https://scholars.lib.ntu.edu.tw/handle/123456789/543454
標題: | Nivolumab in patients with advanced gastric or gastro-oesophageal junction cancer refractory to, or intolerant of, at least two previous chemotherapy regimens (ONO-4538-12, ATTRACTION-2): a randomised, double-blind, placebo-controlled, phase 3 trial | 作者: | Kang Y.-K. Boku N. Satoh T. Ryu M.-H. Chao Y. Kato K. Chung H.C. Chen J.-S. Muro K. Kang W.K. KUN-HUEI YEH Yoshikawa T. Oh S.C. Bai L.-Y. Tamura T. Lee K.-W. Hamamoto Y. Kim J.G. Chin K. Oh D.-Y. Minashi K. Cho J.Y. Tsuda M. Chen L.-T. |
公開日期: | 2017 | 出版社: | Lancet Publishing Group | 卷: | 390 | 期: | 10111 | 起(迄)頁: | 2461-2471 | 來源出版物: | The Lancet | 摘要: | Background Patients with advanced gastric or gastro-oesophageal junction cancer refractory to, or intolerant of, two or more previous regimens of chemotherapy have a poor prognosis, and current guidelines do not recommend any specific treatments for these patients. We assessed the efficacy and safety of nivolumab, a fully human IgG4 monoclonal antibody inhibitor of programmed death-1 (PD-1), in patients with advanced gastric or gastro-oesophageal junction cancer who had been previously been treated with two or more chemotherapy regimens. Methods In this randomised, double-blind, placebo-controlled, phase 3 trial done at 49 clinical sites in Japan, South Korea, and Taiwan, eligible patients (aged ?20 years with unresectable advanced or recurrent gastric or gastro-oesophageal junction cancer refractory to, or intolerant of, standard therapy [including two or more previous chemotherapy regimens], with an Eastern Cooperative Oncology Group [ECOG] performance status of 0–1, and naive to anti-PD-1 therapy or other therapeutic antibodies and pharmacotherapies for the regulation of T cells) were recruited. Patients were randomly assigned (2:1) using an interactive web response system to receive 3 mg/kg nivolumab or placebo intravenously every 2 weeks, stratified by country, ECOG performance status, and number of organs with metastases. Study treatment was continued until progressive disease per investigator assessment or onset of toxicities requiring permanent discontinuation. Patients and investigators were masked to group assignment. The primary endpoint was overall survival in the intention-to-treat population. Safety was analysed in all patients who received at least one dose of study treatment. This study is ongoing but not recruiting new patients, and is registered with ClinicalTrials.gov, number NCT02267343. Findings Between Nov 4, 2014, and Feb 26, 2016, we randomly assigned 493 patients to receive nivolumab (n=330) or placebo (n=163). At the data cutoff (Aug 13, 2016), median follow-up in surviving patients was 8·87 months (IQR 6·57–12·37) in the nivolumab group and 8·59 months (5·65–11·37) in the placebo group. Median overall survival was 5·26 months (95% CI 4·60–6·37) in the nivolumab group and 4·14 months (3·42–4·86) in the placebo group (hazard ratio 0·63, 95% CI 0·51–0·78; p<0·0001). 12-month overall survival rates were 26·2% (95% CI 20·7–32·0) with nivolumab and 10·9% (6·2–17·0) with placebo. Grade 3 or 4 treatment-related adverse events occurred in 34 (10%) of 330 patients who received nivolumab and seven (4%) of 161 patients who received placebo; treatment-related adverse events led to death in five (2%) of 330 patients in the nivolumab group and two (1%) of 161 patients in the placebo group. No new safety signals were observed. Interpretation In this phase 3 study, the survival benefits indicate that nivolumab might be a new treatment option for heavily pretreated patients with advanced gastric or gastro-oesophageal junction cancer. Ongoing trials that include non-Asian patients are investigating nivolumab for advanced gastric or gastro-oesophageal junction cancer in various settings and earlier treatment lines. Funding Ono Pharmaceutical and Bristol-Myers Squibb. ? 2017 Elsevier Ltd |
URI: | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85030626436&doi=10.1016%2fS0140-6736%2817%2931827-5&partnerID=40&md5=3afb220cb54fa95bf08471358b6c7d0a https://scholars.lib.ntu.edu.tw/handle/123456789/543454 |
ISSN: | 0140-6736 | DOI: | 10.1016/S0140-6736(17)31827-5 | SDG/關鍵字: | alanine aminotransferase; aspartate aminotransferase; immunoglobulin G4; irinotecan; nivolumab; placebo; programmed death 1 ligand 1; pyrimidine; ramucirumab; antineoplastic agent; monoclonal antibody; nivolumab; acute hepatitis; adult; advanced cancer; aged; Article; autoimmune thyroiditis; cancer chemotherapy; cancer fatigue; cancer grading; cancer surgery; cancer survival; colitis; controlled study; decreased appetite; diarrhea; digestive system perforation; double blind procedure; drug efficacy; drug safety; dyspnea; electrocorticography; female; fever; gastrectomy; gastroesophageal junction; gastroesophageal junction cancer; heart arrest; human; hyperthyroidism; hypopituitarism; intention to treat analysis; interstitial lung disease; maculopapular rash; major clinical study; male; muscle weakness; nausea; overall survival; patient history of chemotherapy; phase 3 clinical trial; pneumonia; priority journal; pruritus; randomized controlled trial; side effect; South Korea; stomach cancer; Taiwan; urinary tract infection; adenocarcinoma; clinical trial; middle aged; mortality; stomach tumor; treatment failure; Adenocarcinoma; Aged; Antibodies, Monoclonal; Antineoplastic Agents; Double-Blind Method; Esophagogastric Junction; Female; Humans; Male; Middle Aged; Stomach Neoplasms; Treatment Failure |
顯示於: | 腫瘤醫學研究所 |
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