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Challenges and Opportunities for Childhood Cancer Drug Development

Journal

PHARMACOLOGICAL REVIEWS
Volume 71, Issue 4, Pages 671-697

Publisher

AMER SOC PHARMACOLOGY EXPERIMENTAL THERAPEUTICS
DOI: 10.1124/pr.118.016972

Keywords

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Funding

  1. National Institutes of Health National Cancer Institute [N01-CM4226, U01 CA199297, CA169368, CA165995]
  2. Cancer Prevention and Research Institute of Texas (CPRIT) [RP160716]
  3. National Cancer Institute [CA169368, CA165995, CA23099, CA77776, N01CA42216, U01CA199297]

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Cancer in children is rare with approximately 15,700 new cases diagnosed in the United States annually. Through use of multimodality therapy (surgery, radiation therapy, and aggressive chemotherapy), 70% of patients will be cured of their disease, and 5-year event-free survival exceeds 80%. However, for patients surviving their malignancy, therapy-related long-term adverse effects are severe, with an estimated 50% having chronic life-threatening toxicities related to therapy in their fourth or fifth decade of life. While overall intensive therapy with cytotoxic agents continues to reduce cancer-related mortality, new understanding of the molecular etiology of many childhood cancers offers an opportunity to redirect efforts to develop effective, less genotoxic therapeutic options, including agents that target oncogenic drivers directly, and the potential for use of agents that target the tumor microenvironment and immune-directed therapies. However, for many high-risk cancers, significant challenges remain.

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