医学
舒尼替尼
临床终点
内科学
主旨
人口
无进展生存期
肿瘤科
意向治疗分析
外科
不利影响
胃肠病学
总体生存率
随机对照试验
间质细胞
癌症
环境卫生
作者
Michael C. Heinrich,Jean‐Yves Blay,Hans Gelderblom,Suzanne George,Patrick Schöffski,Margaret von Mehren,John Zalcberg,Robin L. Jones,Yoon‐Koo Kang,Albiruni R. Abdul Razak,Jonathan C. Trent,Steven Attia,Axel Le Cesne,Kjetil Boye,David Goldstein,César Sánchez,Brittany L. Siontis,P. H. Cox,Erika Davis,Matthew L. Sherman
摘要
In the INTRIGUE phase III trial (ClinicalTrials.gov identifier: NCT03673501 ), adult patients with advanced gastrointestinal stromal tumor previously treated with imatinib were randomly assigned 1:1 to ripretinib 150 mg once daily or sunitinib 50 mg once daily (4 weeks on/2 weeks off). In the primary analysis, overall survival (OS) was immature. In this study, we report the final planned analysis of OS (key secondary end point), progression-free survival (PFS) on third-line therapy (second PFS; prespecified exploratory end point), and long-term safety. Final OS analysis was prespecified to occur with approximately 200 and ≥145 events in the overall and KIT exon 11 intention-to-treat (ITT) populations, respectively. As of March 15, 2023, there were 211 and 151 OS events in the overall ITT and KIT exon 11 ITT populations, respectively. Median OS was similar between second-line ripretinib and sunitinib in both populations (overall, 35.5 v 31.5 months; KIT exon 11, 35.5 v 32.8 months). Median second PFS (on third-line therapy) for the overall ITT population was similar between the ripretinib and sunitinib arms (7.7 v 7.4 months). Safety was consistent with the primary analysis. OS from this analysis was similar between arms, and second PFS suggests that receiving ripretinib did not adversely affect the PFS of third-line therapy.
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