Comparison of different criteria for estimating major pathological response in resectable non-small cell lung cancer treated with neoadjuvant chemoimmunotherapy

化学免疫疗法 病态的 医学 肺癌 临床终点 癌症 队列 肿瘤科 内科学 临床试验 免疫疗法
作者
Wei Sun,Xinying Liu,Chenglong Wang,Yumeng Jiang,Dongmei Lin
出处
期刊:Annals of Diagnostic Pathology [Elsevier BV]
卷期号:69: 152268-152268
标识
DOI:10.1016/j.anndiagpath.2024.152268
摘要

Major pathological response (MPR) is proposed as a surrogate endpoint for survival in non-small cell lung cancer (NSCLC) after neoadjuvant chemoimmunotherapy. However, the criteria for estimating MPR differ between the recommendations of the International Association for the Study of Lung Cancer (IASLC) and the immune-related pathologic response criterion (irPRC). IASLC's criteria focus solely on evaluating the primary tumor, while irPRC's criteria encompass both the primary tumor and lymph node metastasis. Our objective is to compare the prognostic value of different criteria for estimating MPR. We conducted a retrospective study on a cohort of 235 patients with NSCLC after neoadjuvant chemoimmunotherapy. The survival endpoint was event-free survival (EFS). The MPR status of each patient was evaluated using both IASLC's criteria and irPRC's criteria. The prognostic value was compared using the Area Under Curve (AUC). The MPR rates were 63.4 % (149/235) and 57.4 % (135/235) according to IASLC's and irPRC's criteria, respectively. Inconsistent cases, characterized by MPR status according to IASLC's criteria but non-MPR status according to irPRC's criteria, constituted 6.0 % (14/235) of the overall cohort and 15.2 % (14/92) of patients with pretreatment N positive disease. Interestingly, all inconsistent patients showed no recurrence during the study period. Although both MPR statuses according to IASLC (p = 0.00039) and irPRC (p = 0.0094) were associated with improved EFS, IASLC's criteria (AUC = 0.65) were superior to irPRC's criteria (AUC = 0.62) with a higher AUC value. IASLC's criteria for estimating MPR were superior to irPRC's criteria in predicting EFS for NSCLC after neoadjuvant chemoimmunotherapy.
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
传奇3应助Elielieli采纳,获得10
刚刚
1秒前
欢喜的小天鹅完成签到 ,获得积分10
1秒前
莫里完成签到,获得积分10
1秒前
zhoucheng完成签到,获得积分10
2秒前
aaawen发布了新的文献求助10
2秒前
2秒前
书虫发布了新的文献求助10
3秒前
机灵忆安完成签到,获得积分10
3秒前
岩松完成签到 ,获得积分10
4秒前
Jenlisa完成签到 ,获得积分10
4秒前
4秒前
139完成签到 ,获得积分0
4秒前
褚晣完成签到,获得积分10
4秒前
taster完成签到,获得积分10
5秒前
柯友卉完成签到 ,获得积分10
5秒前
一枝完成签到 ,获得积分10
5秒前
田様应助听说外面下雨了采纳,获得10
5秒前
俞禛发布了新的文献求助10
6秒前
VvV完成签到,获得积分10
6秒前
chiaoyin999发布了新的文献求助20
6秒前
wanci应助LL采纳,获得10
6秒前
Azlne完成签到 ,获得积分10
7秒前
7秒前
子寒完成签到,获得积分10
7秒前
whale完成签到,获得积分10
7秒前
cdercder应助小沐采纳,获得10
7秒前
8秒前
搜集达人应助bjbbh采纳,获得30
8秒前
妮妮爱smile完成签到,获得积分10
8秒前
why完成签到 ,获得积分10
8秒前
xuxingjie完成签到,获得积分10
8秒前
大方念云完成签到,获得积分10
8秒前
下雨收衣服完成签到,获得积分10
9秒前
丘比特应助今夜无人入眠采纳,获得10
10秒前
wansida完成签到,获得积分10
10秒前
10秒前
纪间完成签到,获得积分10
11秒前
Wjh123456完成签到,获得积分10
11秒前
pcr163应助whatever采纳,获得100
12秒前
高分求助中
Applied Survey Data Analysis (第三版, 2025) 800
Assessing and Diagnosing Young Children with Neurodevelopmental Disorders (2nd Edition) 700
Images that translate 500
引进保护装置的分析评价八七年国外进口线路等保护运行情况介绍 500
Algorithmic Mathematics in Machine Learning 500
Handbook of Innovations in Political Psychology 400
Mapping the Stars: Celebrity, Metonymy, and the Networked Politics of Identity 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 3841198
求助须知:如何正确求助?哪些是违规求助? 3383176
关于积分的说明 10528587
捐赠科研通 3103166
什么是DOI,文献DOI怎么找? 1709180
邀请新用户注册赠送积分活动 822971
科研通“疑难数据库(出版商)”最低求助积分说明 773733