Pembrolizumab plus Abiraterone Acetate and Prednisone in Patients with Chemotherapy-naïve Metastatic Castration-resistant Prostate Cancer: Results from KEYNOTE-365 Cohort D.

IF 8.3 1区 医学 Q1 ONCOLOGY European urology oncology Pub Date : 2024-06-25 DOI:10.1016/j.euo.2024.05.013
Evan Y Yu, Cristiano Ferrario, Mark D Linch, Michael Stoeckle, Brigitte Laguerre, Jose A Arranz, Tilman Todenhöfer, Peter C Fong, Josep M Piulats, William Berry, Urban Emmenegger, Loic Mourey, Anthony M Joshua, Nataliya Mar, Leonard J Appleman, Henry J Conter, Gwenaelle Gravis, Xin Tong Li, Charles Schloss, Christian Poehlein, Johann S de Bono
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Abstract

Background and objective: Abiraterone acetate (abiraterone) plus prednisone is approved for the treatment of metastatic castration-resistant prostate cancer (mCRPC). Our aim was to evaluate the efficacy and safety of pembrolizumab plus abiraterone in mCRPC.

Methods: In cohort D of the phase 1b/2 KEYNOTE-365 study (NCT02861573), patients were chemotherapy-naïve, had disease progression ≤6 mo before screening, and had either not received prior next-generation hormonal agents for mCRPC or had received prior enzalutamide for mCRPC and had disease progression or became intolerant to enzalutamide. Patients received pembrolizumab 200 mg intravenously every 3 wk plus abiraterone 1000 mg orally once daily and prednisone 5 mg orally twice daily. The primary endpoints were safety, prostate-specific antigen (PSA) response rate, and objective response rate (ORR) according to Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1) by blinded independent central review (BICR). Secondary endpoints included radiographic progression-free survival (rPFS) according to Prostate Cancer Clinical Trials Working Group 3-modified RECIST v1.1 by BICR and overall survival (OS).

Key findings and limitations: For the 103 patients who were treated, median follow-up was 28 mo (interquartile range 26-31). The confirmed PSA response rate was 56% (58/103 patients). The ORR for patients with RECIST v1.1-measurable disease was 16% (6/37 patients). Median rPFS was 15 mo (95% confidence interval 9.2-22) and median OS was 30 mo (95% confidence interval 23-not reached); the estimated 24-mo OS rate was 58%. In total, 91% of patients experienced treatment-related adverse events, and 39% experienced grade 3-5 events. Grade 3/4 elevation of alanine aminotransferase (ALT) or aspartate aminotransferase (AST) was observed in 12% and 6.8% of patients, respectively. One patient died due to treatment-related myasthenic syndrome. Study limitations include the single-arm design.

Conclusions: Pembrolizumab plus abiraterone and prednisone demonstrated antitumor activity and acceptable safety in patients with chemotherapy-naïve mCRPC. Higher incidence of grade 3/4 elevated ALT/AST occurred than was reported for the individual agents.

Patient summary: For patients with metastatic castratation-resistant prostate cancer, the drug combination of pembrolizumab plus abiraterone and prednisone showed antitumor activity and acceptable safety.

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Pembrolizumab联合醋酸阿比特龙和泼尼松治疗化疗无效的转移性抗阉割前列腺癌患者:KEYNOTE-365队列D的研究结果。
背景和目的:醋酸阿比特龙(abiraterone acetate)加泼尼松已被批准用于治疗转移性抗性前列腺癌(mCRPC)。我们的目的是评估pembrolizumab加阿比特龙治疗mCRPC的疗效和安全性:在1b/2期KEYNOTE-365研究(NCT02861573)的队列D中,患者均为化疗无效患者,筛选前疾病进展≤6个月,既往未接受过新一代激素药物治疗mCRPC,或既往接受过恩杂鲁胺治疗mCRPC,但疾病进展或对恩杂鲁胺不耐受。患者每3周静脉注射200毫克pembrolizumab,同时口服阿比特龙1000毫克,每天1次;口服泼尼松5毫克,每天2次。主要终点是安全性、前列腺特异性抗原(PSA)反应率,以及根据实体瘤反应评估标准1.1版(RECIST v1.1)通过盲法独立中央审查(BICR)得出的客观反应率(ORR)。次要终点包括BICR根据前列腺癌临床试验工作组3修订版RECIST v1.1得出的放射学无进展生存期(rPFS)和总生存期(OS):在接受治疗的103名患者中,中位随访时间为28个月(四分位间范围为26-31)。经证实的 PSA 反应率为 56%(58/103 例患者)。RECIST v1.1-可测量疾病患者的ORR为16%(6/37例)。中位 RPFS 为 15 个月(95% 置信区间为 9.2-22),中位 OS 为 30 个月(95% 置信区间为 23-未达到);估计 24 个月的 OS 率为 58%。91%的患者出现了治疗相关不良事件,其中39%的患者出现了3-5级不良事件。分别有12%和6.8%的患者出现3/4级丙氨酸氨基转移酶(ALT)或天冬氨酸氨基转移酶(AST)升高。一名患者死于与治疗相关的肌无力综合征。研究的局限性包括单臂设计:Pembrolizumab联合阿比特龙和泼尼松对化疗无效的mCRPC患者具有抗肿瘤活性和可接受的安全性。3/4级ALT/AST升高的发生率高于个别药物:对于转移性阉割耐药前列腺癌患者,pembrolizumab加阿比特龙和泼尼松的联合用药显示出抗肿瘤活性和可接受的安全性。
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来源期刊
CiteScore
15.50
自引率
2.40%
发文量
128
审稿时长
20 days
期刊介绍: Journal Name: European Urology Oncology Affiliation: Official Journal of the European Association of Urology Focus: First official publication of the EAU fully devoted to the study of genitourinary malignancies Aims to deliver high-quality research Content: Includes original articles, opinion piece editorials, and invited reviews Covers clinical, basic, and translational research Publication Frequency: Six times a year in electronic format
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