Lenvatinib plus Pembrolizumab for Advanced Endometrial Cancer

被引:532
|
作者
Makker, V [1 ]
Colombo, N. [2 ]
Casado Herraez, A. [6 ]
Santin, A. D. [8 ]
Colomba, E. [9 ]
Miller, D. S. [11 ]
Fujiwara, K. [12 ]
Pignata, S. [3 ]
Baron-Hay, S. [16 ]
Ray-Coquard, I [10 ]
Shapira-Frommer, R. [17 ]
Ushijima, K. [13 ]
Sakata, J. [14 ]
Yonemori, K. [15 ]
Kim, Y. M. [18 ]
Guerra, E. M. [7 ]
Sanli, U. A. [19 ]
McCormack, M. M. [20 ]
Smith, A. D. [21 ]
Keefe, S. [22 ]
Bird, S. [22 ]
Dutta, L. [23 ]
Orlowski, R. J. [22 ]
Lorusso, D. [4 ,5 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Dept Med, Weill Cornell Med Ctr, St 5, New York, NY 10065 USA
[2] Univ Milano Bicocca, European Inst Oncol IRCCS, Milan, Italy
[3] Ist Nazl Tumori IRCCS Fdn G Pascale, Naples, Italy
[4] Fdn Policlin Univ Agostino Gemelli IRCCS, Rome, Italy
[5] Univ Cattolica Sacro Cuore, Rome, Italy
[6] San Carlos Univ Teaching Hosp, Madrid, Spain
[7] Hosp Univ Ramon y Cajal, Madrid, Spain
[8] Yale Univ, Sch Med, New Haven, CT USA
[9] Gustave Roussy Cancerol Inst, Grp Investigateurs Nationaux Etud Canc Ovariens G, Villejuif, France
[10] Univ Claude Bernard, Ctr Leon Berard, GLNECO, Lyon, France
[11] Univ Texas Southwestern Med Ctr Dallas, Dallas, TX 75390 USA
[12] Saitama Med Univ, Int Med Ctr, Hidaka, Japan
[13] Kurume Univ, Sch Med, Kurume, Fukuoka, Japan
[14] Aichi Canc Ctr Hosp, Nagoya, Aichi, Japan
[15] Natl Canc Ctr, Kokuritsu Gan Kenkyu Ctr Chuo Byoin, Tokyo, Japan
[16] Royal North Shore Hosp, St Leonards, NSW, Australia
[17] Sheba Med Ctr, Ramat Gan, Israel
[18] Univ Ulsan, Asan Med Ctr, Seoul, South Korea
[19] Ege Univ, Izmir, Turkey
[20] Univ Coll London Hosp NHS Fdn Trust, London, England
[21] Eisai, Hatfield, Herts, England
[22] Merck, Kenilworth, NJ USA
[23] Eisai, Woodcliff Lake, NJ USA
来源
NEW ENGLAND JOURNAL OF MEDICINE | 2022年 / 386卷 / 05期
关键词
PHASE-II; OPEN-LABEL; COMBINATION; MULTICENTER; CARCINOMA; EFFICACY; SAFETY; TRIAL; WOMEN;
D O I
10.1056/NEJMoa2108330
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Standard therapy for advanced endometrial cancer after failure of platinum-based chemotherapy remains unclear. METHODS In this phase 3 trial, we randomly assigned, in a 1:1 ratio, patients with advanced endometrial cancer who had previously received at least one platinum-based chemotherapy regimen to receive either lenvatinib (20 mg, administered orally once daily) plus pembrolizumab (200 mg, administered intravenously every 3 weeks) or chemotherapy of the treating physician's choice (doxorubicin at 60 mg per square meter of body-surface area, administered intravenously every 3 weeks, or paclitaxel at 80 mg per square meter, administered intravenously weekly [with a cycle of 3 weeks on and 1 week off]). The two primary end points were progression-free survival as assessed on blinded independent central review according to the Response Evaluation Criteria in Solid Tumors, version 1.1, and overall survival. The end points were evaluated in patients with mismatch repair-proficient (pMMR) disease and in all patients. Safety was also assessed. RESULTS A total of 827 patients (697 with pMMR disease and 130 with mismatch repair-deficient disease) were randomly assigned to receive lenvatinib plus pembrolizumab (411 patients) or chemotherapy (416 patients). The median progression-free survival was longer with lenvatinib plus pembrolizumab than with chemotherapy (pMMR population: 6.6 vs. 3.8 months; hazard ratio for progression or death, 0.60; 95% confidence interval [CI], 0.50 to 0.72; P<0.001; overall: 7.2 vs. 3.8 months; hazard ratio, 0.56; 95% CI, 0.47 to 0.66; P<0.001). The median overall survival was longer with lenvatinib plus pembrolizumab than with chemotherapy (pMMR population: 17.4 vs. 12.0 months; hazard ratio for death, 0.68; 95% CI, 0.56 to 0.84; P<0.001; overall: 18.3 vs. 11.4 months; hazard ratio, 0.62; 95% CI, 0.51 to 0.75; P<0.001). Adverse events of grade 3 or higher occurred in 88.9% of the patients who received lenvatinib plus pembrolizumab and in 72.7% of those who received chemotherapy. CONCLUSIONS Lenvatinib plus pembrolizumab led to significantly longer progression-free survival and overall survival than chemotherapy among patients with advanced endometrial cancer.
引用
收藏
页码:437 / 448
页数:12
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