Lenvatinib Plus Pembrolizumab Versus Standard of Care for Previously Treated Metastatic Colorectal Cancer: Final Analysis of the Randomized, Open-Label, Phase III LEAP-017 Study.

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-08-20 Epub Date: 2024-06-04 DOI:10.1200/JCO.23.02736
Akihito Kawazoe, Rui-Hua Xu, Pilar García-Alfonso, Maria Passhak, Hao-Wei Teng, Ardaman Shergill, Mahmut Gumus, Camilla Qvortrup, Sebastian Stintzing, Kathryn Towns, Tae Won Kim, Kai Keen Shiu, Juan Cundom, Sumitra Ananda, Andrey Lebedinets, Rong Fu, Rishi Jain, David Adelberg, Volker Heinemann, Takayuki Yoshino, Elena Elez
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Abstract

Purpose: Treatment options are limited for patients with previously treated metastatic colorectal cancer (mCRC). In the LEAP-017 study, we evaluate whether lenvatinib in combination with pembrolizumab improves outcomes compared with standard of care (SOC) in previously treated mismatch repair proficient or not microsatellite instability high (pMMR or not MSI-H) mCRC.

Methods: In this international, multicenter, randomized, controlled, open-label, phase III study, eligible patients age 18 years and older with unresectable, pMMR or not MSI-H mCRC, that had progressed on or after, or could not tolerate, standard treatment, were randomly assigned 1:1 to lenvatinib 20 mg orally once daily plus pembrolizumab 400 mg intravenously once every 6 weeks or investigator's choice of regorafenib or trifluridine/tipiracil (SOC). Randomization was stratified by presence or absence of liver metastases. The primary end point was overall survival (OS). LEAP-017 is registered at ClinicalTrials.gov (NCT04776148), and has completed recruitment.

Results: Between April 8, 2021, and December 21, 2021, 480 patients were randomly assigned to lenvatinib plus pembrolizumab (n = 241) or SOC (n = 239). At final analysis (median follow-up of 18.6 months [IQR, 3.9]), median OS with lenvatinib plus pembrolizumab versus SOC was 9.8 versus 9.3 months (hazard ratio [HR], 0.83 [95% CI, 0.68 to 1.02]; P = .0379; prespecified threshold P = .0214). Grade ≥3 treatment-related adverse events occurred in 58.4% (lenvatinib plus pembrolizumab) versus 42.1% (SOC) of patients. Two participants died due to treatment-related adverse events, both in the lenvatinib plus pembrolizumab arm.

Conclusion: In patients with pMMR or not MSI-H mCRC that had progressed on previous therapy, there was no statistically significant improvement in OS after lenvatinib plus pembrolizumab treatment versus SOC. No new safety signals were observed.

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伦伐替尼联合 Pembrolizumab 与标准疗法治疗既往治疗过的转移性结直肠癌的对比:随机、开放标签、III 期 LEAP-017 研究的最终分析。
目的:对于既往接受过治疗的转移性结直肠癌(mCRC)患者来说,治疗方案非常有限。在LEAP-017研究中,我们评估了与标准治疗(SOC)相比,来伐替尼联合pembrolizumab是否能改善既往治疗过的错配修复熟练或非微卫星不稳定性高(pMMR或非MSI-H)mCRC的治疗效果:在这项国际多中心随机对照开放标签III期研究中,年龄在18岁及以上、不可切除、pMMR或非MSI-H型mCRC患者,经标准治疗后病情进展或不能耐受标准治疗者,按1:1比例随机分配到仑伐替尼20毫克口服,每日1次加pembrolizumab 400毫克静脉注射,每6周1次,或由研究者选择瑞戈非尼或三氟啶/替吡拉西(SOC)。随机化按是否存在肝转移进行分层。主要终点是总生存期(OS)。LEAP-017已在ClinicalTrials.gov(NCT04776148)上注册,并已完成招募:2021年4月8日至2021年12月21日期间,480名患者被随机分配到来伐替尼加pembrolizumab(n = 241)或SOC(n = 239)。在最终分析中(中位随访18.6个月[IQR,3.9]),来伐替尼联合pembrolizumab与SOC的中位OS分别为9.8个月和9.3个月(危险比[HR],0.83[95% CI,0.68至1.02];P = .0379;预设阈值P = .0214)。58.4%(来伐替尼加pembrolizumab)和42.1%(SOC)的患者发生了≥3级治疗相关不良事件。两名参与者死于治疗相关不良事件,均为来伐替尼加pembrolizumab治疗组:结论:对于既往治疗进展的pMMR或非MSI-H型mCRC患者,与SOC相比,来伐替尼联合pembrolizumab治疗后的OS没有统计学意义上的显著改善。未观察到新的安全性信号。
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
Journal of Clinical Oncology
Journal of Clinical Oncology 医学-肿瘤学
CiteScore
41.20
自引率
2.20%
发文量
8215
审稿时长
2 months
期刊介绍: The Journal of Clinical Oncology serves its readers as the single most credible, authoritative resource for disseminating significant clinical oncology research. In print and in electronic format, JCO strives to publish the highest quality articles dedicated to clinical research. Original Reports remain the focus of JCO, but this scientific communication is enhanced by appropriately selected Editorials, Commentaries, Reviews, and other work that relate to the care of patients with cancer.
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