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Event-free Survival with Pembrolizumab in Early Triple-Negative Breast Cancer

医学 彭布罗利珠单抗 乳腺癌 表阿霉素 内科学 安慰剂 新辅助治疗 肿瘤科 环磷酰胺 外科 三阴性乳腺癌 化疗 卡铂 中期分析
作者
Peter Schmid,Javier Cortés,Rebecca Dent,Lajos Pusztai,Heather McArthur,Sherko Kümmel,Jonas Bergh,Carsten Denkert,Yeon Hee Park,Rina Hui,Nadia Harbeck,Masato Takahashi,Michael Untch,Peter A. Fasching,Fatima Cardoso,Jay Andersen,Debra Patt,Michael Danso,Marta Ferreira,Marie-Ange Mouret-Reynier,Seock-Ah Im,Jin-Hee Ahn,Maria Gion,Sally Baron-Hay,Jean-François Boileau,Yu Ding,Konstantinos Tryfonidis,Gursel Aktan,Vassiliki Karantza,Joyce O’Shaughnessy
出处
期刊:The New England Journal of Medicine [Massachusetts Medical Society]
卷期号:386 (6): 556-567 被引量:22
标识
DOI:10.1056/nejmoa2112651
摘要

The addition of pembrolizumab to neoadjuvant chemotherapy led to a significantly higher percentage of patients with early triple-negative breast cancer having a pathological complete response (defined as no invasive cancer in the breast and negative nodes) at definitive surgery in an earlier analysis of this phase 3 trial of neoadjuvant and adjuvant therapy. The primary results regarding event-free survival in this trial have not been reported.We randomly assigned, in a 2:1 ratio, patients with previously untreated stage II or III triple-negative breast cancer to receive neoadjuvant therapy with four cycles of pembrolizumab (at a dose of 200 mg) or placebo every 3 weeks plus paclitaxel and carboplatin, followed by four cycles of pembrolizumab or placebo plus doxorubicin-cyclophosphamide or epirubicin-cyclophosphamide. After definitive surgery, patients received adjuvant pembrolizumab (pembrolizumab-chemotherapy group) or placebo (placebo-chemotherapy group) every 3 weeks for up to nine cycles. The primary end points were pathological complete response (the results for which have been reported previously) and event-free survival, defined as the time from randomization to the date of disease progression that precluded definitive surgery, local or distant recurrence, occurrence of a second primary cancer, or death from any cause. Safety was also assessed.Of the 1174 patients who underwent randomization, 784 were assigned to the pembrolizumab-chemotherapy group and 390 to the placebo-chemotherapy group. The median follow-up at this fourth planned interim analysis (data cutoff, March 23, 2021) was 39.1 months. The estimated event-free survival at 36 months was 84.5% (95% confidence interval [CI], 81.7 to 86.9) in the pembrolizumab-chemotherapy group, as compared with 76.8% (95% CI, 72.2 to 80.7) in the placebo-chemotherapy group (hazard ratio for event or death, 0.63; 95% CI, 0.48 to 0.82; P<0.001). Adverse events occurred predominantly during the neoadjuvant phase and were consistent with the established safety profiles of pembrolizumab and chemotherapy.In patients with early triple-negative breast cancer, neoadjuvant pembrolizumab plus chemotherapy, followed by adjuvant pembrolizumab after surgery, resulted in significantly longer event-free survival than neoadjuvant chemotherapy alone. (Funded by Merck Sharp and Dohme, a subsidiary of Merck; KEYNOTE-522 ClinicalTrials.gov number, NCT03036488.).
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