Abstract
This chapter will discuss Wilms’ tumor, neuroblastoma, rhabdomyosarcoma, Ewing’s sarcoma, pediatric Hodgkin’s disease, and retinoblastoma. The number one cause of death in children is accidents (44%), followed by cancer (10%), congenital abnormalities (8%), homicide (5%), and heart disease (4%). Of childhood cancers, leukemias are the most common (∼30%, the majority of which are ALL) followed by CNS neoplasms (∼20%), lymphomas (∼15%, Hodgkin’s > NHL > Burkitt’s lymphoma), neuroblastoma (∼8%), Wilms’ tumor (∼6%), osteosarcoma (∼3%), rhabdomyosarcoma (∼3%), nonrhabdomyosarcoma soft-tissue sarcomas (∼3%), Ewing’s sarcoma (∼2%), retinoblastoma (∼2%), and others. Of pediatric CNS neoplasms, gliomas are most common (low-grade astrocytomas ∼35–50%, brainstem gliomas ∼15%, malignant astrocytomas ∼10%, optic pathway gliomas ∼5%), followed by medulloblastoma (∼20%), ependymomas (∼10%), craniopharyngioma (∼5–10%), and germ cell tumors (<5%). These are discussed in (Chapter 2). Whenever possible, we recommend that children be enrolled in cooperative group protocols.
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References
Wilms’Tumor
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Neuroblastoma
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Rhabdomyosarcoma
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Ewing’S sarcoma
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Pediatric Hodgkin’s Lymphoma
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Retinoblastoma
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Further Reading
Bleyer WA. The U.S. pediatric cancer clinical trials programmes: international implications and the way forward. Eur J Cancer 1997;33:1439-1447.
Faria P, Beckwidth JB, Mishra K, et al. Focal versus diffuse anaplasia in Wilms Tumor: New definitions with prognostic significance. A Report from the National Wilms Tumor Study Group. Am J Surg Pathol 1996;20:909-920.
George RE, London WB, Cohn SL, et al. Hyperdiploidy plus nonamplified MYCN confers a favorable prognosis in children 12 to 18 months old with disseminated neuroblastoma: A Pediatric Oncology Group Study. J Clin Oncol 2005;23:6466-6473.
Halperin EC. Wilms’ Tumor. In: Halperin EC, Constine LS, Tarbell NJ, et al., editors. Pediatric radiation oncology. 4th ed. Philadelphia, PA: Lippincott Williams & Wilkins; 2005. pp. 379-422.
Kalapurakal J, Thomas PRM. Wilms’ Tumor. In: Perez CA, Brady LW, Halperin EC, et al., editors. Principles and practice of radiation oncology. 5th ed. Philadelphia: Lippincott Williams & Wilkins; 2008. pp. 1850-1858.
Kalapurakal J, Thomas PRM. Wilms’ Tumor. In: Gunderson LL, Tepper JE, editors. Clinical radiation oncology, 2nd ed. Philadelphia: Churchill Livingston; 2007. pp 1613-1623.
Kun LE. Childhood Cancer. In: Cox JD, Ang KK, editors. Radiation oncology: rationale, technique, results. 8th ed. St. Louis: Mosby; 2003. pp. 913-938.
Spierer M, Tereffe W, Wolden S. Neuroblastoma and Wilms’ Tumor. In: Leibel SA, Phillips TL, editors. Textbook of radiation oncology. 2nd ed. Philadelphia: Saunders; 2004. pp. 1273-1298.
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Tsuji, S.Y., Chan, L.W., Haas-Kogan, D.A. (2010). Pediatric (Non-CNS) Tumors. In: Hansen, E., Roach, M. (eds) Handbook of Evidence-Based Radiation Oncology. Springer, New York, NY. https://doi.org/10.1007/978-0-387-92988-0_41
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