Pembrolizumab in Patients With Advanced Triple-Negative Breast Cancer: Phase Ib KEYNOTE-012 Study

被引:877
作者
Nanda, Rita [1 ]
Chow, Laura Q. M. [2 ]
Dees, E. Claire [3 ]
Berger, Raanan [4 ]
Gupta, Shilpa [6 ]
Geva, Ravit [5 ]
Pusztai, Lajos [7 ]
Pathiraja, Kumudu [8 ]
Aktan, Gursel [8 ]
Cheng, Jonathan D. [8 ]
Karantza, Vassiliki [8 ]
Buisseret, Laurence [9 ]
机构
[1] Univ Chicago, 5481 S Maryland Ave,MC 2115, Chicago, IL 60637 USA
[2] Univ Washington, Seattle, WA 98195 USA
[3] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[4] Sheba Med Ctr, Tel Hashomer, Israel
[5] Tel Aviv Sourasky Med Ctr, Tel Aviv, Israel
[6] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[7] Yale Univ, Sch Med, New Haven, CT USA
[8] Merck & Co Inc, Kenilworth, NJ USA
[9] Univ Libre Bruxelles, Brussels, Belgium
关键词
TUMOR-INFILTRATING LYMPHOCYTES; REGULATORY T-CELLS; MOLECULAR SUBTYPES; PD-L1; EXPRESSION; PROGNOSTIC VALUE; BASAL; CHEMOTHERAPY; METASTASIS; MUTATIONS; PROTEIN;
D O I
10.1200/JCO.2015.64.8931
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
Purpose Immune checkpoint inhibition has been demonstrated to be an effective anticancer strategy. Several lines of evidence support the study of immunotherapy in triple-negative breast cancer (TNBC). We assessed the safety and antitumor activity of the programmed cell death protein 1 (PD-1) inhibitor pembrolizumab in patients with advanced TNBC. Methods KEYNOTE-012 (ClinicalTrials.gov identifier: NCT01848834) was a multicenter, nonrandomized phase Ib trial of single-agent pembrolizumab given intravenously at 10 mg/kg every 2 weeks to patients with advanced PD-L1-positive (expression in stroma or 1% of tumor cells by immunohistochemistry) TNBC, gastric cancer, urothelial cancer, and head and neck cancer. This report focuses on the TNBC cohort. Results Among 111 patients with TNBC whose tumor samples were screened for PD-L1 expression, 58.6% had PD-L1-positive tumors. Thirty-two women (median age, 50.5 years; range, 29 to 72 years) were enrolled and assessed for safety and antitumor activity. The median number of doses administered was five (range, 1 to 36 doses). Common toxicities were mild and similar to those observed in other tumor cohorts (eg, arthralgia, fatigue, myalgia, and nausea), and included five (15.6%) patients with grade 3 toxicity and one treatment-related death. Among the 27 patients who were evaluable for antitumor activity, the overall response rate was 18.5%, the median time to response was 17.9 weeks (range, 7.3 to 32.4 weeks), and the median duration of response was not yet reached (range, 15.0 to 47.3 weeks). Conclusion This phase Ib study describes preliminary evidence of clinical activity and a potentially acceptable safety profile of pembrolizumab given every 2 weeks to patients with heavily pretreated, advanced TNBC. A single-agent phase II study examining a 200-mg dose given once every 3 weeks (ClinicalTrials.gov identifier: NCT02447003) is ongoing. (C) 2016 by American Society of Clinical Oncology
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收藏
页码:2460 / +
页数:10
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