Trifluridine-Tipiracil with and without Bevacizumab in Colorectal Cancer.

IF 11.6
NEJM evidence Pub Date : 2026-03-01 Epub Date: 2026-02-24 DOI:10.1056/EVIDoa2500120
Maliha Nusrat, Ruizhi Zhao, Nadeem Khan, Yuexi Wang, Kathryn L Penney, Christopher G Cann, Tehseen Salimi
{"title":"Trifluridine-Tipiracil with and without Bevacizumab in Colorectal Cancer.","authors":"Maliha Nusrat, Ruizhi Zhao, Nadeem Khan, Yuexi Wang, Kathryn L Penney, Christopher G Cann, Tehseen Salimi","doi":"10.1056/EVIDoa2500120","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>In the phase 3 SUNLIGHT trial (Study of Trifluridine/Tipiracil With and Without Bevacizumab in Refractory Metastatic Colorectal Cancer Patients), trifluridine-tipiracil+bevacizumab (FTD-TPI+bev) improved the overall survival of patients with metastatic colorectal cancer (mCRC) compared with trifluridine-tipiracil (FTD-TPI) monotherapy. We investigated the real-world outcomes of FTD-TPI+bev compared with FTD-TPI for patients with mCRC.</p><p><strong>Methods: </strong>We analyzed U.S.-based electronic medical records and claims in the ConcertAI RWD360 dataset. Adults with mCRC were grouped by first exposure to FTD-TPI versus FTD-TPI+bev. Propensity score matching was used to balance the cohorts based on patient characteristics. Kaplan-Meier analyses were used to describe the real-world overall survival (rwOS, the primary outcome), time to treatment discontinuation (rwTTD), and time to next treatment or death (rwTTNTD).</p><p><strong>Results: </strong>This cohort included 3151 patients treated with FTD-TPI and 529 patients treated with FTD-TPI+bev. After propensity score matching, 472 patients were included in each cohort with balanced patient characteristics. The median rwOS was 8.9 months (95% confidence interval [CI], 7.8 to 10.1) for FTD-TPI+bev and 5.8 months (95% CI, 4.9 to 6.7) for FTD-TPI (P<0.001). The median rwTTD was 3.5 months (95% CI, 3.2 to 3.8) in the FTD-TPI+bev group and 2.2 months (95% CI, 1.9 to 2.5) in the FTD-TPI group. The median rwTTNTD among the FTD-TPI+bev group was 4.9 months (95% CI, 4.5 to 5.4) and in the FTD-TPI group it was 3.5 months (95% CI, 3.1 to 3.7).</p><p><strong>Conclusions: </strong>This U.S.-based real-world observational study found that FTD-TPI+bev was associated with longer rwOS compared with FTD-TPI in patients with mCRC. These findings align with the results of the SUNLIGHT clinical trial. (Funded by Taiho Oncology, Inc. and others.).</p>","PeriodicalId":74256,"journal":{"name":"NEJM evidence","volume":"5 3","pages":"EVIDoa2500120"},"PeriodicalIF":11.6000,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"NEJM evidence","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1056/EVIDoa2500120","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/24 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: In the phase 3 SUNLIGHT trial (Study of Trifluridine/Tipiracil With and Without Bevacizumab in Refractory Metastatic Colorectal Cancer Patients), trifluridine-tipiracil+bevacizumab (FTD-TPI+bev) improved the overall survival of patients with metastatic colorectal cancer (mCRC) compared with trifluridine-tipiracil (FTD-TPI) monotherapy. We investigated the real-world outcomes of FTD-TPI+bev compared with FTD-TPI for patients with mCRC.

Methods: We analyzed U.S.-based electronic medical records and claims in the ConcertAI RWD360 dataset. Adults with mCRC were grouped by first exposure to FTD-TPI versus FTD-TPI+bev. Propensity score matching was used to balance the cohorts based on patient characteristics. Kaplan-Meier analyses were used to describe the real-world overall survival (rwOS, the primary outcome), time to treatment discontinuation (rwTTD), and time to next treatment or death (rwTTNTD).

Results: This cohort included 3151 patients treated with FTD-TPI and 529 patients treated with FTD-TPI+bev. After propensity score matching, 472 patients were included in each cohort with balanced patient characteristics. The median rwOS was 8.9 months (95% confidence interval [CI], 7.8 to 10.1) for FTD-TPI+bev and 5.8 months (95% CI, 4.9 to 6.7) for FTD-TPI (P<0.001). The median rwTTD was 3.5 months (95% CI, 3.2 to 3.8) in the FTD-TPI+bev group and 2.2 months (95% CI, 1.9 to 2.5) in the FTD-TPI group. The median rwTTNTD among the FTD-TPI+bev group was 4.9 months (95% CI, 4.5 to 5.4) and in the FTD-TPI group it was 3.5 months (95% CI, 3.1 to 3.7).

Conclusions: This U.S.-based real-world observational study found that FTD-TPI+bev was associated with longer rwOS compared with FTD-TPI in patients with mCRC. These findings align with the results of the SUNLIGHT clinical trial. (Funded by Taiho Oncology, Inc. and others.).

trifluriddine - tipiracil联合或不联合贝伐单抗治疗结直肠癌。
背景:在3期SUNLIGHT试验(Trifluridine/Tipiracil联合和不联合贝伐单抗治疗难治性转移性结直肠癌患者的研究)中,与Trifluridine - Tipiracil (FTD-TPI)单药治疗相比,Trifluridine - Tipiracil + Bevacizumab (FTD-TPI+bev)改善了转移性结直肠癌(mCRC)患者的总生存期。我们研究了FTD-TPI+与FTD-TPI对mCRC患者的实际结果的比较。方法:我们分析了ConcertAI RWD360数据集中美国的电子医疗记录和索赔。根据首次暴露于FTD-TPI和FTD-TPI+的情况对mCRC成人进行分组。根据患者特征使用倾向评分匹配来平衡队列。Kaplan-Meier分析用于描述真实世界的总生存期(rwOS,主要结局)、到停止治疗的时间(rwTTD)以及到下一次治疗或死亡的时间(rwTTNTD)。结果:该队列包括3151例FTD-TPI患者和529例FTD-TPI+bev患者。倾向评分匹配后,每组纳入472例患者,患者特征平衡。FTD-TPI+bev的中位rwOS为8.9个月(95%可信区间[CI], 7.8至10.1),FTD-TPI的中位rwOS为5.8个月(95%可信区间[CI], 4.9至6.7)。结论:这项基于美国的真实世界观察性研究发现,与FTD-TPI相比,mCRC患者的FTD-TPI+bev与更长的rwOS相关。这些发现与SUNLIGHT临床试验的结果一致。(由Taiho Oncology, Inc.等资助)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书