Imatinib resistance in gastrointestinal stromal tumors |
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Authors: | Lei L. Chen Mahyar Sabripour Robert H. I. Andtbacka Shreyaskumar R. Patel Barry W. Feig Homer A. Macapinlac Haesun Choi Elsie F. Wu Marsha L. Frazier Robert S. Benjamin |
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Affiliation: | (1) Department of Sarcoma, The University of Texas M.D. Anderson Cancer Center, 1515 Holcombe Boulevard, 77030 Houston, TX, USA |
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Abstract: | Conventional chemotherapeutic drugs are ineffective in treatment of gastrointestinal stromal tumors (GISTs). Imatinib (STI571, Gleevec, Glivec; Novartis Pharmaceuticals, East Hanover, NJ), a selective inhibitor of KIT, ABL, BCR-ABL, PDGFRA, and PDGFRB, represents a new paradigm of targeted cancer therapy and has revolutionized the treatment of patients with chronic myelogenous leukemia and GISTs. Unfortunately, imatinib resistance has emerged. The reported mechanism of imatinib resistance in GISTs involves missense mutation in the kinase domain of KIT, including Thr670Ile, Tyr823Asp, and Val654Ala. The established mechanisms and potential mechanisms of imatinib resistance in GISTs, the imaging studies indicative of early development of imatinib resistance, and the management of imatinib-resistant GISTs are discussed. |
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