Imatinib alternating with regorafenib compared to imatinib alone for the first-line treatment of advanced gastrointestinal stromal tumor: The AGITG ALT-GIST intergroup randomized phase II trial.

IF 6.4 1区 医学 Q1 ONCOLOGY
Desmond Yip, John Zalcberg, Jean-Yves Blay, Mikael Eriksson, David Espinoza, Timothy Price, Sandrine Marreaud, Antoine Italiano, Neeltje Steeghs, Kjetil Boye, Craig Underhill, Val Gebski, John Simes, Hans Gelderblom, Heikki Joensuu
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引用次数: 0

Abstract

Background: To determine if an alternating regimen of the tyrosine kinase inhibitors imatinib and regorafenib improved outcomes in patients with advanced gastrointestinal stromal tumors.

Methods: ALTGIST (NCT02365441) was a randomized phase II study of standard treatment of imatinib (Arm A) compared with an experimental alternating regimen of imatinib and regorafenib (Arm B). Primary outcome was best objective tumor response (OTR) at nine months.

Results: Seventy-six eligible patients (Arm A 36, Arm B 40) enrolled were evaluable. Median follow-up was 46.0 months (range 6.5-64.6). Best responses and OTR were similar at 9 months. Eighteen (50.0%) Arm A patients and twelve (30.0%) Arm B patients discontinued treatment due to progressive disease. No Arm A patients stopped protocol therapy due to unacceptable toxicity, with 12 (30.0%) stopping in Arm B. Twelve (33.2%) Arm A patients and 12 (30.0%) Arm B patients experienced at least one serious adverse event, mostly grade 3. Secondary endpoints of PFS at 1 and OS at 1 year were not statistically different.

Conclusions: Alternation of imatinib and regorafenib did not impact on 9 months objective response nor on the secondary objectives of PFS and OS. Patients in the alternating arm experienced more toxicity and protocol discontinuations.

Clinical trial registration: NCT02365441.

与单独使用伊马替尼相比,伊马替尼交替使用瑞戈非尼治疗晚期胃肠道间质瘤的一线治疗:AGITG ALT-GIST组间随机II期试验
背景:确定酪氨酸激酶抑制剂伊马替尼和瑞戈非尼交替治疗方案是否能改善晚期胃肠道间质瘤患者的预后。方法:ALTGIST (NCT02365441)是一项随机II期研究,将伊马替尼(a组)的标准治疗与伊马替尼和瑞非尼(B组)的实验性交替治疗进行比较。主要结局是9个月时的最佳客观肿瘤反应(OTR)。结果:纳入的76例符合条件的患者(A组36例,B组40例)可评估。中位随访时间为46.0个月(6.5-64.6个月)。在9个月时,最佳疗效和OTR相似。18例(50.0%)A组患者和12例(30.0%)B组患者因疾病进展而停止治疗。没有A组患者因不可接受的毒性而停止方案治疗,12名(30.0%)患者在B组停止治疗,12名(33.2%)A组患者和12名(30.0%)B组患者经历了至少一次严重不良事件,大多数为3级。1年PFS和1年OS的次要终点无统计学差异。结论:伊马替尼和瑞非尼交替使用对9个月的客观反应没有影响,也没有影响PFS和OS的次要目标。交替治疗组的患者经历了更多的毒性和方案中断。临床试验注册:NCT02365441。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
British Journal of Cancer
British Journal of Cancer 医学-肿瘤学
CiteScore
15.10
自引率
1.10%
发文量
383
审稿时长
6 months
期刊介绍: The British Journal of Cancer is one of the most-cited general cancer journals, publishing significant advances in translational and clinical cancer research.It also publishes high-quality reviews and thought-provoking comment on all aspects of cancer prevention,diagnosis and treatment.
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