Pembrolizumab Plus Docetaxel Versus Docetaxel for Previously Treated Metastatic Castration-Resistant Prostate Cancer: The Randomized, Double-Blind, Phase III KEYNOTE-921 Trial.

IF 42.1 1区 医学 Q1 ONCOLOGY
Journal of Clinical Oncology Pub Date : 2025-05-10 Epub Date: 2025-03-05 DOI:10.1200/JCO-24-01283
Daniel P Petrylak, Raffaele Ratta, Nobuaki Matsubara, Ernesto Korbenfeld, Rustem Gafanov, Loic Mourey, Tilman Todenhöfer, Howard Gurney, Gero Kramer, Andries M Bergman, Pawel Zalewski, Maria De Santis, Andrew J Armstrong, Winald Gerritsen, Russell Pachynski, Seok Soo Byun, Margitta Retz, Eric Levesque, Ray McDermott, Sergio Bracarda, Ray Manneh, Meital Levartovsky, Xin Tong Li, Charles Schloss, Christian H Poehlein, Karim Fizazi
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引用次数: 0

Abstract

Purpose: The standard of care for metastatic castration-resistant prostate cancer (mCRPC) after second-generation androgen receptor pathway inhibitor (ARPI) therapy is still docetaxel. The randomized, double-blind, phase III KEYNOTE-921 trial (Clinicaltrials.gov identifier: NCT03834506) evaluated the efficacy and safety of pembrolizumab or placebo plus docetaxel for previously treated mCRPC.

Methods: Adults with mCRPC who progressed after androgen-deprivation therapy and one ARPI were randomly assigned 1:1 to pembrolizumab or placebo plus docetaxel with concomitant prednisone. Dual primary end points were radiographic progression-free survival (rPFS) by blinded independent central review per Prostate Cancer Working Group 3-modified RECIST 1.1 and overall survival (OS). Safety was a secondary end point.

Results: Between May 30, 2019, and June 17, 2021, 515 participants were randomly assigned to pembrolizumab plus docetaxel and 515 to placebo plus docetaxel. Median time from random assignment to data cutoff date (June 20, 2022) at final analysis (FA) was 22.7 months (range, 12.1-36.7). At first interim analysis (data cutoff date: September 27, 2021), median rPFS was 8.6 months (95% CI, 8.3 to 10.2) with pembrolizumab plus docetaxel versus 8.3 months (95% CI, 8.2 to 8.5) with placebo plus docetaxel (hazard ratio [HR], 0.85 [95% CI, 0.71 to 1.01]; P = .03). At FA, median OS was 19.6 months (95% CI, 18.2 to 20.9) versus 19.0 months (95% CI, 17.9 to 20.9), respectively (HR, 0.92 [95% CI, 0.78 to 1.09]; P = .17). Grade ≥3 treatment-related adverse events occurred in 43.2% of participants who received pembrolizumab plus docetaxel and 36.6% of participants who received placebo plus docetaxel. Two and seven participants, respectively, died due to a treatment-related adverse event. Pneumonitis was the most common immune-mediated adverse event (7.0% v 3.1%).

Conclusion: The addition of pembrolizumab to docetaxel did not significantly improve efficacy outcomes for participants with previously treated mCRPC. The current standard of care remains unchanged.

Pembrolizumab联合多西他赛与多西他赛治疗转移性阉割抵抗性前列腺癌:随机,双盲,III期KEYNOTE-921试验
目的:转移性去势抵抗性前列腺癌(mCRPC)在第二代雄激素受体途径抑制剂(ARPI)治疗后的护理标准仍然是多西紫杉醇。这项随机、双盲、III期KEYNOTE-921试验(Clinicaltrials.gov标识号:NCT03834506)评估了派姆单抗或安慰剂加多西他赛治疗先前治疗过的mCRPC的疗效和安全性。方法:在雄激素剥夺治疗和一次ARPI治疗后进展的成年mCRPC患者随机按1:1分配到派姆单抗或安慰剂加多西他赛合并强的松组。双主要终点是根据前列腺癌工作组3-修订的RECIST 1.1进行的盲法独立中心评价的放射学无进展生存期(rPFS)和总生存期(OS)。安全性是次要的终点。结果:在2019年5月30日至2021年6月17日期间,515名参与者随机分配到派姆单抗+多西他赛组,515名参与者随机分配到安慰剂+多西他赛组。最终分析(FA)时,从随机分配到数据截止日期(2022年6月20日)的中位时间为22.7个月(范围12.1-36.7)。在首次中期分析中(数据截止日期:2021年9月27日),派姆单抗加多西他赛的中位rPFS为8.6个月(95% CI, 8.3至10.2),而安慰剂加多西他赛的中位rPFS为8.3个月(95% CI, 8.2至8.5)(风险比[HR], 0.85 [95% CI, 0.71至1.01];P = .03)。在FA时,中位OS分别为19.6个月(95% CI, 18.2至20.9)和19.0个月(95% CI, 17.9至20.9)(HR, 0.92 [95% CI, 0.78至1.09];P = .17)。43.2%接受派姆单抗加多西他赛的患者发生≥3级治疗相关不良事件,36.6%接受安慰剂加多西他赛的患者发生≥3级治疗相关不良事件。两名和七名参与者分别死于与治疗相关的不良事件。肺炎是最常见的免疫介导不良事件(7.0% vs 3.1%)。结论:在多西他赛的基础上添加派姆单抗并没有显著改善先前治疗过的mCRPC患者的疗效结果。目前的护理标准保持不变。
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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