with Hodgkin disease at all ages and recent catch-up of older patients. Blood. 2008;111(6):2977–83.

    Article  CAS  PubMed  Google Scholar 

  4. Lacour B, et al. Childhood cancer survival in France, 2000-2008. Eur J Cancer Prev. 2014;23(5):449–57.

    Article  PubMed  Google Scholar 

  5. Berger C, et al. [Childhood cancer incidence and survival rates in the Rhone-Alpes regional paediatric registry 1987–1999]. Arch Pediatr. 2006;13(2):121–129.

    Google Scholar 

  6. Norsker FN, et al. Late effects in childhood cancer survivors: early studies, survivor cohorts, and significant contributions to the field of late effects. Pediatr Clin N Am. 2020;67(6):1033–49.

    Article  Google Scholar 

  7. Steliarova-Foucher E, et al. Geographical patterns and time trends of cancer incidence and survival among children and adolescents in Europe since the 1970s (the ACCISproject): an epidemiological study. Lancet. 2004;364(9451):2097–105.

    Article  PubMed  Google Scholar 

  8. Gatta G, et al. Childhood cancer survival in Europe 1999-2007: results of EUROCARE-5—a population-based study. Lancet Oncol. 2014;15(1):35–47.

    Article  PubMed  Google Scholar 

  9. Pritchard-Jones K, Hargrave D. Declining childhood and adolescent cancer mortality: great progress but still much to be done. Cancer. 2014;120(16):2388–91.

    Article  PubMed  Google Scholar 

  10. O’Leary M, et al. Progress in childhood cancer: 50 years of research collaboration, a report from the Children’s Oncology Group. Semin Oncol. 2008;35(5):484–93.

    Article  PubMed  PubMed Central  Google Scholar 

  11. Garolla A, et al. Progress in the development of childhood cancer therapy. Reprod Toxicol. 2006;22(2):126–32.

    Article  CAS  PubMed  Google Scholar 

  12. Smith M, Hare ML. An overview of progress in childhood cancer survival. J Pediatr Oncol Nurs. 2004;21(3):160–4.

    Article  PubMed  Google Scholar 

  13. Bleyer A. Latest estimates of survival rates of the 24 most common cancers in adolescent and young adult Americans. J Adolesc Young Adult Oncol. 2011;1(1):37–42.

    Article  PubMed  Google Scholar 

  14. Robison LL, Hudson MM. Survivors of childhood and adolescent cancer: life-long risks and responsibilities. Nat Rev Cancer. 2014;14(1):61–70.

    Article  CAS  PubMed  Google Scholar 

  15. Demoor-Goldschmidt C, et al. Long-term follow-up after childhood cancer in France supported by the SFCE-force and weakness-current state, results of a questionnaire and perspectives. Br J Radiol. 2018;91(1084):20170819.

    Article  PubMed  PubMed Central  Google Scholar 

  16. Oeffinger KC, Hudson MM. Long-term complications following childhood and adolescent cancer: foundations for providing risk-based health care for survivors. CA Cancer J Clin. 2004;54(4):208–36.

    Article  PubMed  Google Scholar 

  17. Suh E, et al. Late mortality and chronic health conditions in long-term survivors of early-adolescent and young adult cancers: a retrospective cohort analysis from the Childhood Cancer Survivor Study. Lancet Oncol. 2020;21(3):421–35.

    Article  PubMed  PubMed Central  Google Scholar 

  18. Fidler-Benaoudia MM, et al. A comparison of late mortality among survivors of childhood cancer in the United States and United Kingdom. J Natl Cancer Inst. 2021;113(5):562–71.

    Article  PubMed  Google Scholar 

  19. Fidler MM, et al. Long term cause specific mortality among 34 489 five year survivors of childhood cancer in Great Britain: population based cohort study. BMJ. 2016;354:i4351.

    Article  PubMed  PubMed Central  Google Scholar 

  20. Dama E, et al. Late deaths among five-year survivors of childhood cancer. A population-based study in Piedmont Region, Italy. Haematologica. 2006;91(8):1084–91.

    PubMed  Google Scholar 

  21. Armstrong GT, et al. Aging and risk of severe, disabling, life-threatening, and fatal events in the Childhood Cancer Survivor Study. J Clin Oncol. 2014;32(12):1218–27.

    Article  PubMed  PubMed Central  Google Scholar 

  22. Mertens AC. Cause of mortality in 5-year survivors of childhood cancer. Pediatr Blood Cancer. 2007;48(7):723–6.

    Article  PubMed  Google Scholar 

  23. Mertens AC, et al. Cause-specific late mortality among 5-year survivors of childhood cancer: the Childhood Cancer Survivor Study. J Natl Cancer Inst. 2008;100(19):1368–79.

    Article  PubMed  PubMed Central  Google Scholar 

  24. Gibson TM, Robison LL. Impact of cancer therapy-related exposures on late mortality in childhood cancer survivors. Chem Res Toxicol. 2015;28(1):31–7.

    Article  CAS  PubMed  Google Scholar 

  25. Moskowitz CS, et al. Breast cancer after chest radiation therapy for childhood cancer. J Clin Oncol. 2014;32(21):2217–23.

    Article  PubMed  PubMed Central  Google Scholar 

  26. Reulen, RC, et al., Risk of digestive cancers in a cohort of 69 460 five-year survivors of childhood cancer in Europe: the PanCareSurFup study. Gut. 2020.

    Google Scholar 

  27. Reulen RC, et al. Long-term risks of subsequent primary neoplasms among survivors of childhood cancer. JAMA. 2011;305(22):2311–9.

    Article  CAS  PubMed  Google Scholar 

  28. Dietz AC, et al. Solid organ transplantation after treatment for childhood cancer: a retrospective cohort analysis from the Childhood Cancer Survivor Study. Lancet Oncol. 2019;20(10):1420–31.

    Article  PubMed  PubMed Central  Google Scholar 

  29. Khanna A, et al. Increased risk of all cardiovascular disease subtypes among childhood cancer survivors: population-based matched cohort study. Circulation. 2019;140(12):1041–3.

    Article  PubMed  Google Scholar 

  30. Haddy N, et al. Cardiac diseases following childhood cancer treatment: cohort study. Circulation. 2016;133(1):31–8.

    Article  CAS  PubMed  Google Scholar 

  31. Barlogis V, et al. Late cardiomyopathy in childhood acute myeloid leukemia survivors: a study from the L.E.A. program. Haematologica. 2015;100(5):e186–9.

    Article  PubMed  PubMed Central  Google Scholar 

  32. Bates JE, et al. Therapy-related cardiac risk in childhood cancer survivors: an analysis of the Childhood Cancer Survivor Study. J Clin Oncol. 2019;37(13):1090–101.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  33. van der Pal HJ, et al. Cardiac function in 5-year survivors of childhood cancer: a long-term follow-up study. Arch Intern Med. 2010;170(14):1247–55.

    PubMed  Google Scholar 

  34. van der Pal HJ, et al. High risk of symptomatic cardiac events in childhood cancer survivors. J Clin Oncol. 2012;30(13):1429–37.

    Article  PubMed  Google Scholar 

  35. van der Pal HJ, et al. Valvular abnormalities detected by echocardiography in 5-year survivors of childhood cancer: a long-term follow-up study. Int J Radiat Oncol Biol Phys. 2015;91(1):213–22.

    Article  PubMed  Google Scholar 

  36. Henson KE, et al. Cardiac mortality after radiotherapy, chemotherapy and endocrine therapy for breast cancer: cohort study of 2 million women from 57 cancer registries in 22 countries. Int J Cancer. 2020;147(5):1437–49.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  37. Henson KE, et al. Radiation-related mortality from heart disease and lung cancer more than 20 years after radiotherapy for breast cancer. Br J Cancer. 2013;108(1):179–82.

    Article  CAS  PubMed  Google Scholar 

  38. Henson KE, et al. Cardiac mortality among 200 000 five-year survivors of cancer diagnosed at 15 to 39 years of age: the teenage and young adult cancer survivor study. Circulation. 2016;134(20):1519–31.

    Article  PubMed  PubMed Central  Google Scholar 

  39. Bhakta N, et al. Cumulative burden of cardiovascular morbidity in paediatric, adolescent, and young adult survivors of Hodgkin’s lymphoma: an analysis from the St Jude Lifetime Cohort Study. Lancet Oncol. 2016;17(9):1325–34.

    Article  PubMed  PubMed Central  Google Scholar 

  40. Feijen E, et al. Risk and temporal changes of heart failure among 5-year childhood cancer survivors: a DCOG-LATER study. J Am Heart Assoc. 2019;8(1):e009122.

    Article  PubMed  Google Scholar 

  41. Arem H, Loftfield E. Cancer epidemiology: a survey of modifiable risk factors for prevention and survivorship. Am J Lifestyle Med. 2018;12(3):200–10.

    Article  PubMed  Google Scholar 

  42. de Fine Licht S, et al. Risk factors for cardiovascular disease in 5-year survivors of adolescent and young adult cancer: a Danish population-based cohort study. Cancer. 2020;126(3):659–69.

    Article  PubMed  Google Scholar 

  43. Pein F, et al. [Cardiac toxicity of cancer treatment regimes in children and adolescents: physiopathology, clinical data and the paediatric oncologist’s point of view]. Bull Cancer. 2004;91(Suppl 3):185–91.

    Google Scholar 

  44. Bouillon K, et al. Long-term cardiovascular mortality after radiotherapy for breast cancer. J Am Coll Cardiol. 2011;57(4):445–52.

    Article  PubMed  Google Scholar 

  45. Feijen EA, et al. Late cardiac events after childhood cancer: methodological aspects of the Pan-European Study PanCareSurFup. PLoS One. 2016;11(9):e0162778.

    Article  PubMed  PubMed Central  CAS  Google Scholar 

  46. Feijen EAM, et al. Increased risk of cardiac ischaemia in a pan-European cohort of 36 205 childhood cancer survivors: a PanCareSurFup study. Heart. 2021;107(1):33–40.

    Article  PubMed  Google Scholar 

  47. Guldner L, et al. Radiation dose and long term risk of cardiac pathology following radiotherapy and anthracyclin for a childhood cancer. Radiother Oncol. 2006;81(1):47–56.

    Article  PubMed  Google Scholar 

  48. Mansouri I, et al. The role of irradiated heart and left ventricular volumes in heart failure occurrence after childhood cancer. Eur J Heart Fail. 2019;21(4):509–18.

    Article  CAS  PubMed  Google Scholar 

  49. Tukenova M, et al. Role of cancer treatment in long-term overall and cardiovascular mortality after childhood cancer. J Clin Oncol. 2010;28(8):1308–15.

    Article  PubMed  Google Scholar 

  50. Lipshultz SE. Exposure to anthracyclines during childhood causes cardiac injury. Semin Oncol. 2006;33(3 Suppl 8):S8–14.

    Article  CAS  PubMed  Google Scholar 

  51. Lipshultz SE, Cochran TR, Wilkinson JD. Screening for long-term cardiac status during cancer treatment. Circ Cardiovasc Imaging. 2012;5(5):555–8.

    Article  PubMed  Google Scholar 

  52. Chen BB, et al. Comparison of long-term outcomes and sequelae between children and adult nasopharyngeal carcinoma treated with intensity modulated radiation therapy. Int J Radiat Oncol Biol Phys. 2020;106(4):848–56.

    Article  PubMed  Google Scholar 

  53. Brignardello E, et al. Endocrine health conditions in adult survivors of childhood cancer: the need for specialized adult-focused follow-up clinics. Eur J Endocrinol. 2013;168(3):465–72.

    Article  CAS  PubMed  Google Scholar 

  54. Brignardello E, et al. Gonadal status in long-term male survivors of childhood cancer. J Cancer Res Clin Oncol. 2016;142(5):1127–32.

    Article  CAS  PubMed  Google Scholar 

  55. Thomas-Teinturier C, Salenave S. [Endocrine sequelae after treatment of pediatric cancer: from childhood to adulthood]. Bull Cancer. 2015;102(7–8):612–21.

    Google Scholar 

  56. Hudson MM, et al. Clinical ascertainment of health outcomes among adults treated for childhood cancer. JAMA. 2013;309(22):2371–81.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  57. Chemaitilly W, Cohen LE. DIAGNOSIS OF ENDOCRINE DISEASE: endocrine late-effects of childhood cancer and its treatments. Eur J Endocrinol. 2017;176(4):R183–203.

    Article  CAS  PubMed  Google Scholar 

  58. Chemaitilly W, et al. Endocrine late effects in childhood cancer survivors. J Clin Oncol. 2018;36(21):2153–9.

    Article  CAS  PubMed  Google Scholar 

  59. Chemaitilly W, et al. Premature ovarian insufficiency in childhood cancer survivors: a report from the st. Jude Lifetime Cohort. J Clin Endocrinol Metab. 2017;102(7):2242–50.

    Article  PubMed  PubMed Central  Google Scholar 

  60. Chemaitilly W, Meacham LR. Epidemiology. Endocrine disorders in adult survivors of childhood cancer. Nat Rev Endocrinol. 2014;10(6):320–1.

    Article  PubMed  Google Scholar 

  61. Chemaitilly W, Sklar CA. Childhood cancer treatments and associated endocrine late effects: a concise guide for the pediatric endocrinologist. Horm Res Paediatr. 2019;91(2):74–82.

    Article  CAS  PubMed  Google Scholar 

  62. Lehmann V, et al. Gonadal functioning and perceptions of infertility risk among adult survivors of childhood cancer: a report from the St Jude Lifetime Cohort Study. J Clin Oncol. 2019;37(11):893–902.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  63. Bedatsova L, Drake MT. The skeletal impact of cancer therapies. Br J Clin Pharmacol. 2019;85(6):1161–8.

    Article  PubMed  PubMed Central  Google Scholar 

  64. Chemaitilly W, Hudson MM. Update on endocrine and metabolic therapy-related late effects observed in survivors of childhood neoplasia. Curr Opin Endocrinol Diabetes Obes. 2014;21(1):71–6.

    Article  CAS  PubMed  Google Scholar 

  65. Plotnikoff GA. Interventional nutrition in cancer survivorship. A case study. Minn Med. 2010;93(10):53–8.

    PubMed  Google Scholar 

  66. Vijayvergia N, Denlinger CS. Lifestyle factors in cancer survivorship: where we are and where we are headed. J Pers Med. 2015;5(3):243–63.

    Article  PubMed  PubMed Central  Google Scholar 

  67. de Vathaire F, et al. Radiation dose to the pancreas and risk of diabetes mellitus in childhood cancer survivors: a retrospective cohort study. Lancet Oncol. 2012;13(10):1002–10.

    Article  PubMed  Google Scholar 

  68. Hawkins ML, et al. Endocrine and metabolic diseases among colorectal cancer survivors in a population-based cohort. J Natl Cancer Inst. 2020;112(1):78–86.

    Article  PubMed  Google Scholar 

  69. Lustberg MB, Reinbolt RE, Shapiro CL. Bone health in adult cancer survivorship. J Clin Oncol. 2012;30(30):3665–74.

    Article  CAS  PubMed  Google Scholar 

  70. Sagarra-Romero L. Effects of breast cancer treatment on metabolic health. Breast J. 2020;26(10):2137–8.

    Article  PubMed  Google Scholar 

  71. Saylor PJ, Keating NL, Smith MR. Prostate cancer survivorship: prevention and treatment of the adverse effects of androgen deprivation therapy. J Gen Intern Med. 2009;24(Suppl 2):S389–94.

    Article  PubMed  Google Scholar 

  72. Simon MS, et al. Cardiometabolic risk factors and survival after cancer in the Women’s Health Initiative. Cancer. 2021;127(4):598–608.

    Article  PubMed  Google Scholar 

  73. Dietz AC, et al. Risk and impact of pulmonary complications in survivors of childhood cancer: a report from the Childhood Cancer Survivor Study. Cancer. 2016;122(23):3687–96.

    Article  PubMed  Google Scholar 

  74. Ginsberg JP, et al. Long-term survivors of childhood Ewing sarcoma: report from the Childhood Cancer Survivor Study. J Natl Cancer Inst. 2010;102(16):1272–83.

    Article  PubMed  PubMed Central  Google Scholar 

  75. Huang TT, et al. Pulmonary outcomes in survivors of childhood central nervous system malignancies: a report from the Childhood Cancer Survivor Study. Pediatr Blood Cancer. 2014;61(2):319–25.

    Article  PubMed  Google Scholar 

  76. Liles A, et al. Monitoring pulmonary complications in long-term childhood cancer survivors: guidelines for the primary care physician. Cleve Clin J Med. 2008;75(7):531–9.

    Article  PubMed  Google Scholar 

  77. Mansouri I, et al. Trends and outcomes with kidney failure from antineoplastic treatments and urinary tract cancer in France. Clin J Am Soc Nephrol. 2020;15(4):484–92.

    Article  PubMed  PubMed Central  Google Scholar 

  78. Oberlin O, et al. Long-term evaluation of Ifosfamide-related nephrotoxicity in children. J Clin Oncol. 2009;27(32):5350–5.

    Article  CAS  PubMed  Google Scholar 

  79. Ehrhardt MJ, Skinner R, Castellino SM. Renal and hepatic health after childhood cancer. Pediatr Clin N Am. 2020;67(6):1203–17.

    Article  Google Scholar 

  80. Skinner R. Late renal toxicity of treatment for childhood malignancy: risk factors, long-term outcomes, and surveillance. Pediatr Nephrol. 2018;33(2):215–25.

    Article  PubMed  Google Scholar 

  81. Skinner R, Kaplan R, Nathan PC. Renal and pulmonary late effects of cancer therapy. Semin Oncol. 2013;40(6):757–73.

    Article  PubMed  Google Scholar 

  82. Dekkers IA, et al. Long-term nephrotoxicity in adult survivors of childhood cancer. Clin J Am Soc Nephrol. 2013;8(6):922–9.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  83. Jones DP, et al. Renal late effects in patients treated for cancer in childhood: a report from the Children’s Oncology Group. Pediatr Blood Cancer. 2008;51(6):724–31.

    Article  PubMed  PubMed Central  Google Scholar 

  84. Armstrong GT, et al. Long-term outcomes among adult survivors of childhood central nervous system malignancies in the Childhood Cancer Survivor Study. J Natl Cancer Inst. 2009;101(13):946–58.

    Article  PubMed  PubMed Central  Google Scholar 

  85. Balsamo LM, et al. Monitoring neurocognitive functioning in childhood cancer survivors: evaluation of CogState computerized assessment and the Behavior Rating Inventory of Executive Function (BRIEF). BMC Psychol. 2019;7(1):26.

    Article  PubMed  PubMed Central  Google Scholar 

  86. Partanen M, et al. Longitudinal trajectories of neurocognitive functioning in childhood acute lymphoblastic leukemia. J Pediatr Psychol. 2021;46(2):168–78.

    Article  PubMed  Google Scholar 

  87. Peng L, et al. Neurocognitive impairment in Asian childhood cancer survivors: a systematic review. Cancer Metastasis Rev. 2020;39(1):27–41.

    Article  CAS  PubMed  Google Scholar 

  88. Korah MP, et al. Incidence, risks, and sequelae of posterior fossa syndrome in pediatric medulloblastoma. Int J Radiat Oncol Biol Phys. 2010;77(1):106–12.

    Article  PubMed  Google Scholar 

  89. Lanier JC, Abrams AN. Posterior fossa syndrome: review of the behavioral and emotional aspects in pediatric cancer patients. Cancer. 2017;123(4):551–9.

    Article  PubMed  Google Scholar 

  90. Ross SG, et al. Cerebellar mutism after posterior fossa tumor resection: case discussion and recommendations for psychoeducational intervention. J Pediatr Oncol Nurs. 2014;31(2):78–83.

    Article  PubMed  Google Scholar 

  91. Sun LR, Cooper S. Neurological complications of the treatment of pediatric neoplastic disorders. Pediatr Neurol. 2018;85:33–42.

    Article  PubMed  Google Scholar 

  92. Reulen RC, et al. Risk of cerebrovascular disease among 13 457 five-year survivors of childhood cancer: a population-based cohort study. Int J Cancer. 2021;148(3):572–83.

    Article  CAS  PubMed  Google Scholar 

  93. El-Fayech C, et al. Cerebrovascular diseases in childhood cancer survivors: role of the radiation dose to willis circle arteries. Int J Radiat Oncol Biol Phys. 2017;97(2):278–86.

    Article  PubMed  Google Scholar 

  94. Haddy N, et al. Relationship between the brain radiation dose for the treatment of childhood cancer and the risk of long-term cerebrovascular mortality. Brain. 2011;134(Pt 5):1362–72.

    Article  PubMed  Google Scholar 

  95. Oyharcabal-Bourden V, et al. Standard-risk medulloblastoma treated by adjuvant chemotherapy followed by reduced-dose craniospinal radiation therapy: a French Society of Pediatric Oncology Study. J Clin Oncol. 2005;23(21):4726–34.

    Article  CAS  PubMed  Google Scholar 

  96. Carrie C, et al. Exclusive hyperfractionated radiation therapy and reduced boost volume for standard-risk medulloblastoma: pooled analysis of the 2 French Multicentric Studies MSFOP98 and MSFOP 2007 and Correlation With Molecular Subgroups. Int J Radiat Oncol Biol Phys. 2020;108(5):1204–17.

    Article  PubMed  Google Scholar 

  97. Orbach, D, Brisse H, Doz F. [Central neurological manifestations during chemotherapy in children]. Arch Pediatr. 2003;10(6):533–9.

    Google Scholar 

  98. Alloin AL, et al. Prevalence and risk factors of cataract after chemotherapy with or without central nervous system irradiation for childhood acute lymphoblastic leukaemia: an LEA study. Br J Haematol. 2014;164(1):94–100.

    Article  CAS  PubMed  Google Scholar 

  99. Whelan KF, et al. Ocular late effects in childhood and adolescent cancer survivors: a report from the Childhood Cancer Survivor Study. Pediatr Blood Cancer. 2010;54(1):103–9.

    Article  PubMed  PubMed Central  Google Scholar 

  100. Olivier TW, et al. Cognitive implications of ototoxicity in pediatric patients with embryonal brain tumors. J Clin Oncol. 2019;37(18):1566–75.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  101. Bass JK, et al. Evaluation and management of hearing loss in survivors of childhood and adolescent cancers: a report from the Children’s Oncology Group. Pediatr Blood Cancer. 2016;63(7):1152–62.

    Article  PubMed  PubMed Central  Google Scholar 

  102. Whelan K, et al. Auditory complications in childhood cancer survivors: a report from the Childhood Cancer Survivor Study. Pediatr Blood Cancer. 2011;57(1):126–34.

    Article  PubMed  PubMed Central  Google Scholar 

  103. Khan A, et al. The experience of hearing loss in adult survivors of childhood and young adult cancer: a qualitative study. Cancer. 2020;126(8):1776–83.

    Article  PubMed  Google Scholar 

  104. Pearson SE, et al. Cancer survivors treated with platinum-based chemotherapy affected by ototoxicity and the impact on quality of life: a narrative synthesis systematic review. Int J Audiol. 2019;58(11):685–95.

    Article  PubMed  Google Scholar 

  105. Brock PR, et al. Platinum-induced ototoxicity in children: a consensus review on mechanisms, predisposition, and protection, including a new International Society of Pediatric Oncology Boston ototoxicity scale. J Clin Oncol. 2012;30(19):2408–17.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  106. Landier W, et al. Ototoxicity in children with high-risk neuroblastoma: prevalence, risk factors, and concordance of grading scales—a report from the Children’s Oncology Group. J Clin Oncol. 2014;32(6):527–34.

    Article  PubMed  PubMed Central  Google Scholar 

  107. Bertolini P, et al. Platinum compound-related ototoxicity in children: long-term follow-up reveals continuous worsening of hearing loss. J Pediatr Hematol Oncol. 2004;26(10):649–55.

    Article  PubMed  Google Scholar 

  108. Qaddoumi I, et al. Carboplatin-associated ototoxicity in children with retinoblastoma. J Clin Oncol. 2012;30(10):1034–41.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  109. Bass JK, et al. Hearing Loss in patients who received cranial radiation therapy for childhood cancer. J Clin Oncol. 2016;34(11):1248–55.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  110. Hua C, et al. Hearing loss after radiotherapy for pediatric brain tumors: effect of cochlear dose. Int J Radiat Oncol Biol Phys. 2008;72(3):892–9.

    Article  PubMed  Google Scholar 

  111. Paulino AC, et al. Ototoxicity after intensity-modulated radiation therapy and cisplatin-based chemotherapy in children with medulloblastoma. Int J Radiat Oncol Biol Phys. 2010;78(5):1445–50.

    Article  CAS  PubMed  Google Scholar 

  112. Friedman DL, et al. Subsequent neoplasms in 5-year survivors of childhood cancer: the Childhood Cancer Survivor Study. J Natl Cancer Inst. 2010;102(14):1083–95.

    Article  PubMed  PubMed Central  Google Scholar 

  113. Turcotte LM, et al. Temporal trends in treatment and subsequent neoplasm risk among 5-year survivors of childhood cancer, 1970-2015. JAMA. 2017;317(8):814–24.

    Article  PubMed  PubMed Central  Google Scholar 

  114. Bagnasco F, et al. Late mortality and causes of death among 5-year survivors of childhood cancer diagnosed in the period 1960-1999 and registered in the Italian Off-Therapy Registry. Eur J Cancer. 2019;110:86–97.

    Article  PubMed  Google Scholar 

  115. Berger C, et al. Second malignant neoplasms following childhood cancer: a study of a recent cohort (1987-2004) from the childhood cancer registry of the Rhone-Alpes region (ARCERRA) in France. Pediatr Hematol Oncol. 2011;28(5):364–79.

    Article  PubMed  Google Scholar 

  116. Demoor-Goldschmidt C, de Vathaire F. Review of risk factors of secondary cancers among cancer survivors. Br J Radiol. 2019;92(1093):20180390.

    PubMed  Google Scholar 

  117. Bansal N, et al. Cardiovascular diseases in survivors of childhood cancer. Cancer Metastasis Rev. 2020;39(1):55–68.

    Article  PubMed  PubMed Central  Google Scholar 

  118. MacArthur AC, et al. Mortality among 5-year survivors of cancer diagnosed during childhood or adolescence in British Columbia, Canada. Pediatr Blood Cancer. 2007;48(4):460–7.

    Article  PubMed  Google Scholar 

  119. Armstrong GT, et al. Reduction in late mortality among 5-year survivors of childhood cancer. N Engl J Med. 2016;374(9):833–42.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  120. Teepen JC, et al. Long-Term risk of subsequent malignant neoplasms after treatment of childhood cancer in the DCOG LATER study cohort: role of chemotherapy. J Clin Oncol. 2017;35(20):2288–98.

    Article  CAS  PubMed  Google Scholar 

  121. Jacobson LA, Pare-Blagoev EJ, Ruble K. Barriers to schooling in survivorship: the role of neuropsychological assessment. JCO Oncol Pract. 2020;16(12):e1516–23.

    Article  PubMed  Google Scholar 

  122. van de Poll-Franse LV, et al. Perceived care and well-being of patients with cancer and matched norm participants in the COVID-19 crisis: results of a survey of participants in the dutch PROFILES registry. JAMA Oncol. 2021;7(2):279–84.

    Article  PubMed  Google Scholar 

  123. Fitch, MI, et al. Adolescent and young adult perspectives on challenges and improvements to cancer survivorship care: how are we doing? J Adolesc Young Adult Oncol. 2020.

    Google Scholar 

  124. Bjornard KL, et al. Psychosexual functioning of female childhood cancer survivors: a report from the St. Jude Lifetime Cohort Study. J Sex Med. 2020;17(10):1981–94.

    Article  PubMed  PubMed Central  Google Scholar 

  125. Thouvenin-Doulet S, et al. Fecundity and quality of life of women treated for solid childhood tumors between 1948 and 1992 in France. J Adolesc Young Adult Oncol. 2018;7(4):415–23.

    Article  PubMed  Google Scholar 

  126. Lund LW, et al. A systematic review of studies on psychosocial late effects of childhood cancer: structures of society and methodological pitfalls may challenge the conclusions. Pediatr Blood Cancer. 2011;56(4):532–43.

    Article  PubMed  Google Scholar 

  127. Michel G, Vetsch J. Screening for psychological late effects in childhood, adolescent and young adult cancer survivors: a systematic review. Curr Opin Oncol. 2015;27(4):297–305.

    Article  PubMed  Google Scholar 

  128. Abadie A, et al. Prevalence of psychiatric complications in young adults after childhood cancer treatment: results of the long-term follow-up studies in oncology. J Adolesc Young Adult Oncol. 2020;9(2):247–55.

    Article  PubMed  Google Scholar 

  129. Lubas MM, et al. Suicidality among adult survivors of childhood cancer: a report from the St. Jude Lifetime Cohort Study. Cancer. 2020;126(24):5347–55.

    Article  PubMed  Google Scholar 

  130. Oerlemans S, et al. The course of anxiety and depression for patients with Hodgkin’s lymphoma or diffuse large B cell lymphoma: a longitudinal study of the PROFILES registry. J Cancer Surviv. 2014;8(4):555–64.

    Article  PubMed  Google Scholar 

  131. Michel G, et al. Psychological distress in adult survivors of childhood cancer: the Swiss Childhood Cancer Survivor Study. J Clin Oncol. 2010;28(10):1740–8.

    Article  PubMed  Google Scholar 

  132. Gurney JG, et al. Social outcomes in the Childhood Cancer Survivor Study cohort. J Clin Oncol. 2009;27(14):2390–5.

    Article  PubMed  PubMed Central  Google Scholar 

  133. Hays DM, et al. Educational, occupational, and insurance status of childhood cancer survivors in their fourth and fifth decades of life. J Clin Oncol. 1992;10(9):1397–406.

    Article  CAS  PubMed  Google Scholar 

  134. Lancashire ER, et al. Educational attainment among adult survivors of childhood cancer in Great Britain: a population-based cohort study. J Natl Cancer Inst. 2010;102(4):254–70.

    Article  CAS  PubMed  Google Scholar 

  135. Boman KK, Lindblad F, Hjern A. Long-term outcomes of childhood cancer survivors in Sweden: a population-based study of education, employment, and income. Cancer. 2010;116(5):1385–91.

    Article  PubMed  Google Scholar 

  136. Dumas A, et al. Educational and occupational outcomes of childhood cancer survivors 30 years after diagnosis: a French cohort study. Br J Cancer. 2016;114(9):1060–8.

    Article  PubMed  PubMed Central  Google Scholar 

  137. de Boer AG, et al. Cancer survivors and unemployment: a meta-analysis and meta-regression. JAMA. 2009;301(7):753–62.

    Article  PubMed  Google Scholar 

  138. Jones JM, et al. The needs and experiences of post-treatment adolescent and young adult cancer survivors. J Clin Med. 2020;9(5):1444.

    Article  PubMed Central  Google Scholar 

  139. Mulder RL, et al. Transition guidelines: an important step in the future care for childhood cancer survivors. A comprehensive definition as groundwork. Eur J Cancer. 2016;54:64–8.

    Article  CAS  PubMed  Google Scholar 

  140. Henderson TO, Friedman DL, Meadows AT. Childhood cancer survivors: transition to adult-focused risk-based care. Pediatrics. 2010;126(1):129–36.

    Article  PubMed  Google Scholar 

  141. Denlinger CS, et al. NCCN guidelines insights: survivorship, version 2.2020. J Natl Compr Cancer Netw. 2020;18(8):1016–23.

    Article  Google Scholar 

  142. Fung C, et al. Testicular cancer survivorship. J Natl Compr Cancer Netw. 2019;17(12):1557–68.

    Article  CAS  Google Scholar 

  143. Lokich E. Gynecologic cancer survivorship. Obstet Gynecol Clin N Am. 2019;46(1):165–78.

    Article  Google Scholar 

  144. Signorelli C, et al. Models of childhood cancer survivorship care in Australia and New Zealand: strengths and challenges. Asia Pac J Clin Oncol. 2017;13(6):407–15.

    Article  PubMed  Google Scholar 

  145. Nekhlyudov L, et al. Head and neck cancer survivorship care guideline: American Society of Clinical Oncology Clinical Practice Guideline Endorsement of the American Cancer Society Guideline. J Clin Oncol. 2017;35(14):1606–21.

    Article  PubMed  Google Scholar 

  146. Kinahan KE, et al. Models of cancer survivorship care for adolescents and young adults. Semin Oncol Nurs. 2015;31(3):251–9.

    Article  PubMed  PubMed Central  Google Scholar 

  147. Tonorezos ES, Henderson TO. Clinical guidelines for the care of childhood cancer survivors. Children (Basel). 2014;1(2):227–40.

    Google Scholar 

  148. Gilbert SM, et al. Cancer survivorship: challenges and changing paradigms. J Urol. 2008;179(2):431–8.

    Article  PubMed  PubMed Central  Google Scholar 

  149. Berger C, et al. Objectives and organization for the long-term follow-up after childhood cancer. Bull Cancer. 2015;102(7–8):579–85.

    Article  PubMed  Google Scholar 

  150. Demoor-Goldschmidt C, Bernier V. [Towards an improvement of the quality of life after radiotherapy in children]. Bull Cancer. 2015;102(7–8):674–83.

    Google Scholar 

  151. Kremer LC, et al. A worldwide collaboration to harmonize guidelines for the long-term follow-up of childhood and young adult cancer survivors: a report from the International Late Effects of Childhood Cancer Guideline Harmonization Group. Pediatr Blood Cancer. 2013;60(4):543–9.

    Article  PubMed  Google Scholar 

  152. Landier W, et al. Development of risk-based guidelines for pediatric cancer survivors: the Children’s Oncology Group Long-Term Follow-Up Guidelines from the Children’s Oncology Group Late Effects Committee and Nursing Discipline. J Clin Oncol. 2004;22(24):4979–90.

    Article  PubMed  Google Scholar 

  153. Oeffinger KC, Hudson MM, Landier W. Survivorship: childhood cancer survivors. Prim Care. 2009;36(4):743–80.

    Article  PubMed  Google Scholar 

  154. Poplack DG, et al. Childhood cancer survivor care: development of the Passport for Care. Nat Rev Clin Oncol. 2014;11(12):740–50.

    Article  PubMed  PubMed Central  Google Scholar 

  155. Brown MC, et al. The views of European clinicians on guidelines for long-term follow-up of childhood cancer survivors. Pediatr Blood Cancer. 2015;62(2):322–8.

    Article  PubMed  Google Scholar 

  156. Byrne J, et al. The PanCareSurFup consortium: research and guidelines to improve lives for survivors of childhood cancer. Eur J Cancer. 2018;103:238–48.

    Article  PubMed  Google Scholar 

  157. Gatta G, et al. Patterns of care for European colorectal cancer patients diagnosed 1996-1998: a EUROCARE high resolution study. Acta Oncol. 2010;49(6):776–83.

    Article  PubMed  Google Scholar 

  158. Haupt R, et al. The ‘Survivorship Passport’ for childhood cancer survivors. Eur J Cancer. 2018;102:69–81.

    Article  PubMed  Google Scholar 

  159. Michel G, et al. Evidence-based recommendations for the organization of long-term follow-up care for childhood and adolescent cancer survivors: a report from the PanCareSurFup Guidelines Working Group. J Cancer Surviv. 2019;13(5):759–72.

    Article  PubMed  Google Scholar 

  160. Skinner R, Oeffinger KC. Developing international consensus for late effects screening and guidance. Curr Opin Support Palliat Care. 2013;7(3):303–8.

    Article  PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Charlotte Demoor-Goldschmidt .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2021 Springer Nature Switzerland AG

About this chapter

Check for updates. Verify currency and authenticity via CrossMark

Cite this chapter

Contant, P., Demoor-Goldschmidt, C. (2021). Specific Issues of Children and Young Adults in Survivorship Care. In: Rauh, S. (eds) Survivorship Care for Cancer Patients. Springer, Cham. https://doi.org/10.1007/978-3-030-78648-9_16

Download citation

  • DOI: https://doi.org/10.1007/978-3-030-78648-9_16

  • Published:

  • Publisher Name: Springer, Cham

  • Print ISBN: 978-3-030-78647-2

  • Online ISBN: 978-3-030-78648-9

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics