Camrelizumab plus apatinib as second-line treatment for advanced oesophageal squamous cell carcinoma (CAP 02): a single-arm, open-label, phase 2 trial.

阿帕蒂尼 医学 内科学 不利影响 临床终点 临床研究阶段 肿瘤科 索拉非尼 化疗 胃肠病学 外科
作者
Xiangrui Meng,Tao Wu,Yonggui Hong,Qingxia Fan,Zhonghai Ren,Yanzhen Guo,Xiuli Yang,Pei Shi,Jiamei Yang,Xianzhe Yin,Zhiquan Luo,Jin Xia,Yue Zhou,Mengli Xu,Enjie Liu,Guozhong Jiang,Shenglei Li,Feng Zhao,Chi Ma,Chuanxiang Ma,Zhiguo Hou,Jing Li,Junsheng Wang,Feng Wang
出处
期刊:The Lancet Gastroenterology & Hepatology [Elsevier BV]
卷期号:7 (3): 245-253
标识
DOI:10.1016/s2468-1253(21)00378-2
摘要

Camrelizumab, an anti-PD-1 antibody, has shown moderate efficacy in oesophageal squamous cell carcinoma. Apatinib, a selective inhibitor of VEGFR2, has a synergistic effect with immunotherapy. We aimed to assess the combination of camrelizumab and apatinib as second-line treatment for advanced oesophageal squamous cell carcinoma.This single-arm, open-label, phase 2 study was conducted at eight centres in China. Eligible patients were aged 18-75 years, with an Eastern Cooperative Oncology Group performance status of 0 or 1, who had unresectable locally advanced, locally recurrent, or metastatic oesophageal squamous cell carcinoma, and had progressed after or were intolerant to first-line chemotherapy. Patients received intravenous camrelizumab 200 mg once every 2 weeks plus oral apatinib 250 mg once daily for a 28-day cycle until disease progression, unacceptable adverse events, or withdrawal of consent. The primary endpoint was investigator-assessed confirmed objective response rate. Efficacy was analysed in patients who had received at least one dose of study drug, and safety was analysed in patients who received the study drug and had at least one post-baseline safety assessment. The study of this cohort is complete and this trial is registered with ClinicalTrials.gov, number NCT03736863.Between Dec 5, 2019, and Feb 10, 2021, 52 patients were enrolled and included in analyses. At data cutoff (June 20, 2021), median follow-up was 7·5 months (IQR 4·0-11·2). 18 (34·6%, [95% CI 22·0-49·1]) of 52 patients had a confirmed objective response. 23 (44%) of 52 patients had grade 3 or worse treatment-related adverse events. The most common grade 3 or worse treatment-related adverse events were increased aspartate aminotransferase (10 [19%]), increased gamma-glutamyltransferase (10 [19%]), and increased alanine aminotransferase (five [10%]). No treatment-related deaths occurred.Camrelizumab combined with apatinib showed promising activity and manageable toxicity, and might be a potential second-line treatment option for patients with advanced oesophageal squamous cell carcinoma. Another cohort of this study, enrolling patients previously treated with first-line immunotherapy, is ongoing.Jiangsu Hengrui Pharmaceuticals.
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
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
铁臂阿童木完成签到,获得积分10
刚刚
星辰大海应助厉凯文采纳,获得10
1秒前
2秒前
2秒前
Y1ST完成签到 ,获得积分10
3秒前
白桃完成签到 ,获得积分10
4秒前
5秒前
风趣的孤丝完成签到,获得积分10
5秒前
星辰大海应助kin采纳,获得10
5秒前
6秒前
媛媛完成签到,获得积分10
6秒前
秋风应助freya采纳,获得10
6秒前
丘比特应助KBRS采纳,获得10
7秒前
qzy发布了新的文献求助10
8秒前
ANNN发布了新的文献求助10
8秒前
可爱的函函应助Phoebe采纳,获得30
8秒前
8秒前
无奇完成签到,获得积分10
8秒前
英姑应助Boyu_Li采纳,获得10
8秒前
9秒前
小Q发布了新的文献求助10
9秒前
Aha发布了新的文献求助10
9秒前
10秒前
zyy完成签到,获得积分10
10秒前
11秒前
11秒前
11秒前
12秒前
健忘雁梅完成签到,获得积分10
13秒前
cidin完成签到,获得积分10
13秒前
13秒前
Leyoutong发布了新的文献求助10
13秒前
无奇发布了新的文献求助10
13秒前
邱邱应助liubr_kyt采纳,获得20
14秒前
14秒前
14秒前
陈小鱼完成签到 ,获得积分10
15秒前
义气MI猴桃完成签到,获得积分10
15秒前
Limbo发布了新的文献求助10
16秒前
16秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
Organizational Behavior 510
Management and the Arts 510
Matrix Methods in Data Mining and Pattern Recognition Second Edition 510
Rosenblum, Global Change Biology 500
CLSI VET01S-2024 Performance Standards for Antimicrobial Disk and Dilution Susceptibility Tests for Bacteria Isolated From Animals (7th Ed) 500
DIPPR Project 801 - Full Version 380
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 计算机科学 化学工程 工程类 有机化学 物理 复合材料 生物化学 内科学 细胞生物学 基因 遗传学 免疫学 冶金 光电子学 癌症研究
热门帖子
关注 科研通微信公众号,转发送积分 7767913
求助须知:如何正确求助?哪些是违规求助? 9311361
关于积分的说明 20323200
捐赠科研通 7352826
什么是DOI,文献DOI怎么找? 3315483
关于科研通互助平台的介绍 2464770
邀请新用户注册赠送积分活动 2330183