Suppr超能文献

一项关于阿伐替尼联合铂类依托泊苷化疗用于铂难治性小细胞肺癌患者的2期开放标签多中心研究。

A phase 2, open-label, multi-center study of amuvatinib in combination with platinum etoposide chemotherapy in platinum-refractory small cell lung cancer patients.

作者信息

Byers Lauren Averett, Horn Leora, Ghandi Jitendra, Kloecker Goetz, Owonikoko Taofeek, Waqar Saiama Naheed, Krzakowski Maciej, Cardnell Robert J, Fujimoto Junya, Taverna Pietro, Azab Mohammad, Camidge David Ross

机构信息

University of Texas, M.D. Anderson Cancer Center, Houston, TX, USA.

Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN, USA.

出版信息

Oncotarget. 2017 Aug 3;8(46):81441-81454. doi: 10.18632/oncotarget.19888. eCollection 2017 Oct 6.

Abstract

BACKGROUND

Amuvatinib (MP-470) is a multi-targeted kinase inhibitor with potent activity against c-Kit, synergistic with DNA-damaging agents. We evaluated amuvatinib in combination with platinum-etoposide (EP) chemotherapy by objective response rate, survival, and tolerability in platinum-refractory small cell lung cancer (SCLC) patients.

METHODS

This study used a Simon 2-stage design requiring ≥3 centrally confirmed responses in the first 21 subjects. Subjects received EP with 300 mg amuvatinib orally three times daily in cycles of 21 days. A three-day amuvatinib run-in period before EP occurred in Cycle 1. Subjects received the same EP chemotherapy regimen given prior to progression/relapse.

RESULTS

Among 23 subjects treated, we observed four PRs (17.4%) per RECIST 1.1, only two of which were centrally confirmed (8.7%, response duration 119, 151 days). Three subjects (13%) had confirmed stable disease. c-Kit H-score was ≥100 in two subjects whose respective durations of disease control were 151 and 256 days.

CONCLUSIONS

The addition of amuvatinib to EP chemotherapy in unselected, platinum-refractory SCLC did not meet the primary endpoint of ≥3 confirmed responses in stage 1. However, high c-Kit expression in two subjects with durable disease control suggests the potential for further study of amuvatinib in SCLC patients with high c-Kit expression.

摘要

背景

阿幕瓦替尼(MP-470)是一种多靶点激酶抑制剂,对c-Kit具有强效活性,与DNA损伤剂具有协同作用。我们通过客观缓解率、生存率和耐受性,评估了阿幕瓦替尼联合铂-依托泊苷(EP)化疗方案在铂难治性小细胞肺癌(SCLC)患者中的疗效。

方法

本研究采用Simon两阶段设计,要求在前21名受试者中至少有3例经中心确认的缓解。受试者接受EP化疗,并口服阿幕瓦替尼300mg,每日3次,每21天为一个周期。在第1周期的EP化疗前有一个为期3天的阿幕瓦替尼导入期。受试者接受疾病进展/复发前使用的相同EP化疗方案。

结果

在接受治疗的23名受试者中,根据RECIST 1.1标准,我们观察到4例部分缓解(PR)(17.4%),其中只有2例经中心确认(8.7%,缓解持续时间分别为119天和151天)。3名受试者(13%)疾病稳定。2名c-Kit H评分≥100的受试者,其疾病控制持续时间分别为151天和256天。

结论

在未经选择的铂难治性SCLC患者中,EP化疗联合阿幕瓦替尼未达到第1阶段至少3例经确认缓解的主要终点。然而,2例疾病控制持久的受试者中c-Kit高表达,提示阿幕瓦替尼在c-Kit高表达的SCLC患者中具有进一步研究的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0aee/5655298/4f2e65f0f27d/oncotarget-08-81441-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验