Efficacy and safety of anlotinib combined with PD‐1/PD‐L1 inhibitors as second‐line and subsequent therapy in advanced small‐cell lung cancer

联合疗法 医学 紫杉醇 内科学 肿瘤科 不利影响 靶向治疗 肺癌 化疗 癌症
作者
Lian Yu,Jianlin Xu,Rong Qiao,Baohui Han,Hua Zhong,Runbo Zhong
出处
期刊:Cancer Medicine [Wiley]
卷期号:12 (5): 5372-5383 被引量:14
标识
DOI:10.1002/cam4.5360
摘要

Treatments for advanced small-cell lung cancer (SCLC) patients who are resistant to first-line chemotherapy are limited. Given that antiangiogenic agents and immune-checkpoint inhibitors (ICIs) can confer synergistic therapeutic benefits, combination therapy should be considered. We explored the efficacy and safety of combination therapy with anlotinib and programmed cell death protein 1 (PD-1)/programmed cell death-ligand 1 (PD-L1) inhibitors as second-line and subsequent therapy for advanced SCLC.We reviewed advanced SCLC patients at Shanghai Chest Hospital who had received anlotinib in combination with ICIs from November 2016 to November 2020 as second- and subsequent-line treatment. Patients with advanced SCLC who had received paclitaxel monotherapy as second-line treatment were included as the control group.A total of 141 patients were included in the final analysis (40 in the combination therapy group and 101 in the paclitaxel monotherapy group). The median progression-free survival (PFS) times for the combination therapy and paclitaxel monotherapy groups were 3.40 and 2.83 months (p = 0.022), respectively, while the median overall survival (OS) times for the combination therapy and paclitaxel monotherapy groups were 8.20 and 5.87 months (p = 0.048), respectively. Hypertension and hepatic dysfunction were the most pronounced adverse events of combination therapy and two patients changed regimens due to severe fatigue and anorexia.The combination of anlotinib and PD-1/PD-L1 blockade has promising efficacy and safety as a second-line or subsequent therapy for SCLC.
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
daisy发布了新的文献求助10
1秒前
泥過完成签到 ,获得积分10
3秒前
颠颠完成签到,获得积分10
3秒前
4秒前
共享精神应助素和姣姣采纳,获得10
4秒前
大个应助robi采纳,获得10
7秒前
脑洞疼应助每天都想下班采纳,获得10
7秒前
严剑封完成签到,获得积分10
8秒前
风起完成签到 ,获得积分10
8秒前
daisy完成签到,获得积分10
9秒前
allia完成签到 ,获得积分10
10秒前
11秒前
英姑应助YI点半的飞机场采纳,获得10
11秒前
11秒前
momo完成签到,获得积分20
12秒前
13秒前
共享精神应助风趣小小采纳,获得10
13秒前
bobo发布了新的文献求助10
15秒前
16秒前
zuhangzhao完成签到 ,获得积分10
17秒前
robi发布了新的文献求助10
17秒前
高挑的不凡完成签到,获得积分10
17秒前
末末完成签到,获得积分10
20秒前
Hello应助科研通管家采纳,获得10
21秒前
21秒前
华仔应助科研通管家采纳,获得30
21秒前
科研通AI2S应助科研通管家采纳,获得10
21秒前
zho应助科研通管家采纳,获得10
22秒前
可乐应助科研通管家采纳,获得10
22秒前
大模型应助科研通管家采纳,获得10
22秒前
wanci应助科研通管家采纳,获得10
22秒前
英姑应助科研通管家采纳,获得10
22秒前
22秒前
22秒前
22秒前
不配.应助LL采纳,获得10
22秒前
上官若男应助3kou采纳,获得10
23秒前
不配.应助yao chen采纳,获得10
25秒前
28秒前
小梦完成签到,获得积分10
28秒前
高分求助中
Sustainability in Tides Chemistry 2800
The Young builders of New china : the visit of the delegation of the WFDY to the Chinese People's Republic 1000
Rechtsphilosophie 1000
Bayesian Models of Cognition:Reverse Engineering the Mind 888
Le dégorgement réflexe des Acridiens 800
Defense against predation 800
Very-high-order BVD Schemes Using β-variable THINC Method 568
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 3134935
求助须知:如何正确求助?哪些是违规求助? 2785802
关于积分的说明 7774295
捐赠科研通 2441699
什么是DOI,文献DOI怎么找? 1298093
科研通“疑难数据库(出版商)”最低求助积分说明 625075
版权声明 600825