Pembrolizumab plus Chemotherapy in Advanced Endometrial Cancer

被引:315
作者
Eskander, Ramez N. [1 ,2 ]
Sill, Michael W. [4 ]
Beffa, Lindsey [9 ]
Moore, Richard G. [5 ]
Hope, Joanie M. [12 ,13 ]
Musa, Fernanda B. [14 ]
Mannel, Robert [15 ]
Shahin, Mark S. [16 ]
Cantuaria, Guilherme H. [17 ]
Girda, Eugenia [18 ]
Mathews, Cara [19 ]
Kavecansky, Juraj [3 ]
Leath III, Charles A. [20 ]
Gien, Lilian T. [21 ]
Hinchcliff, Emily M. [23 ,24 ]
Lele, Shashikant B. [4 ]
Landrum, Lisa M. [25 ]
Backes, Floor [10 ,11 ]
O'Cearbhaill, Roisin E. [6 ,7 ]
Al Baghdadi, Tareq [26 ]
Hill, Emily K. [27 ]
Thaker, Premal H. [28 ]
John, Veena S. [8 ]
Welch, Stephen [22 ]
Fader, Amanda N. [29 ]
Powell, Matthew A. [28 ]
Aghajanian, Carol [6 ,7 ]
机构
[1] Univ Calif San Diego, Div Gynecol Oncol, Dept Obstet Gynecol & Reprod Sci, San Diego, CA USA
[2] Rebecca & John Moores Canc Ctr, La Jolla, CA USA
[3] Kaiser Permanente Natl Canc Inst Community Oncol, Antioch Med Ctr, Antioch, CA USA
[4] Roswell Pk Comprehens Canc, Clin Trial Dev Div, Dept Biostat & Bioinformat, Buffalo, NY USA
[5] Univ Rochester, Wilmot Canc Inst, Div Gynecol Oncol, Dept Obstet & Gynecol,Med Ctr, Rochester, NY USA
[6] Mem Sloan Kettering Canc Ctr, Dept Med, Gynecol Med Oncol Serv, New York, NY USA
[7] Weill Cornell Med Coll, Dept Med, New York, NY USA
[8] Northwell Hlth Canc Inst, New Hyde Pk, NY USA
[9] Cleveland Clin Fdn, Case Comprehens Canc Ctr, Cleveland, OH USA
[10] Ohio State Univ, Wexner Med Ctr, Columbus, OH USA
[11] James Canc Hosp, Columbus, OH USA
[12] Pacific Canc Res Consortium, NCORP, Alaska Womens Canc Care, Anchorage, AK USA
[13] Providence Alaska Canc Ctr, Anchorage, AK USA
[14] Pacific Canc Res Consortium, NCORP, Swedish Med Ctr Hill 1, Seattle, WA USA
[15] Univ Oklahoma, Hlth Sci Ctr, Oklahoma City, OK USA
[16] Jefferson Hlth, Asplundh Canc Pavil, Sidney Kimmel Canc Ctr, Jefferson Abington Hosp, Willow Grove, AR USA
[17] Georgia NCORP, Atlanta, GA USA
[18] Rutgers Canc Inst New Jersey, New Brunswick, NJ USA
[19] Brown Univ, Alpert Med Sch, Women & Infants Hosp, Legoretta Canc Ctr, Providence, RI USA
[20] Univ Alabama Birmingham, Deep South Res Consortium, ONeal Comprehens Canc Ctr, Univ Alabama Hosp, Birmingham, AL USA
[21] Sunnybrook Hlth Sci Ctr, Odette Canc Ctr, Toronto, ON, Canada
[22] London Reg Canc Program, London, ON, Canada
[23] Northwestern Univ, Feinberg Sch Med, Chicago, IL USA
[24] Northwestern Univ, Robert H Lurie Comprehens Canc Ctr, Chicago, IL USA
[25] Indiana Univ, Hlth Simon Canc Ctr, Indianapolis, IN USA
[26] Trinity Hlth IHA Med Grp, NCORP, Michigan Canc Res Consortium, Ypsilanti, MI USA
[27] Univ Iowa Hosp & Clin, Iowa City, IA USA
[28] Washington Univ, Div Gynecol Oncol, Dept Obstet & Gynecol, Sch Med, St Louis, MO USA
[29] Johns Hopkins Sch Med, Div Gynecol Oncol, Dept Gynecol & Obstet, Baltimore, MD USA
关键词
TUMORS;
D O I
10.1056/NEJMoa2302312
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Standard first-line chemotherapy for endometrial cancer is paclitaxel plus carboplatin. The benefit of adding pembrolizumab to chemotherapy remains unclear. METHODS In this double-blind, placebo-controlled, randomized, phase 3 trial, we assigned 816 patients with measurable disease (stage III or IVA) or stage IVB or recurrent endometrial cancer in a 1:1 ratio to receive pembrolizumab or placebo along with combination therapy with paclitaxel plus carboplatin. The administration of pembrolizumab or placebo was planned in 6 cycles every 3 weeks, followed by up to 14 maintenance cycles every 6 weeks. The patients were stratified into two cohorts according to whether they had mismatch repair-deficient (dMMR) or mismatch repair-proficient (pMMR) disease. Previous adjuvant chemotherapy was permitted if the treatment-free interval was at least 12 months. The primary outcome was progression-free survival in the two cohorts. Interim analyses were scheduled to be triggered after the occurrence of at least 84 events of death or progression in the dMMR cohort and at least 196 events in the pMMR cohort. RESULTS In the 12-month analysis, Kaplan-Meier estimates of progression-free survival in the dMMR cohort were 74% in the pembrolizumab group and 38% in the placebo group (hazard ratio for progression or death, 0.30; 95% confidence interval [CI], 0.19 to 0.48; P<0.001), a 70% difference in relative risk. In the pMMR cohort, median progression-free survival was 13.1 months with pembrolizumab and 8.7 months with placebo (hazard ratio, 0.54; 95% CI, 0.41 to 0.71; P<0.001). Adverse events were as expected for pembrolizumab and combination chemotherapy. CONCLUSIONS In patients with advanced or recurrent endometrial cancer, the addition of pembrolizumab to standard chemotherapy resulted in significantly longer progressionfree survival than with chemotherapy alone. (Funded by the National Cancer Institute and others; NRG-GY018 ClinicalTrials.gov number, NCT03914612.)
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页码:2159 / 2170
页数:12
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