Abstract
Pediatric malignancies are markedly different from adult tumors, and the differences, along with a more concerted treatment network than typical for adult oncology, account for the significantly better survival rates and outcomes. The first reason is probably the different type of tumors which occurs in pediatrics. The solid malignancies of childhood are typically rapidly proliferating noncarcinomatous tumors, and the leukemias are clonal proliferation of early lymphoid progenitors. Both typically, harbor few if any genetic abnormalities. The slow-growing carcinomatous neoplasms, so characteristic of adulthood, are uncommon in pediatric oncology, and viruses, environmental toxins, and carcinogens appear, in general, to play a lesser role. Accordingly, when a child presents with a tumor where the accumulation of genetic changes rekindles a clonal carcinogenesis model reminiscent of adult carcinoma (1), the prognosis is usually very poor.
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Klement, G., Kerbel, R.S. (2003). Targeting Oncogenes in Pediatric Malignancies. In: Rak, J. (eds) Oncogene-Directed Therapies. Cancer Drug Discovery and Development. Humana Press, Totowa, NJ. https://doi.org/10.1007/978-1-59259-313-2_19
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