Pembrolizumab as Second-Line Therapy for Advanced Urothelial Carcinoma

被引:2727
作者
Bellmunt, J. [1 ,2 ]
de Wit, R. [4 ]
Vaughn, D. J. [6 ]
Fradet, Y. [7 ]
Lee, J. -L. [8 ,9 ]
Fong, L. [10 ]
Vogelzang, N. J. [11 ]
Climent, M. A. [3 ]
Petrylak, D. P. [12 ]
Choueiri, T. K. [1 ]
Necchi, A. [13 ]
Gerritsen, W. [5 ]
Gurney, H. [14 ,15 ]
Quinn, D. I. [16 ]
Culine, S. [17 ]
Sternberg, C. N. [18 ,19 ]
Mai, Y. [20 ]
Poehlein, C. H. [20 ]
Perini, R. F. [20 ]
Bajorin, D. F. [21 ]
机构
[1] Dana Farber Canc Inst, 450 Brookline Ave,Dana Bldg 1230, Boston, MA 02215 USA
[2] Hosp Mar, Med Res Inst, Parc Salut Mar, Barcelona, Spain
[3] Fdn Inst Valenciano Oncol, Valencia, Spain
[4] Erasmus MC Canc Inst, Rotterdam, Netherlands
[5] Radboud Univ Nijmegen, Med Ctr, Nijmegen, Netherlands
[6] Univ Penn, Abramson Canc Ctr, Philadelphia, PA 19104 USA
[7] Univ Laval, Ctr Hosp Univ Quebec, Quebec City, PQ, Canada
[8] Asan Med Ctr, Seoul, South Korea
[9] Univ Ulsan, Coll Med, Seoul, South Korea
[10] Univ Calif San Francisco, San Francisco, CA 94143 USA
[11] Comprehens Canc Ctr Nevada, Las Vegas, NV USA
[12] Yale Univ, Smilow Canc Hosp, New Haven, CT USA
[13] Fdn IRCCS Ist Nazl Tumori, Milan, Italy
[14] Westmead Hosp, Sydney, NSW, Australia
[15] Macquarie Univ, Sydney, NSW, Australia
[16] Univ Southern Calif, Norris Comprehens Canc Ctr & Hosp, Los Angeles, CA USA
[17] Hop St Louis, Paris, France
[18] San Camillo Hosp, Rome, Italy
[19] Forlanini Hosp, Rome, Italy
[20] Merck, Kenilworth, NJ USA
[21] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
关键词
TRANSITIONAL-CELL CARCINOMA; PHASE-III TRIAL; VINFLUNINE PLUS; SUPPORTIVE CARE; NIVOLUMAB; CHEMOTHERAPY; FAILURE; CANCER;
D O I
10.1056/NEJMoa1613683
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Patients with advanced urothelial carcinoma that progresses after platinum-based chemotherapy have a poor prognosis and limited treatment options. METHODS In this open-label, international, phase 3 trial, we randomly assigned 542 patients with advanced urothelial cancer that recurred or progressed after platinum-based chemotherapy to receive pembrolizumab (a highly selective, humanized monoclonal IgG kappa. isotype antibody against programmed death 1 [PD-1]) at a dose of 200 mg every 3 weeks or the investigator's choice of chemotherapy with paclitaxel, docetaxel, or vinflunine. The coprimary end points were overall survival and progression-free survival, which were assessed among all patients and among patients who had a tumor PD-1 ligand (PD-L1) combined positive score (the percentage of PD-L1-expressing tumor and infiltrating immune cells relative to the total number of tumor cells) of 10% or more. RESULTS The median overall survival in the total population was 10.3 months (95% confidence interval [CI], 8.0 to 11.8) in the pembrolizumab group, as compared with 7.4 months (95% CI, 6.1 to 8.3) in the chemotherapy group (hazard ratio for death, 0.73; 95% CI, 0.59 to 0.91; P = 0.002). The median overall survival among patients who had a tumor PD-L1 combined positive score of 10% or more was 8.0 months (95% CI, 5.0 to 12.3) in the pembrolizumab group, as compared with 5.2 months (95% CI, 4.0 to 7.4) in the chemotherapy group (hazard ratio, 0.57; 95% CI, 0.37 to 0.88; P = 0.005). There was no significant between-group difference in the duration of progression-free survival in the total population (hazard ratio for death or disease progression, 0.98; 95% CI, 0.81 to 1.19; P = 0.42) or among patients who had a tumor PD-L1 combined positive score of 10% or more (hazard ratio, 0.89; 95% CI, 0.61 to 1.28; P = 0.24). Fewer treatment-related adverse events of any grade were reported in the pembrolizumab group than in the chemotherapy group (60.9% vs. 90.2%); there were also fewer events of grade 3, 4, or 5 severity reported in the pembrolizumab group than in the chemotherapy group (15.0% vs. 49.4%). CONCLUSIONS Pembrolizumab was associated with significantly longer overall survival (by approximately 3 months) and with a lower rate of treatment-related adverse events than chemotherapy as second-line therapy for platinum-refractory advanced urothelial carcinoma.Funded by Merck; KEYNOTE- 045 ClinicalTrials. gov number, NCT02256436.)
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页码:1015 / 1026
页数:12
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