{"title":"Correction to Lancet Gastroenterol Hepatol 2024; 9: 705–17","authors":"","doi":"10.1016/s2468-1253(25)00047-0","DOIUrl":null,"url":null,"abstract":"<em>Kang Y-K, Terashima M, Kim Y-W, et al. Adjuvant nivolumab plus chemotherapy versus placebo plus chemotherapy for stage III gastric or gastro-oesophageal junction cancer after gastrectomy with D2 or more extensive lymph-node dissection (ATTRACTION-5): a randomised, multicentre, double-blind, placebo-controlled, phase 3 trial.</em> Lancet Gastroenterol Hepatol <em>2024; <strong>9:</strong> 705–17</em>—In this Article, the penultimate sentence of the Findings section of the Summary should read: “Discontinuation due to treatment-related adverse events was more frequent in the nivolumab plus chemotherapy group (34 [9%] of 371 patients) than the placebo plus chemotherapy group (13 [4%] of 374 patients).” Reasons for treatment discontinuation have been clarified in figure 1 and some rounding errors have been corrected in tables 1 and 2. In figure 2B, the CI for the hazard ratio has been corrected to read “95% CI”. The third sentence of the second paragraph of the Results section should read: “339 (90%) of 377 patients in the nivolumab group and 338 (89%) of 378 patients in the placebo group resided in Japan or South Korea.” The third paragraph of the Results section has been updated to read “Overall, 495 (66%) of 755 patients (228 [60%] of 377 in the nivolumab plus chemotherapy group; 267 [71%] of 378 in the placebo plus chemotherapy group) completed the prespecified adjuvant therapy and 128 (17%) of 755 patients (75 [20%] of those in the nivolumab plus chemotherapy group; 53 [14%] of those in the placebo plus chemotherapy group) discontinued both nivolumab and chemotherapy or placebo and chemotherapy (figure 1). 18 (24%) of 75 patients discontinued both components of therapy in the nivolumab plus chemotherapy group solely due to unacceptable toxicity, as did five (9%) of 53 in the placebo plus chemotherapy group.” The start of the fifth line of the ninth paragraph of the Results section has been revised to state “Similarly, discontinuation due to treatment-related adverse events was…”. In table 3, the number of patients in the placebo plus chemotherapy group who had grade 3 diarrhoea has been corrected to read “13 (3%)”. Details of deaths in the trial have been updated; the final two sentences of the Results section has been replaced with: “There was one death (subarachnoid haemorrhage) in the placebo plus chemotherapy group and two (asphyxia; pneumonitis) in the nivolumab plus chemotherapy group. Only the death due to pneumonitis in the nivolumab plus chemotherapy group was considered to be related to treatment.” These corrections have been made as of March 12, 2025.","PeriodicalId":56028,"journal":{"name":"Lancet Gastroenterology & Hepatology","volume":"213 1","pages":""},"PeriodicalIF":38.6000,"publicationDate":"2025-03-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Lancet Gastroenterology & Hepatology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/s2468-1253(25)00047-0","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Kang Y-K, Terashima M, Kim Y-W, et al. Adjuvant nivolumab plus chemotherapy versus placebo plus chemotherapy for stage III gastric or gastro-oesophageal junction cancer after gastrectomy with D2 or more extensive lymph-node dissection (ATTRACTION-5): a randomised, multicentre, double-blind, placebo-controlled, phase 3 trial. Lancet Gastroenterol Hepatol 2024; 9: 705–17—In this Article, the penultimate sentence of the Findings section of the Summary should read: “Discontinuation due to treatment-related adverse events was more frequent in the nivolumab plus chemotherapy group (34 [9%] of 371 patients) than the placebo plus chemotherapy group (13 [4%] of 374 patients).” Reasons for treatment discontinuation have been clarified in figure 1 and some rounding errors have been corrected in tables 1 and 2. In figure 2B, the CI for the hazard ratio has been corrected to read “95% CI”. The third sentence of the second paragraph of the Results section should read: “339 (90%) of 377 patients in the nivolumab group and 338 (89%) of 378 patients in the placebo group resided in Japan or South Korea.” The third paragraph of the Results section has been updated to read “Overall, 495 (66%) of 755 patients (228 [60%] of 377 in the nivolumab plus chemotherapy group; 267 [71%] of 378 in the placebo plus chemotherapy group) completed the prespecified adjuvant therapy and 128 (17%) of 755 patients (75 [20%] of those in the nivolumab plus chemotherapy group; 53 [14%] of those in the placebo plus chemotherapy group) discontinued both nivolumab and chemotherapy or placebo and chemotherapy (figure 1). 18 (24%) of 75 patients discontinued both components of therapy in the nivolumab plus chemotherapy group solely due to unacceptable toxicity, as did five (9%) of 53 in the placebo plus chemotherapy group.” The start of the fifth line of the ninth paragraph of the Results section has been revised to state “Similarly, discontinuation due to treatment-related adverse events was…”. In table 3, the number of patients in the placebo plus chemotherapy group who had grade 3 diarrhoea has been corrected to read “13 (3%)”. Details of deaths in the trial have been updated; the final two sentences of the Results section has been replaced with: “There was one death (subarachnoid haemorrhage) in the placebo plus chemotherapy group and two (asphyxia; pneumonitis) in the nivolumab plus chemotherapy group. Only the death due to pneumonitis in the nivolumab plus chemotherapy group was considered to be related to treatment.” These corrections have been made as of March 12, 2025.
姜永康,Terashima M, Kim yw,等。辅助纳武单抗加化疗vs安慰剂加化疗治疗胃切除术后伴有D2或更广泛淋巴结清扫的III期胃癌或胃食管结癌(ATTRACTION-5):一项随机、多中心、双盲、安慰剂对照的3期试验。Lancet Gastroenterol Hepatol 2024;[9:705 - 17]在这篇文章中,摘要发现部分的倒数第二句应该是:“由于治疗相关不良事件而停药,在纳武单抗加化疗组(371例患者中34例[9%])比安慰剂加化疗组(374例患者中13例[4%])更频繁。”停止治疗的原因已在图1中澄清,一些舍入误差已在表1和表2中得到纠正。在图2B中,风险比的CI已被修正为“95% CI”。结果部分第二段的第三句应该是:“nivolumab组377例患者中有339例(90%)居住在日本或韩国,安慰剂组378例患者中有338例(89%)居住在日本或韩国。”结果部分的第三段已更新为“总体而言,755例患者中有495例(66%)(377例患者中有228例(60%)在纳武单抗加化疗组;安慰剂加化疗组378名患者中有267名(71%)完成了预先指定的辅助治疗,755名患者中有128名(17%)完成了辅助治疗(纳武单抗加化疗组中有75名(20%)完成了辅助治疗;在安慰剂加化疗组中,53人(14%)停止了纳武单抗加化疗或安慰剂加化疗(图1)。75名患者中,18人(24%)仅仅因为不可接受的毒性而停止了纳武单抗加化疗组的治疗,在安慰剂加化疗组中,53名患者中有5人(9%)停止了治疗。”结果部分第9段第5行开头修改为“同样,由于治疗相关不良事件而停止治疗是……”。在表3中,安慰剂加化疗组出现3级腹泻的患者数量被更正为“13(3%)”。试验中死亡的详细情况已得到更新;结果部分的最后两句被替换为:“安慰剂加化疗组有1例死亡(蛛网膜下腔出血),2例死亡(窒息;肺炎)在纳武单抗加化疗组。只有纳武单抗加化疗组的肺炎死亡被认为与治疗有关。”这些更正已于2025年3月12日作出。
期刊介绍:
The Lancet Gastroenterology & Hepatology is an authoritative forum for key opinion leaders across medicine, government, and health systems to influence clinical practice, explore global policy, and inform constructive, positive change worldwide.
The Lancet Gastroenterology & Hepatology publishes papers that reflect the rich variety of ongoing clinical research in these fields, especially in the areas of inflammatory bowel diseases, NAFLD and NASH, functional gastrointestinal disorders, digestive cancers, and viral hepatitis.