Neoadjuvant PD-1 Inhibitor Plus Apatinib and Chemotherapy Versus Apatinib Plus Chemotherapy in Treating Patients With Locally Advanced Gastric Cancer: A Prospective, Cohort Study

阿帕蒂尼 医学 内科学 危险系数 化疗 肿瘤科 胃肠病学 癌症 不利影响 比例危险模型 白细胞减少症 外科 置信区间
作者
Chunjing Wang,Zhen Wang,Yue Zhao,Fujing Wang
出处
期刊:Journal of Gastric Cancer [The Korean Gastric Cancer Association]
卷期号:23 (2): 328-328 被引量:6
标识
DOI:10.5230/jgc.2023.23.e17
摘要

This study aimed to evaluate the efficacy and safety of neoadjuvant programmed cell death-1 (PD-1) inhibitors plus apatinib and chemotherapy (PAC) in patients with locally advanced gastric cancer (LAGC).Seventy-three patients with resectable LAGC were enrolled and named the PAC group (n=39) or apatinib plus chemotherapy (AC) group (n=34) based on the treatment they chose. Neoadjuvant therapy was administered in a 21-day cycle for 3 consecutive cycles, after which surgery was performed.The PAC group exhibited a higher objective response rate than the AC group (74.4% vs. 58.8%, P=0.159). Moreover, the PAC group showed a numerically better response profile than the AC group (P=0.081). Strikingly, progression-free survival (PFS) (P=0.019) and overall survival (OS) (P=0.049) were prolonged, whereas disease-free survival (DFS) tended to be longer in the PAC group than in the AC group (P=0.056). Briefly, the 3-year PFS, DFS, and OS rates were 76.1%, 76.1%, and 86.7% in the PAC group and 46.9%, 49.9%, and 70.3% in the AC group, respectively. Furthermore, PAC (vs. AC) treatment (hazard ratio=0.286, P=0.034) was independently associated with prolonged PFS in multivariate Cox regression analyses. The incidence of adverse events did not differ between the two groups (all P>0.05), where leukopenia, anemia, hypertension, and other adverse events were commonly observed in the PAC group.Neoadjuvant PAC therapy may achieve a preferable pathological response, delayed progression, and prolonged survival compared to AC therapy with a similar safety profile in patients with LAGC; however, further validation is warranted.
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
务实天空完成签到,获得积分10
刚刚
wp4455777完成签到,获得积分10
刚刚
Xu_W卜完成签到,获得积分10
刚刚
ChatGPT发布了新的文献求助10
1秒前
小河流水完成签到 ,获得积分10
1秒前
pellaeon完成签到,获得积分10
2秒前
鱼鱼和石头完成签到 ,获得积分10
6秒前
wei998完成签到,获得积分20
8秒前
SciGPT应助Kelly采纳,获得10
8秒前
YXHTCM完成签到,获得积分10
9秒前
carly完成签到 ,获得积分10
10秒前
英勇的半兰完成签到,获得积分10
12秒前
玉玉完成签到,获得积分10
12秒前
居然是我完成签到,获得积分10
13秒前
慕青应助郭宏鹏采纳,获得10
13秒前
平淡的思真完成签到 ,获得积分10
13秒前
13秒前
天青色等烟雨完成签到,获得积分10
14秒前
安详靖柏完成签到,获得积分10
14秒前
zero完成签到 ,获得积分10
14秒前
悦耳的保温杯完成签到 ,获得积分10
15秒前
JXDYYZK完成签到,获得积分10
16秒前
张璟博发布了新的文献求助10
16秒前
做的出来完成签到,获得积分10
16秒前
李嘿嘿完成签到 ,获得积分10
18秒前
氢离子完成签到,获得积分10
18秒前
18秒前
墨影完成签到,获得积分10
19秒前
苏槑特完成签到,获得积分10
21秒前
Kelly发布了新的文献求助10
21秒前
陈粒完成签到 ,获得积分10
22秒前
xdedd完成签到,获得积分10
23秒前
小巧世倌完成签到,获得积分10
23秒前
水知寒完成签到,获得积分0
24秒前
风景的谷建芬完成签到,获得积分10
24秒前
宁赴湘完成签到 ,获得积分10
24秒前
Monkey_Z完成签到,获得积分10
25秒前
春山可望完成签到,获得积分10
25秒前
迷人的小土豆完成签到,获得积分10
25秒前
C胖胖完成签到,获得积分10
25秒前
高分求助中
Principles of Economics, 11th Edition 10000
University Physics with Modern Physics, 16th edition 10000
(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
Arthritis and Related Conditions, An Issue of Orthopedic Clinics 1000
Development of a Bridge Weigh-In-Motion System: A technology to convert the bridge response to the passage of traffic into data on vehicle configurations, speeds, times of travel and weights 1000
ズームレンズの光学設計に関する研究 800
Fundamentals of Pharmaceutical and Biologics Regulations: A Global Perspective, Second Edition 700
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 内科学 物理 复合材料 催化作用 细胞生物学 无机化学 光电子学 物理化学 电极 基因
热门帖子
关注 科研通微信公众号,转发送积分 7290862
求助须知:如何正确求助?哪些是违规求助? 8909923
关于积分的说明 18857666
捐赠科研通 6958043
什么是DOI,文献DOI怎么找? 3209179
关于科研通互助平台的介绍 2378976
邀请新用户注册赠送积分活动 2184921