主旨
舒尼替尼
医学
瑞戈非尼
伊马替尼
间质瘤
肿瘤科
内科学
甲磺酸伊马替尼
PDGFRA公司
川东北117
结直肠癌
癌症
间质细胞
川地34
生物
干细胞
遗传学
髓系白血病
作者
Ciara M. Kelly,L. Gutiérrez Sainz,Ping Chi
标识
DOI:10.1186/s13045-020-01026-6
摘要
Gastrointestinal stromal tumor (GIST) is the most common mesenchymal tumor of the gastrointestinal tract. The majority of GISTs harbor gain of function mutations in either KIT or PDGFRα. Determination of the GIST molecular subtype upon diagnosis is important because this information informs therapeutic decisions in both the adjuvant and metastatic setting. The management of GIST was revolutionized by the introduction of imatinib, a KIT inhibitor, which has become the standard first line treatment for metastatic GIST. However, despite a clinical benefit rate of 80%, the majority of patients with GIST experience disease progression after 2-3 years of imatinib therapy. Second and third line options include sunitinib and regorafenib, respectively, and yield low response rates and limited clinical benefit. There have been recent FDA approvals for GIST including ripretinib in the fourth-line setting and avapritinib for PDGFRA exon 18-mutant GIST. This article aims to review the optimal treatment approach for the management of patients with advanced GIST. It examines the standard treatment options available but also explores the novel treatment approaches in the setting of imatinib refractory GIST.
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