舒尼替尼
医学
伊马替尼
酪氨酸激酶抑制剂
主旨
PDGFRA公司
间质瘤
临床终点
肿瘤科
间质细胞
内科学
甲磺酸伊马替尼
临床试验
临床研究阶段
酪氨酸激酶
瑞戈非尼
癌症研究
癌症
受体
结直肠癌
髓系白血病
作者
John Nemunaitis,Sebastian Bauer,Jean‐Yves Blay,Khalil Choucair,Hans Gelderblom,Suzanne George,Patrick Schöffski,Margaret von Mehren,John Zalcberg,Haroun Achour,Rodrigo Ruiz‐Soto,Michael C. Heinrich
出处
期刊:Future Oncology
[Future Medicine]
日期:2019-11-22
卷期号:16 (1): 4251-4264
被引量:52
标识
DOI:10.2217/fon-2019-0633
摘要
Ripretinib (DCC-2618) is a novel, type II tyrosine switch control inhibitor designed to broadly inhibit activating and drug-resistant mutations in KIT and PDGFRA. Ripretinib has emerged as a promising investigational agent for the treatment of gastrointestinal stromal tumor owing to targeted inhibition of secondary resistance mutations that may develop following treatment with prior line(s) of tyrosine kinase inhibitors. Here we describe the rationale and design of intrigue (NCT03673501), a global, randomized (1:1), open-label, Phase III study comparing the safety and efficacy of ripretinib versus sunitinib in patients with advanced gastrointestinal stromal tumor following imatinib. The primary end point is progression-free survival and key secondary objectives include objective response rate and overall survival. Clinical Trial Registration: NCT03673501
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