Atezolizumab Combined With Platinum and Maintenance Niraparib for Recurrent Ovarian Cancer With a Platinum-Free Interval >6 Months: ENGOT-OV41/GEICO 69-O/ANITA Phase III Trial.

IF 42.1 1区 医学 Q1 ONCOLOGY Journal of Clinical Oncology Pub Date : 2024-12-20 Epub Date: 2024-09-18 DOI:10.1200/JCO.24.00668
Antonio González-Martín, María Jesús Rubio, Florian Heitz, René Depont Christensen, Nicoletta Colombo, Toon Van Gorp, Margarita Romeo, Isabelle Ray-Coquard, Lydia Gaba, Alexandra Leary, Luis Miguel De Sande, Coriolan Lebreton, Andrés Redondo, Michel Fabbro, Maria-Pilar Barretina Ginesta, Philippe Follana, J Alejandro Pérez-Fidalgo, Manuel Rodrigues, Ana Santaballa, Renaud Sabatier, Maria José Bermejo-Pérez, Jean-Pierre Lotz, Beatriz Pardo, Gloria Marquina, Luisa Sánchez-Lorenzo, María Quindós, Purificación Estévez-García, Eva Guerra Alía, Luis Manso, Victoria Casado, Stefan Kommoss, Germana Tognon, Stéphanie Henry, Ilan Bruchim, Ana Oaknin, Frédéric Selle
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引用次数: 0

Abstract

Purpose: To evaluate atezolizumab combined with platinum-based chemotherapy (CT) followed by maintenance niraparib for late-relapsing recurrent ovarian cancer.

Methods: The multicenter placebo-controlled double-blind randomized phase III ENGOT-OV41/GEICO 69-O/ANITA trial (ClinicalTrials.gov identifier: NCT03598270) enrolled patients with measurable high-grade serous, endometrioid, or undifferentiated recurrent ovarian cancer who had received one or two previous CT lines (most recent including platinum) and had a treatment-free interval since last platinum (TFIp) of >6 months. Patients were stratified by investigator-selected carboplatin doublet, TFIp, BRCA status, and PD-L1 status in de novo biopsy and randomly assigned 1:1 to receive either atezolizumab or placebo throughout standard therapy comprising six cycles of a carboplatin doublet followed (in patients with response/stable disease) by maintenance niraparib until progression. The primary end point was investigator-assessed progression-free survival (PFS) per RECIST v1.1.

Results: Between November 2018 and January 2022, 417 patients were randomly assigned (15% BRCA-mutated, 36% PD-L1-positive, 66% TFIp >12 months, 11% previous poly [ADP-ribose] polymerase inhibitor after frontline CT, and 53% previous bevacizumab). Median follow-up was 28.6 months (95% CI, 26.6 to 30.5 months). Atezolizumab did not significantly improve PFS (hazard ratio, 0.89 [95% CI, 0.71 to 1.10]; P = .28). Median PFS was 11.2 months (95% CI, 10.1 to 12.1 months) with atezolizumab versus 10.1 months (95% CI, 9.2 to 11.2 months) with standard therapy. Subgroup analyses generally showed consistent results, including analyses by PD-L1 status. The objective response rate (ORR) was 45% (95% CI, 39 to 52) with atezolizumab and 43% (95% CI, 36 to 49) with standard therapy. The safety profile was as expected from previous experience of these drugs.

Conclusion: Combining atezolizumab with CT and maintenance niraparib for late-relapsing recurrent ovarian cancer did not significantly improve PFS or the ORR.

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阿特珠单抗联合铂类和尼拉帕利治疗无铂期大于 6 个月的复发性卵巢癌:ENGOT-OV41/GEICO 69-O/ANITA III 期试验。
目的:评估阿特珠单抗联合铂类化疗(CT)和尼拉帕利维持治疗晚复发性卵巢癌的效果:多中心安慰剂对照双盲随机III期ENGOT-OV41/GEICO 69-O/ANITA试验(ClinicalTrials.gov标识符:NCT03598270)招募了可测量的高级别浆液性、子宫内膜样或未分化复发性卵巢癌患者,这些患者既往接受过一次或两次CT治疗(最近一次包括铂类药物),且自上次铂类药物治疗(TFIp)后无治疗间隔时间大于6个月。患者按研究者选择的卡铂双联疗法、TFIp、BRCA状态和新活检的PD-L1状态进行分层,并按1:1的比例随机分配接受阿特珠单抗或安慰剂治疗,整个标准治疗包括6个周期的卡铂双联疗法,然后(对有反应/病情稳定的患者)接受尼拉帕尼维持治疗,直至病情进展。主要终点是研究者评估的无进展生存期(PFS)(根据 RECIST v1.1.结果):2018年11月至2022年1月期间,417名患者被随机分配(15%为BRCA突变,36%为PD-L1阳性,66%为TFIp>12个月,11%在前线CT后曾使用过聚[ADP-核糖]聚合酶抑制剂,53%曾使用过贝伐单抗)。中位随访时间为 28.6 个月(95% CI,26.6 至 30.5 个月)。Atezolizumab并未显著改善PFS(危险比为0.89 [95% CI,0.71至1.10];P = .28)。阿特珠单抗的中位生存期为11.2个月(95% CI,10.1至12.1个月),而标准疗法的中位生存期为10.1个月(95% CI,9.2至11.2个月)。亚组分析结果基本一致,包括按PD-L1状态进行的分析。atezolizumab的客观反应率(ORR)为45%(95% CI,39-52),标准疗法为43%(95% CI,36-49)。根据以往使用这些药物的经验,安全性符合预期:结论:将atezolizumab与CT和维持性尼拉帕利联合治疗晚复发性卵巢癌并不能显著改善PFS或ORR。
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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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