Recent advances in the treatment of gastrointestinal stromal tumors

被引:53
|
作者
Serrano, Cesar [1 ]
George, Suzanne [1 ]
机构
[1] Harvard Univ, Sch Med, Dana Farber Canc Inst, Ctr Sarcoma & Bone Oncol, Boston, MA 02215 USA
关键词
c-KIT; gastrointestinal stromal tumors; imatinib; masitinib; nilotinib; regorafenib; sorafenib; sunitinib; PHASE-II TRIAL; IMATINIB MESYLATE; TYROSINE KINASE; SUCCINATE-DEHYDROGENASE; ACQUIRED-RESISTANCE; ADJUVANT IMATINIB; DOSE IMATINIB; KIT; INHIBITOR; MUTATIONS;
D O I
10.1177/1758834014522491
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Constitutively activating mutations in the KIT and platelet-derived growth factor receptor alpha (PDGFRA) RTKs play a crucial role in the biology of gastrointestinal stromal tumors (GISTs), and this disease has served as an effective model for targeting gain-of-function kinase mutations in cancer. Imatinib has entered the clinical arena in the last decade and substantially improved the outcome in these formerly untreatable cancers. However, most advanced GISTs responding to imatinib progress within 2-3 years due to heterogeneous subclones harboring a range of imatinib-resistant secondary KIT mutations. Sunitinib, and more recently, regorafenib, have obtained US Food and Drug Administration approval for the treatment of GISTs after imatinib failure, and thus expanded the treatment options in resistant disease. Within this framework, we present an evaluation of current GIST management, emphasizing the most recent advances in the field together with a discussion on future steps to be taken in refractory disease.
引用
收藏
页码:115 / 127
页数:13
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