Perioperative Durvalumab in Gastric and Gastroesophageal Junction Cancer

被引:4
作者
Janjigian, Yelena Y. [1 ,2 ]
Al-Batran, Salah-Eddin [3 ,4 ]
Wainberg, Zev A. [5 ]
Muro, Kei [6 ]
Molena, Daniela [2 ,7 ]
Van Cutsem, Eric [8 ,9 ]
Hyung, Woo Jin [10 ]
Wyrwicz, Lucjan [11 ]
Oh, Do-Youn [12 ,13 ]
Omori, Takeshi [14 ]
Moehler, Markus
Garrido, Marcelo
Oliveira, Sulene C. S.
Liberman, Moishe [15 ]
Oliden, Victor Castro [16 ]
Smyth, Elizabeth C. [17 ]
Stein, Alexander [18 ]
Bilici, Mehmet [19 ]
Alvarenga, Maria Lorena [20 ]
Kozlov, Vadim [21 ]
Rivera, Fernando
Kawazoe, Akihito [22 ]
Serrano, Olivier [23 ]
Heilbron, Eric [24 ]
Negro, Alejandra [24 ]
Kurland, John F. [24 ]
Tabernero, Josep [25 ]
机构
[1] Mem Sloan Kettering Canc Ctr, Gastrointestinal Oncol Serv, BAIC Rm 1001,300 E 66th St, New York, NY 10065 USA
[2] Weill Cornell Med, New York, NY USA
[3] Univ Canc Ctr UCT Frankfurt, Krankenhaus Nordwest, Frankfurt, Germany
[4] Frankfurt Inst Clin Canc Res IKF, Frankfurt, Germany
[5] Univ Calif Los Angeles, Dept Gastrointestinal Med Oncol, David Geffen Sch Med, Los Angeles, CA USA
[6] Aichi Canc Ctr Hosp, Dept Clin Oncol, Nagoya, Japan
[7] Mem Sloan Kettering Canc Ctr, Div Thorac Surg, New York, NY USA
[8] Univ Hosp Leuven, Dept Gastroenterol Digest Oncol, Leuven, Belgium
[9] Katholieke Univ Leuven, Leuven, Belgium
[10] Yonsei Univ, Coll Med, Dept Surg, Seoul, South Korea
[11] Mar Sklodowska Curie Natl Res Inst Oncol, Dept Oncol & Radiotherapy, Warsaw, Poland
[12] Seoul Natl Univ, Seoul Natl Univ Hosp, Dept Internal Med, Div Med Oncol,Coll Med, Seoul, South Korea
[13] Seoul Natl Univ, Canc Res Inst, Coll Med, Seoul, South Korea
[14] Osaka Int Canc Inst, Dept Gastroenterol Surg, Osaka, Japan
[15] Ctr Hosp Univ Montreal, Ctr Rech CHUM, Dept Surg, Div Thorac Surg, Montreal, PQ, Canada
[16] Natl Inst Neoplast Dis INEN, Lima, Peru
[17] Churchill Hosp, Oxford NIHR Biomed Res Ctr, Oxford, England
[18] Univ Med Ctr Hamburg Eppendorf, Univ Canc Ctr Hamburg UCCH, Hematol Oncol Practice Eppendorf HOPE, Hamburg, Germany
[19] Ataturk Univ, Fac Med, Div Med Oncol, Dept Internal Med, Erzurum, Turkiye
[20] Favaloro Fdn Univ Hosp, Dept Clin Oncol, Buenos Aires, Argentina
[21] State Budgetary Hlth Care Inst, Novosibirsk Reg Clin Oncol Dispensary, Novosibirsk, Russia
[22] Natl Canc Ctr Hosp East, Dept Gastroenterol & Gastrointestinal Oncol, Kashiwa, Japan
[23] AstraZeneca, Cytel, Paris, France
[24] AstraZeneca, Oncol R&D, Late Stage Dev, Gaithersburg, MD USA
[25] UVic UCC, Inst Oncol VHIO, Med Oncol Dept, IOB Quiron,Vall dHebron Hosp Campus, Barcelona, Spain
基金
美国国家卫生研究院;
关键词
PREOPERATIVE CHEMORADIOTHERAPY; OPEN-LABEL; ADENOCARCINOMA; ESOPHAGEAL; CHEMOTHERAPY;
D O I
10.1056/NEJMoa2503701
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Perioperative FLOT (fluorouracil, leucovorin, oxaliplatin, and docetaxel) is a standard therapy for resectable gastric and gastroesophageal junction adenocarcinomas, but recurrence rates remain high. Immunotherapy plus chemotherapy may improve outcomes. Methods In a phase 3, multinational, double-blind, randomized trial, we assigned participants with resectable gastric or gastroesophageal junction adenocarcinoma, in a 1:1 ratio, to receive durvalumab at a dose of 1500 mg or placebo every 4 weeks plus FLOT for 4 cycles (2 cycles each of neoadjuvant and adjuvant therapy), followed by durvalumab or placebo every 4 weeks for 10 cycles. The primary end point was event-free survival; secondary end points included overall survival and pathological complete response. Results A total of 474 participants were randomly assigned to the durvalumab group, and 474 to the placebo group (median follow-up, 31.5 months; interquartile range, 26.7 to 36.6). Two-year event-free survival (Kaplan-Meier estimate) was 67.4% among the participants in the durvalumab group and 58.5% among those in the placebo group (hazard ratio for event or death, 0.71; 95% confidence interval [CI], 0.58 to 0.86; P<0.001). Two-year overall survival was 75.7% in the durvalumab group and 70.4% in the placebo group (piecewise hazard ratio for death during months 0 to 12, 0.99 [95% CI, 0.70 to 1.39], and during the period from month 12 onward, 0.67 [95% CI, 0.50 to 0.90]; P=0.03 by a stratified log-rank test [exceeding the significance threshold of P<0.0001]). The percentage of participants with a pathological complete response was 19.2% in the durvalumab group and 7.2% in the placebo group (relative risk, 2.69 [95% CI, 1.86 to 3.90]). Adverse events with a maximum grade of 3 or 4 were reported in 340 participants (71.6%) in the durvalumab group and in 334 (71.2%) in the placebo group. The percentage of participants with delayed surgery was 10.1% and 10.8%, respectively, and the percentage with delayed initiation of adjuvant treatment was 2.3% and 4.6%. Conclusions Perioperative durvalumab plus FLOT led to significantly better event-free survival outcomes than FLOT alone among participants with resectable gastric or gastroesophageal junction adenocarcinoma. (Funded by AstraZeneca; MATTERHORN ClinicalTrials.gov number, NCT04592913.)
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收藏
页码:217 / 230
页数:14
相关论文
共 33 条
[1]   Perioperative chemotherapy with fluorouracil plus leucovorin, oxaliplatin, and docetaxel versus fluorouracil or capecitabine plus cisplatin and epirubicin for locally advanced, resectable gastric or gastro-oesophageal junction adenocarcinoma (FLOT4): a randomised, phase 2/3 trial [J].
Al-Batran, Salah-Eddin ;
Homann, Nils ;
Pauligk, Claudia ;
Goetze, Thorsten O. ;
Meiler, Johannes ;
Kasper, Stefan ;
Kopp, Hans-Georg ;
Mayer, Frank ;
Haag, Georg Martin ;
Luley, Kim ;
Lindig, Udo ;
Schmiegel, Wolff ;
Pohl, Michael ;
Stoehlmacher, Jan ;
Folprecht, Gunnar ;
Probst, Stephan ;
Prasnikar, Nicole ;
Fischbach, Wolfgang ;
Mahlberg, Rolf ;
Trojan, Joerg ;
Koenigsmann, Michael ;
Martens, Uwe M. ;
Thuss-Patience, Peter ;
Egger, Matthias ;
Block, Andreas ;
Heinemann, Volker ;
Illerhaus, Gerald ;
Moehler, Markus ;
Schenk, Michael ;
Kullmann, Frank ;
Behringer, Dirk M. ;
Heike, Michael ;
Pink, Daniel ;
Teschendorf, Christian ;
Loehr, Carmen ;
Bernhard, Helga ;
Schuch, Gunter ;
Rethwisch, Volker ;
von Weikersthal, Ludwig Fischer ;
Hartmann, Joerg T. ;
Kneba, Michael ;
Daum, Severin ;
Schulmann, Karsten ;
Weniger, Joerg ;
Belle, Sebastian ;
Gaiser, Timo ;
Oduncu, Fuat S. ;
Guentner, Martina ;
Hozaeel, Wael ;
Reichart, Alexander .
LANCET, 2019, 393 (10184) :1948-1957
[2]  
Amin MB, 2017, AJCC Cancer Staging Manual
[3]   Safety and antitumour activity of durvalumab plus tremelimumab in non-small-cell lung cancer: a multicentre, phase 1b study [J].
Antonia, Scott ;
Goldberg, Sarah B. ;
Balmanoukian, Ani ;
Chaft, Jamie E. ;
Sanborn, Rachel E. ;
Gupta, Ashok ;
Narwal, Rajesh ;
Steele, Keith ;
Gu, Yu ;
Karakunnel, Joyson J. ;
Rizvi, Naiyer A. .
LANCET ONCOLOGY, 2016, 17 (03) :299-308
[4]   Global cancer statistics 2022: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries [J].
Bray, Freddie ;
Laversanne, Mathieu ;
Sung, Hyuna ;
Ferlay, Jacques ;
Siegel, Rebecca L. ;
Soerjomataram, Isabelle ;
Jemal, Ahmedin .
CA-A CANCER JOURNAL FOR CLINICIANS, 2024, 74 (03) :229-263
[5]  
College of American Pathologists (CAP), 2020, Protocol for the examination of specimens from patients with carcinoma of the stomach
[6]  
Food and Drug Administration, 2025, FDA approves durvalumab for muscle invasive bladder cancer
[7]  
Food and Drug Administration, 2020, FDA approves durvalumab for extensive-stage small cell lung cancer
[8]  
Food and Drug Administration, 2024, FDA approves durvalumab with chemotherapy for mismatch repair deficient primary advanced or recurrent endometrial cancer
[9]  
Food and Drug Administration, 2023, Opdivo (nivolumab): highlights of prescribing information
[10]  
Food and Drug Administration, 2024, Keytruda (pembrolizumab): highlights of prescribing information