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优化甲磺酸伊马替尼在胃肠道间质瘤中的治疗

Optimizing imatinib mesylate treatment in gastrointestinal stromal tumors.

作者信息

Jiang Yixing, Ming Lee, Montero Alberto J, Kimchi Eric, Nikfarjam Mehrdad, Staveley-O'Carroll Kevin F

机构信息

Department of Medicine, Hematology/Oncology Division, Penn State University, Hershey Medical Center, Hershey, PA.

出版信息

Gastrointest Cancer Res. 2008 Sep;2(5):245-50.

Abstract

Improvements in the understanding of molecular oncogenesis and mechanisms of drug resistance have presented new opportunities for the treatment of gastrointestinal stromal tumors (GIST). In particular, the discovery of c-kit genomic mutations in GIST and the development of targeted therapy with imatinib mesylate and sunitinib have heralded a new era in the treatment of this disease. Due to its high activity in GIST, imatinib has become the standard of care in treating both advanced disease and localized disease with high-risk features. On the other hand, these developments have provided new challenges in optimizing the use of our drug armamentarium in conjunction with surgery. This review focuses on the molecular oncogenesis of GIST and provides a summary of recent approaches in the management of this disease.

摘要

对分子肿瘤发生机制和耐药机制认识的提高为胃肠道间质瘤(GIST)的治疗带来了新机遇。特别是,GIST中c-kit基因变异的发现以及甲磺酸伊马替尼和舒尼替尼靶向治疗的发展开创了该疾病治疗的新纪元。由于伊马替尼在GIST中具有高活性,它已成为治疗晚期疾病和具有高危特征的局限性疾病的标准治疗方法。另一方面,这些进展在优化药物与手术联合应用方面带来了新挑战。本综述聚焦于GIST的分子肿瘤发生机制,并总结了该疾病管理的最新方法。

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