PD-L1 Expression in Biliary Tract Cancer: Comparison Across Antibody Clones and Role as a Predictor of Response to Chemoimmunotherapy: A Meta-Analysis.

IF 5.3 2区 医学 Q1 ONCOLOGY
JCO precision oncology Pub Date : 2025-05-01 Epub Date: 2025-05-29 DOI:10.1200/PO-24-00475
Juan J Juarez-Vignon Whaley, Soravis Osataphan, Ben Ponvilawan, Nipith Charoenngam, Mary Linton Peters
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Abstract

Purpose: PD-L1 positivity in biliary tract cancers (BTCs) is reported from 4% to 76%. BTC clinical trials have not demonstrated PD-L1 expression as a predictor of response to chemotherapy combined with immune checkpoint inhibitor (chemo-ICI). This meta-analysis examines PD-L1 positivity rates in BTC and association between PD-L1 expression and outcomes in patients treated with chemo-ICI.

Materials and methods: Observational studies or clinical trials reporting tissue-based PD-L1 expression by Tumor Proportional Score/Combined Positive Score using immunohistochemistry were included. Clinical trials of BTC treated with chemo-ICI were included to assess PD-L1 expression on treatment response. PubMed, Embase, Web of Science, and Cochrane Library were searched for relevant studies before November 15, 2023. Methods of PD-L1 assessment, including antibody clone, cutoff for PD-L1 positivity, and anatomical subtype, were analyzed. Overall survival (OS) and objective response rates (ORRs) were the main outcomes. The generic inverse variance method and random-effect model were used to assess pooled effect sizes.

Results: Fifty-six studies met eligibility criteria. Among 7,768 patients, pooled PD-L1 positivity was 30%. Positivity rates varied significantly by antibody clone (5H1, 58% v SP142, 17%; P = .02). Clinical trials reported a higher positivity rate compared with observational studies (48% v 26%; P < .01). Across five phase I/II clinical trials (194 patients), PD-L1 ≥1% patients tended to have a better ORR than PD-L1 <1% patients (64% v 46%; P = .08). In two randomized controlled trials (874 patients), PD-L1 ≥1% had a statistically significant improvement in OS (hazard ratio [HR], 0.83; P < .01), while PD-L1 <1% did not (HR, 0.85; P = .2).

Conclusion: Given the high PD-L1 positivity rate seen in this study, as well as a possible signal of predictive response for chemo-ICI treatment, PD-L1 expression should be further explored as a predictive biomarker.

胆道癌中PD-L1的表达:抗体克隆的比较和作为化疗免疫治疗反应预测因子的作用:一项meta分析
目的:胆道肿瘤(btc)中PD-L1阳性从4%上升到76%。BTC临床试验尚未证明PD-L1表达是化疗联合免疫检查点抑制剂(chemo-ICI)应答的预测因子。本荟萃分析探讨了化疗ici患者BTC中PD-L1的阳性率以及PD-L1表达与预后之间的关系。材料和方法:纳入观察性研究或临床试验,通过肿瘤比例评分/免疫组织化学联合阳性评分报告组织基础PD-L1表达。采用化学- ici治疗BTC的临床试验,评估PD-L1表达对治疗反应的影响。检索PubMed、Embase、Web of Science和Cochrane Library在2023年11月15日前的相关研究。分析PD-L1的评估方法,包括抗体克隆、PD-L1阳性切断和解剖亚型。总生存期(OS)和客观缓解率(orr)是主要结局。采用通用反方差法和随机效应模型评估合并效应大小。结果:56项研究符合入选标准。在7768例患者中,PD-L1总阳性率为30%。不同抗体克隆的阳性率差异显著(5H1, 58% vs SP142, 17%;P = .02)。与观察性研究相比,临床试验报告的阳性率更高(48% vs 26%;P < 0.01)。在5个I/II期临床试验(194例患者)中,PD-L1≥1%的患者往往比PD-L1≥46%的患者有更好的ORR;P = .08)。在两项随机对照试验(874例患者)中,PD-L1≥1%的患者OS改善具有统计学意义(风险比[HR], 0.83;P < 0.01), PD-L1 P = 0.2)。结论:考虑到本研究中PD-L1的高阳性率,以及对化学- ici治疗的预测反应的可能信号,PD-L1表达应进一步探索作为预测生物标志物。
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
CiteScore
9.10
自引率
4.30%
发文量
363
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