亲爱的研友该休息了!由于当前在线用户较少,发布求助请尽量完整的填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!身体可是革命的本钱,早点休息,好梦!

Local Ablative Therapy Combined With Pembrolizumab in Patients With Synchronous Oligometastatic Non-Small Cell Lung Cancer: A Recursive Partitioning Analysis

彭布罗利珠单抗 离格 医学 肺癌 肿瘤科 内科学 放射科 癌症 放射治疗 免疫疗法
作者
Hye In Lee,Eun Kyung Choi,Su Ssan Kim,Young Seob Shin,Jun‐Hee Park,Chang‐Min Choi,Shinkyo Yoon,Hyeong Ryul Kim,Young Hyun Cho,Si Yeol Song
出处
期刊:International Journal of Radiation Oncology Biology Physics [Elsevier BV]
卷期号:120 (3): 698-707
标识
DOI:10.1016/j.ijrobp.2024.05.015
摘要

Purpose: This study aimed to evaluate the efficacy of local ablative therapy (LAT) combined with pembrolizumab in patients with synchronous oligometastatic non-small cell lung cancer (NSCLC) and to identify patients who would most benefit from LAT. Methods and Materials: We retrospectively identified patients diagnosed with synchronous oligometastatic NSCLC (≤5 metastatic lesions and ≤3 organs involved) and treated with first-line pembrolizumab between January 2017 and December 2022. Patients who underwent LAT, including surgery or radiotherapy at all disease sites, were compared with those who did not undergo LAT. A recursive partitioning analysis (RPA) model was developed using prognostic factors for progression-free survival (PFS). Results: Among the 258 patients included, 78 received LAT with pembrolizumab and 180 received pembrolizumab alone. The median follow-up duration was 15.5 months (range, 3.0–71.2). In the entire cohort, LAT was independently associated with significantly improved PFS (hazard ratio [HR], 0.64; P = 0.015) and overall survival (OS) (HR, 0.61; P = 0.020). In the propensity score-matched cohort (N = 74 in each group), the median PFS was 19.9 months and 9.6 months, respectively (P = 0.003), and the median OS was 42.2 months and 20.5 months, respectively (P = 0.045), for the LAT and non-LAT groups. Based on the RPA model, incorporating the number of metastatic lesions, performance status, and PD-L1 expression level, patients were stratified into three risk groups with distinct PFS. LAT significantly improved PFS and OS in the low- and intermediate-risk groups; however, no difference was observed in the high-risk group. LAT was more effective as a consolidative treatment following pembrolizumab initiation than as an upfront therapy. Conclusion: LAT combined with pembrolizumab was associated with higher PFS and OS compared to pembrolizumab alone in selected patients with synchronous oligometastatic NSCLC. The RPA model could serve as a valuable clinical tool for identifying appropriate patients for LAT.
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
1461完成签到 ,获得积分10
41秒前
1分钟前
zhang发布了新的文献求助10
1分钟前
传奇3应助研友_Fan采纳,获得10
2分钟前
DYKNGIVDFY完成签到,获得积分10
3分钟前
山橘月发布了新的文献求助10
3分钟前
慕青应助科研通管家采纳,获得10
3分钟前
丘比特应助科研通管家采纳,获得30
3分钟前
hhh完成签到,获得积分10
3分钟前
3分钟前
Tiger完成签到,获得积分10
4分钟前
研友_Fan发布了新的文献求助10
4分钟前
DYKNGIVDFY发布了新的文献求助10
4分钟前
George发布了新的文献求助10
5分钟前
5分钟前
思源应助科研通管家采纳,获得10
5分钟前
5分钟前
xun完成签到,获得积分10
5分钟前
Linda发布了新的文献求助30
5分钟前
整齐的蜻蜓完成签到 ,获得积分10
5分钟前
6分钟前
Linda完成签到,获得积分10
6分钟前
科研通AI5应助菁菁采纳,获得30
6分钟前
科研通AI5应助科研通管家采纳,获得10
7分钟前
7分钟前
7分钟前
Owllight发布了新的文献求助10
7分钟前
7分钟前
研友_Fan完成签到,获得积分10
8分钟前
8分钟前
8分钟前
8分钟前
菁菁发布了新的文献求助30
9分钟前
9分钟前
jeff完成签到,获得积分20
9分钟前
无花果应助科研通管家采纳,获得10
9分钟前
打打应助科研通管家采纳,获得10
9分钟前
菁菁完成签到,获得积分10
9分钟前
John完成签到,获得积分10
9分钟前
thangxtz完成签到,获得积分10
10分钟前
高分求助中
Les Mantodea de Guyane Insecta, Polyneoptera 2500
Technologies supporting mass customization of apparel: A pilot project 450
A Field Guide to the Amphibians and Reptiles of Madagascar - Frank Glaw and Miguel Vences - 3rd Edition 400
A China diary: Peking 400
Brain and Heart The Triumphs and Struggles of a Pediatric Neurosurgeon 400
Cybersecurity Blueprint – Transitioning to Tech 400
Mixing the elements of mass customisation 400
热门求助领域 (近24小时)
化学 材料科学 医学 生物 工程类 有机化学 物理 生物化学 纳米技术 计算机科学 化学工程 内科学 复合材料 物理化学 电极 遗传学 量子力学 基因 冶金 催化作用
热门帖子
关注 科研通微信公众号,转发送积分 3784797
求助须知:如何正确求助?哪些是违规求助? 3330056
关于积分的说明 10244208
捐赠科研通 3045404
什么是DOI,文献DOI怎么找? 1671660
邀请新用户注册赠送积分活动 800577
科研通“疑难数据库(出版商)”最低求助积分说明 759508