Durvalumab plus Gemcitabine and Cisplatin in Advanced Biliary Tract Cancer

杜瓦卢马布 吉西他滨 安慰剂 危险系数 医学 肿瘤科 胃肠病学 内科学 外科 癌症 置信区间 化疗 病理 替代医学 免疫疗法 无容量
作者
Do‐Youn Oh,Aiwu Ruth He,Shukui Qin,Li‐Tzong Chen,Takuji Okusaka,Arndt Vogel,Jin Won Kim,Salomon M. Stemmer,Myung Ah Lee,Masayuki Kitano,Howard A. Burris,Mohamed Bouattour,Suebpong Tanasanvimon,Mairéad G. McNamara,Renata Zaucha,Antonio Avallone,Benjamin Tan,Juan Cundom,Choong‐kun Lee,Hidenori Takahashi,Masafumi Ikeda,Jen‐Shi Chen,Julie Wang,Mallory Makowsky,Nana Rokutanda,Philip He,John F. Kurland,Gordon Cohen,Juan W. Valle
出处
期刊:NEJM evidence [New England Journal of Medicine]
卷期号:1 (8) 被引量:443
标识
DOI:10.1056/evidoa2200015
摘要

BackgroundPatients with advanced biliary tract cancer have a poor prognosis, and first-line standard of care (gemcitabine plus cisplatin) has remained unchanged for more than 10 years. The TOPAZ-1 trial evaluated durvalumab plus chemotherapy for patients with advanced biliary tract cancer.MethodsIn this double-blind, placebo-controlled, phase 3 study, we randomly assigned patients with previously untreated unresectable or metastatic biliary tract cancer or with recurrent disease 1:1 to receive durvalumab or placebo in combination with gemcitabine plus cisplatin for up to eight cycles, followed by durvalumab or placebo monotherapy until disease progression or unacceptable toxicity. The primary objective was to assess overall survival. Secondary end points included progression-free survival, objective response rate, and safety.ResultsOverall, 685 patients were randomly assigned to durvalumab (n=341) or placebo (n=344) with chemotherapy. As of data cutoff, 198 patients (58.1%) in the durvalumab group and 226 patients (65.7%) in the placebo group had died. The hazard ratio for overall survival was 0.80 (95% confidence interval [CI], 0.66 to 0.97; P=0.021). The estimated 24-month overall survival rate was 24.9% (95% CI, 17.9 to 32.5) for durvalumab and 10.4% (95% CI, 4.7 to 18.8) for placebo. The hazard ratio for progression-free survival was 0.75 (95% CI, 0.63 to 0.89; P=0.001). Objective response rates were 26.7% with durvalumab and 18.7% with placebo. The incidences of grade 3 or 4 adverse events were 75.7% and 77.8% with durvalumab and placebo, respectively.ConclusionsDurvalumab plus chemotherapy significantly improved overall survival versus placebo plus chemotherapy and showed improvements versus placebo plus chemotherapy in prespecified secondary end points including progression-free survival and objective response rate. The safety profiles of the two treatment groups were similar. (Funded by AstraZeneca; ClinicalTrials.gov number, NCT03875235.)
最长约 10秒,即可获得该文献文件

科研通智能强力驱动
Strongly Powered by AbleSci AI
更新
大幅提高文件上传限制,最高150M (2024-4-1)

科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
1秒前
刘66完成签到,获得积分10
1秒前
烂漫的凡桃完成签到,获得积分10
1秒前
2秒前
自信如冰关注了科研通微信公众号
4秒前
空行发布了新的文献求助10
5秒前
5秒前
Cc完成签到 ,获得积分20
6秒前
柯氏气团不是气团完成签到,获得积分10
8秒前
沐雨发布了新的文献求助10
9秒前
小初发布了新的文献求助10
10秒前
李健应助windmill采纳,获得10
11秒前
训练有素的D完成签到 ,获得积分20
11秒前
12秒前
12秒前
keyan完成签到 ,获得积分10
12秒前
byq完成签到,获得积分20
12秒前
nanonamo完成签到,获得积分10
13秒前
14秒前
yuan完成签到,获得积分10
16秒前
依旧完成签到 ,获得积分10
17秒前
俗签发布了新的文献求助10
17秒前
郝宝真发布了新的文献求助10
19秒前
rorolinlin完成签到,获得积分10
20秒前
认真乐双完成签到,获得积分10
21秒前
秋枫忆完成签到,获得积分10
22秒前
Allen完成签到,获得积分10
23秒前
如愿完成签到 ,获得积分0
24秒前
Vin完成签到 ,获得积分10
24秒前
漂亮的尔烟完成签到,获得积分10
24秒前
俗签完成签到,获得积分10
25秒前
安屿发布了新的文献求助10
25秒前
25秒前
27秒前
27秒前
自信如冰发布了新的文献求助10
28秒前
29秒前
落瑾玘发布了新的文献求助10
30秒前
32秒前
娜娜发布了新的文献求助10
32秒前
高分求助中
Evolution 10000
ISSN 2159-8274 EISSN 2159-8290 1000
Becoming: An Introduction to Jung's Concept of Individuation 600
Ore genesis in the Zambian Copperbelt with particular reference to the northern sector of the Chambishi basin 500
A new species of Coccus (Homoptera: Coccoidea) from Malawi 500
A new species of Velataspis (Hemiptera Coccoidea Diaspididae) from tea in Assam 500
PraxisRatgeber: Mantiden: Faszinierende Lauerjäger 500
热门求助领域 (近24小时)
化学 医学 生物 材料科学 工程类 有机化学 生物化学 物理 内科学 纳米技术 计算机科学 化学工程 复合材料 基因 遗传学 催化作用 物理化学 免疫学 量子力学 细胞生物学
热门帖子
关注 科研通微信公众号,转发送积分 3162790
求助须知:如何正确求助?哪些是违规求助? 2813724
关于积分的说明 7901861
捐赠科研通 2473365
什么是DOI,文献DOI怎么找? 1316788
科研通“疑难数据库(出版商)”最低求助积分说明 631520
版权声明 602175