揭示基于免疫检查点抑制剂的一线转移性肾细胞癌最佳治疗方案:最新的系统综述和贝叶斯网络分析

IF 4.2 2区 医学 Q2 ONCOLOGY
Therapeutic Advances in Medical Oncology Pub Date : 2025-07-06 eCollection Date: 2025-01-01 DOI:10.1177/17588359251353259
Junpeng Wang, Xin Li, Mengjun Li, Qingyuan Liu, Zixuan Xie, Xiaotian Si, Lei Yang, Zhifeng Wang, Degang Ding
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引用次数: 0

摘要

背景:基于免疫检查点抑制剂(ICI)的联合治疗已被推荐为转移性肾细胞癌(mRCC)的一线治疗方案;然而,没有随机对照试验(rct)比较所有现有的基于ici的治疗。目的:我们旨在分析最新数据,比较所有可用的基于ci的mRCC方案的疗效。设计:系统回顾和贝叶斯网络分析。数据来源和方法:系统检索截至2024年9月15日的文献,后续采用贝叶斯固定效应模型进行分析。结果:本研究纳入30项随机对照试验,涉及14959例患者。结果显示,纳武单抗联合卡博赞替尼(风险比(HR): 0.77;95%可信区间(CrI): 0.63-0.93),派姆单抗联合lenvatinib (HR: 0.79;95% CrI: 0.64-0.99),托帕利单抗+阿西替尼(HR: 0.62;95% CrI: 0.42-0.97),纳武单抗联合伊匹单抗(HR: 0.72;95% CrI: 0.62-0.84),派姆单抗联合阿西替尼(HR: 0.84;95% CrI: 0.71-0.98),阿维单抗联合阿西替尼(HR: 0.79;95% CrI: 0.64-0.98)在总生存期(OS)方面显著优于舒尼替尼。除了派姆单抗和lenvatinib外,大多数基于ci的联合治疗与舒尼替尼相比导致更少或相似的高级不良事件。对于有利风险患者,基于ici的联合疗法在OS方面并不比舒尼替尼更有效,而对于中危或低危患者,有6种基于ici的联合疗法与舒尼替尼相比显着改善OS相关。结论:我们的研究结果表明,包括尼武单抗加卡博赞替尼、派姆单抗加lenvatinib、托利帕单抗加阿西替尼、尼武单抗加伊匹单抗、派姆单抗加阿西替尼和avelumab加阿西替尼在内的联合治疗相比舒尼替尼显著改善了OS。在亚组分析中,基于ci的联合治疗在中危或低危患者中表现出明显优于舒尼替尼的优势,而这种优势在治疗有利危患者中减弱。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Unveiling the best immune checkpoint inhibitor-based therapy for metastatic renal cell carcinoma in the first-line setting: an updated systematic review and Bayesian network analysis.

Unveiling the best immune checkpoint inhibitor-based therapy for metastatic renal cell carcinoma in the first-line setting: an updated systematic review and Bayesian network analysis.

Unveiling the best immune checkpoint inhibitor-based therapy for metastatic renal cell carcinoma in the first-line setting: an updated systematic review and Bayesian network analysis.

Unveiling the best immune checkpoint inhibitor-based therapy for metastatic renal cell carcinoma in the first-line setting: an updated systematic review and Bayesian network analysis.

Background: Immune checkpoint inhibitor (ICI)-based combination therapies have been recommended as first-line options for metastatic renal cell carcinoma (mRCC); however, no head-to-head randomized controlled trials (RCTs) have compared all existing ICI-based therapies.

Objective: We aimed to analyze the updated data to compare the efficacy of all available ICI-based options for mRCC.

Design: A systematic review and Bayesian network analysis.

Data sources and methods: A systematic literature search was undertaken up to September 15, 2024, and subsequent analysis was performed using a Bayesian fixed-effect model.

Results: This study included 30 RCTs involving 14,959 patients. The results revealed that nivolumab plus cabozantinib (hazard ratio (HR): 0.77; 95% credible interval (CrI): 0.63-0.93), pembrolizumab plus lenvatinib (HR: 0.79; 95% CrI: 0.64-0.99), toripalimab plus axitinib (HR: 0.62; 95% CrI: 0.42-0.97), nivolumab plus ipilimumab (HR: 0.72; 95% CrI: 0.62-0.84), pembrolizumab plus axitinib (HR: 0.84; 95% CrI: 0.71-0.98), and avelumab plus axitinib (HR: 0.79; 95% CrI: 0.64-0.98) were significantly more effective than sunitinib for overall survival (OS). Most ICI-based combination treatments resulted in fewer or similar high-grade adverse events compared to sunitinib, except for pembrolizumab plus lenvatinib. For favorable-risk patients, ICI-based combination therapies were not more effective than sunitinib in OS, while six ICI-based combination therapies were associated with significantly improved OS compared to sunitinib for intermediate-risk or poor-risk patients.

Conclusion: Our findings demonstrated that combination therapies including nivolumab plus cabozantinib, pembrolizumab plus lenvatinib, toripalimab plus axitinib, nivolumab plus ipilimumab, pembrolizumab plus axitinib, and avelumab plus axitinib significantly improved OS versus sunitinib. For subgroup analysis, ICI-based combination therapies exhibited significant advantages over sunitinib for intermediate-risk or poor-risk patients, while such advantages were diminished in treating favorable-risk patients.

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来源期刊
CiteScore
8.20
自引率
2.00%
发文量
160
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Medical Oncology is an open access, peer-reviewed journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of cancer. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in medical oncology, providing a forum in print and online for publishing the highest quality articles in this area. This journal is a member of the Committee on Publication Ethics (COPE).
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