Sintilimab Plus Chemotherapy for Unresectable Gastric or Gastroesophageal Junction Cancer: The ORIENT-16 Randomized Clinical Trial

Gastric and gastroesophageal junction cancers are diagnosed in more than 1 million people worldwide annually, and few effective treatments are available. Sintilimab, a recombinant human IgG4 monoclonal antibody that binds to programmed cell death 1 (PD-1), in combination with chemotherapy, has demon...

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Veröffentlicht in:JAMA : the journal of the American Medical Association 2023-12, Vol.330 (21), p.2064-2074
Hauptverfasser: Xu, Jianming, Jiang, Haiping, Pan, Yueyin, Gu, Kangsheng, Cang, Shundong, Han, Lei, Shu, Yongqian, Li, Jiayi, Zhao, Junhui, Pan, Hongming, Luo, Suxia, Qin, Yanru, Guo, Qunyi, Bai, Yuxian, Ling, Yang, Yang, Jianwei, Yan, Zhilong, Yang, Lei, Tang, Yong, He, Yifu, Zhang, Liangming, Liang, Xinjun, Niu, Zuoxing, Zhang, Jingdong, Mao, Yong, Guo, Yingmei, Peng, Bo, Li, Ziran, Liu, Ying, Wang, Yan, Zhou, Hui
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Sprache:eng
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Zusammenfassung:Gastric and gastroesophageal junction cancers are diagnosed in more than 1 million people worldwide annually, and few effective treatments are available. Sintilimab, a recombinant human IgG4 monoclonal antibody that binds to programmed cell death 1 (PD-1), in combination with chemotherapy, has demonstrated promising efficacy. To compare overall survival of patients with unresectable locally advanced or metastatic gastric or gastroesophageal junction cancers who were treated with sintilimab with chemotherapy vs placebo with chemotherapy. Also compared were a subset of patients with a PD ligand 1 (PD-L1) combined positive score (CPS) of 5 or more (range, 1-100). Randomized, double-blind, placebo-controlled, phase 3 clinical trial conducted at 62 hospitals in China that enrolled 650 patients with unresectable locally advanced or metastatic gastric or gastroesophageal junction adenocarcinoma between January 3, 2019, and August 5, 2020. Final follow-up occurred on June 20, 2021. Patients were randomized 1:1 to either sintilimab (n = 327) or placebo (n = 323) combined with capecitabine and oxaliplatin (the XELOX regimen) every 3 weeks for a maximum of 6 cycles. Maintenance therapy with sintilimab or placebo plus capecitabine continued for up to 2 years. The primary end point was overall survival time from randomization. Of the 650 patients (mean age, 59 years; 483 [74.3%] men), 327 were randomized to sintilimab plus chemotherapy and 323 to placebo plus chemotherapy. Among the randomized patients, 397 (61.1%) had tumors with a PD-L1 CPS of 5 or more; 563 (86.6%) discontinued study treatment and 388 (59.7%) died; 1 patient (
ISSN:0098-7484
1538-3598
DOI:10.1001/jama.2023.19918