TY - JOUR
T1 - Challenges and opportunities for childhood cancer drug development
AU - Houghton, Peter J.
AU - Kurmasheva, Raushan T.
N1 - Funding Information:
Address correspondence to: Dr. Peter J. Houghton, Greehey Children’s Cancer Research Institute, University of Texas Health, San Antonio, TX 78229. E-mail: HoughtonP@uthscsa.edu This work was supported by National Institutes of Health National Cancer Institute [Grants N01-CM4226, U01 CA199297, CA169368, and CA165995]. Cancer Prevention and Research Institute of Texas (CPRIT) [Grant RP160716]. Original work presented or referenced was supported by National Cancer Institute [Grants CA23099, CA77776, CA169368, CA165995, N01CA42216, and U01CA199297]. https://doi.org/10.1124/pr.118.016972.
Funding Information:
This work was supported by National Institutes of Health National Cancer Institute [Grants N01-CM4226, U01 CA199297, CA169368, and CA165995]. Cancer Prevention and Research Institute of Texas (CPRIT) [Grant RP160716]. Original work presented or referenced was supported by National Cancer Institute [Grants CA23099, CA77776, CA169368, CA165995, N01CA42216, and U01CA199297].
Publisher Copyright:
© 2019, American Society for Pharmacology and Experimental Therapy. All rights reserved.
PY - 2019/10/1
Y1 - 2019/10/1
N2 - 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, therapyrelated 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 highrisk cancers, significant challenges remain.
AB - 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, therapyrelated 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 highrisk cancers, significant challenges remain.
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U2 - 10.1124/pr.118.016972
DO - 10.1124/pr.118.016972
M3 - Article
C2 - 31558580
AN - SCOPUS:85072715646
SN - 0031-6997
VL - 71
SP - 671
EP - 697
JO - Pharmacological Reviews
JF - Pharmacological Reviews
IS - 4
ER -