Pembrolizumab plus chemotherapy in advanced or recurrent endometrial cancer: overall survival and exploratory analyses of the NRG GY018 phase 3 randomized trial

IF 50 1区 医学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY Nature Medicine Pub Date : 2025-03-05 DOI:10.1038/s41591-025-03566-1
Ramez N. Eskander, Michael W. Sill, Lindsey Beffa, Richard G. Moore, Joanie M. Hope, Fernanda B. Musa, Robert S. Mannel, Mark S. Shahin, Guilherme H. Cantuaria, Eugenia Girda, Elizabeth Lokich, Juraj Kavecansky, Charles A. Leath III, Lilian T. Gien, Emily M. Hinchcliff, Shashikant B. Lele, Lisa M. Landrum, Floor Backes, Roisin E. O’Cearbhaill, Tareq Al Baghdadi, Emily K. Hill, Premal H. Thaker, Veena S. John, Stephen Welch, Amanda N. Fader, Matthew A. Powell, Carol Aghajanian
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Abstract

Historically, the treatment of patients with advanced stage or recurrent endometrial cancer included paclitaxel plus carboplatin. Immunotherapy in combination with chemotherapy resulted in improved clinical outcomes in several solid tumors. In the phase 3 NRG GY018 study, pembrolizumab plus chemotherapy significantly improved investigator-assessed progression-free survival (PFS; primary endpoint) versus placebo plus chemotherapy in patients with advanced/metastatic/recurrent endometrial cancer regardless of mismatch repair status. Here we report on key secondary endpoints and exploratory analyses. Patients were women ≥18 years old with newly diagnosed stage III or IVA endometrial cancer with measurable disease, or stage IVB or recurrent endometrial cancer with or without measurable disease. Patients (n = 810) were randomized (1:1) to pembrolizumab or placebo plus paclitaxel–carboplatin followed by maintenance pembrolizumab or placebo for up to 24 months. Overall survival was a secondary endpoint and PFS per RECIST v.1.1 by blinded independent central review was an exploratory endpoint. Overall survival data were immature; hazard ratios favored pembrolizumab (mismatch repair-proficient: 0.79 (0.53–1.17); 1-sided nominal P = 0.1157; mismatch repair-deficient: 0.55 (0.25–1.19); 1-sided nominal P = 0.0617). Hazard ratios (95% confidence intervals) for PFS per blinded independent central review favored pembrolizumab (mismatch repair-proficient: 0.64 (0.49–0.85); P = 0.0008; mismatch repair-deficient: 0.45 (0.27–0.73); P = 0.0005). These findings further support the use of pembrolizumab plus chemotherapy as first-line treatment for patients with advanced stage or recurrent endometrial cancer regardless of mismatch repair status. ClinicalTrials.gov identifier: NCT03914612 . Secondary and exploratory analyses of the phase 3 NRG GY018 trial show that, in patients with advanced or recurrent endometrial cancer, first-line treatment with pembrolizumab together with paclitaxel and carboplatin leads to prolonged progression-free survival, according to blinded independent central review.

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Pembrolizumab联合化疗治疗晚期或复发性子宫内膜癌:NRG GY018 3期随机试验的总生存期和探索性分析
历史上,晚期或复发子宫内膜癌患者的治疗包括紫杉醇加卡铂。免疫治疗联合化疗可改善几种实体瘤的临床预后。在NRG GY018的3期研究中,派姆单抗加化疗显著改善了研究者评估的无进展生存期(PFS;无论错配修复状态如何,晚期/转移性/复发子宫内膜癌患者与安慰剂加化疗的对比。在这里,我们报告了关键的次要终点和探索性分析。患者为≥18岁的女性,新诊断的III期或IVA期子宫内膜癌伴可测量疾病,或IVB期或复发子宫内膜癌伴或不伴可测量疾病。810名患者(n = 810)随机(1:1)接受派姆单抗或安慰剂加紫杉醇卡铂治疗,随后再接受维持派姆单抗或安慰剂治疗长达24个月。总生存期是次要终点,根据RECIST v.1.1进行的盲法独立中心评价的PFS是一个探索性终点。总体生存数据不成熟;风险比倾向于派姆单抗(错配修复精通:0.79 (0.53-1.17);单侧名义P = 0.1157;错配修复缺陷:0.55 (0.25-1.19);单侧名义P = 0.0617)。根据盲法独立中心评价,PFS的风险比(95%置信区间)倾向于派姆单抗(错配修复精通:0.64 (0.49-0.85);p = 0.0008;错配修复缺陷:0.45 (0.27-0.73);p = 0.0005)。这些发现进一步支持使用派姆单抗联合化疗作为晚期或复发性子宫内膜癌患者的一线治疗,无论错配修复状态如何。ClinicalTrials.gov识别码:NCT03914612。
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来源期刊
Nature Medicine
Nature Medicine 医学-生化与分子生物学
CiteScore
100.90
自引率
0.70%
发文量
525
审稿时长
1 months
期刊介绍: Nature Medicine is a monthly journal publishing original peer-reviewed research in all areas of medicine. The publication focuses on originality, timeliness, interdisciplinary interest, and the impact on improving human health. In addition to research articles, Nature Medicine also publishes commissioned content such as News, Reviews, and Perspectives. This content aims to provide context for the latest advances in translational and clinical research, reaching a wide audience of M.D. and Ph.D. readers. All editorial decisions for the journal are made by a team of full-time professional editors. Nature Medicine consider all types of clinical research, including: -Case-reports and small case series -Clinical trials, whether phase 1, 2, 3 or 4 -Observational studies -Meta-analyses -Biomarker studies -Public and global health studies Nature Medicine is also committed to facilitating communication between translational and clinical researchers. As such, we consider “hybrid” studies with preclinical and translational findings reported alongside data from clinical studies.
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