Efficacy and biomarker exploration of camrelizumab combined with apatinib in the treatment of advanced primary liver cancer: a retrospective study

阿帕蒂尼 医学 内科学 回顾性队列研究 临床终点 置信区间 无进展生存期 外科 危险系数 胃肠病学 不利影响 癌症 化疗 随机对照试验
作者
Zhiming Zeng,Yanfeng Jiang,Cuizhen Liu,Guangzhi Zhu,Fu‐Chao Ma,Lihua Yang,Jinfeng Qiu,Jing Tang,Xinping Ye,Tao Peng,Jie Zeng,Jie Ma
出处
期刊:Anti-Cancer Drugs [Ovid Technologies (Wolters Kluwer)]
卷期号:32 (10): 1093-1098 被引量:5
标识
DOI:10.1097/cad.0000000000001127
摘要

This study was to explore the efficacy and safety of camrelizumab combined with apatinib in patients with advanced liver cancer. Moreover, the relationship between peripheral blood parameters and tumor response rate was also investigated. Patients with unresectable or recurrent primary liver cancer (PLC) who received treatment from July 2019 to July 2020 in the First Affiliated Hospital of Guangxi Medical University were included in this single-center retrospective study. The patients were treated with camrelizumab (200 mg, intravenous q2w) plus apatinib (250 mg, oral qd) until the occurrence of disease progression or unbearable toxicity. All the patients underwent blood routine test and detection of lactate dehydrogenase and serum albumin levels before treatment. The primary endpoints were objective response rate (ORR) and disease control rate (DCR). This study included a total of 45 patients. The overall ORR was 33.3% [95% confidence interval (CI),19.0-47.7] and the overall DCR was 57.8% (95% CI, 42.8-72.8). The ORR and DCR were higher in the first-line treatment than those in the second-line treatment (ORR: 45.5% vs. 21.7%, DCR: 63.6% vs. 52.3%). Median progression-free survival in the second-line treatment was 10.5 months (95% CI, 7.9-13.1, P = 0.022). Adverse events occurred in 39 (86.7%) patients. Grade 3/4 adverse reactions occurred in 7 (15.6%) patients. One patient (4.3%) was terminated from treatment due to adverse events. One patient (4.3%) died, which was potentially associated with adverse events. Subgroup analysis indicated that the remission rate in patients with high lymphocyte to monocyte ratio (H-LMR) was higher than that in patients with low lymphocyte to monocyte ratio (L-LMR) (56.25% vs. 25.93%, P = 0.047), and the remission rate in patients with high Prognostic Nutritional Index (H-PNI) was higher than that in patients with low Prognostic Nutritional Index (L-PNI) (66.7% vs. 26.5%, P = 0.046). Camrelizumab combined with apatinib in the treatment of PLC showed encouraging clinical efficacy, with tolerable toxicities. Levels of PNI and LMR may serve as predictors of the prognosis of advanced PLC patients who receive immunotherapy combined with targeted therapy.
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
兜兜完成签到,获得积分10
刚刚
dingdong发布了新的文献求助10
刚刚
刚刚
yuan发布了新的文献求助20
1秒前
HUAJIAO完成签到,获得积分10
1秒前
街舞腹肌修道帅哥完成签到,获得积分10
1秒前
zhangyulu完成签到 ,获得积分10
2秒前
2秒前
独特不斜完成签到,获得积分10
2秒前
海底落日发布了新的文献求助30
2秒前
共享精神应助紧张的妖妖采纳,获得10
2秒前
耶耶粘豆包完成签到 ,获得积分10
3秒前
dingdong发布了新的文献求助10
4秒前
xunxunmimi发布了新的文献求助50
4秒前
Z小姐发布了新的文献求助10
4秒前
幽壑之潜蛟应助123采纳,获得10
5秒前
是天使呢发布了新的文献求助10
5秒前
5秒前
研友_VZG7GZ应助坨坨西州采纳,获得10
6秒前
6秒前
华华完成签到,获得积分10
6秒前
刘明发布了新的文献求助10
6秒前
1604531786发布了新的文献求助10
8秒前
魁梧的小霸王完成签到,获得积分10
8秒前
星辰大海应助123采纳,获得10
8秒前
8秒前
是一只象完成签到,获得积分20
8秒前
科研通AI5应助海鸥海鸥采纳,获得10
9秒前
幸福遥完成签到,获得积分10
10秒前
10秒前
小王发布了新的文献求助10
10秒前
热心的代桃完成签到,获得积分10
10秒前
CodeCraft应助Olsters采纳,获得10
10秒前
11秒前
研友_IEEE快到碗里来完成签到,获得积分10
12秒前
哈哈大笑应助吴岳采纳,获得10
12秒前
12秒前
酷炫中蓝完成签到,获得积分10
12秒前
早川完成签到 ,获得积分10
13秒前
拼搏语薇完成签到,获得积分10
13秒前
高分求助中
Continuum Thermodynamics and Material Modelling 3000
Production Logging: Theoretical and Interpretive Elements 2700
Social media impact on athlete mental health: #RealityCheck 1020
Ensartinib (Ensacove) for Non-Small Cell Lung Cancer 1000
Unseen Mendieta: The Unpublished Works of Ana Mendieta 1000
Bacterial collagenases and their clinical applications 800
El viaje de una vida: Memorias de María Lecea 800
热门求助领域 (近24小时)
化学 材料科学 生物 医学 工程类 有机化学 生物化学 物理 纳米技术 计算机科学 内科学 化学工程 复合材料 基因 遗传学 物理化学 催化作用 量子力学 光电子学 冶金
热门帖子
关注 科研通微信公众号,转发送积分 3527849
求助须知:如何正确求助?哪些是违规求助? 3107938
关于积分的说明 9287239
捐赠科研通 2805706
什么是DOI,文献DOI怎么找? 1540033
邀请新用户注册赠送积分活动 716893
科研通“疑难数据库(出版商)”最低求助积分说明 709794