医学
免疫疗法
单变量
内科学
对数秩检验
进行性疾病
肿瘤科
单变量分析
疾病
性能状态
多元分析
生存分析
癌症
多元统计
机器学习
计算机科学
作者
Younes Belkouchi,Hugues Talbot,Nathalie Lassau,Littisha Lawrance,Siham Farhane,Rahma Feki-Mkaouar,Joya Hadchiti,Lama Dawi,Julien Vibert,Paul-Henry Cournède,Clara Cousteix,Camille Mazza,Michèle Kind,Antoîne Italiano,Aurélien Marabelle,Samy Ammari,Stéphane Champiat
标识
DOI:10.1158/1078-0432.ccr-22-0890
摘要
The objective of the study is to propose the immunotherapy progression decision (iPD) score, a practical tool based on patient features that are available at the first evaluation of immunotherapy treatment, to help oncologists decide whether to continue the treatment or switch rapidly to another therapeutic line when facing a progressive disease patient at the first evaluation.This retrospective study included 107 patients with progressive disease at first evaluation according to RECIST 1.1. Clinical, radiological, and biological data at baseline and first evaluation were analyzed. An external validation set consisting of 31 patients with similar baseline characteristics was used for the validation of the score.Variables were analyzed in a univariate study. The iPD score was constructed using only independent variables, each considered as a worsening factor for the survival of patients. The patients were stratified in three groups: good prognosis (GP), poor prognosis (PP), and critical prognosis (CP). Each group showed significantly different survivals (GP: 11.4, PP: 4.4, CP: 2.3 months median overall survival, P < 0.001, log-rank test). Moreover, the iPD score was able to detect the pseudoprogressors better than other scores. On the validation set, CP patients had significantly worse survival than PP and GP patients (P < 0.05, log-rank test).The iPD score provides oncologists with a new evaluation, computable at first progression, to decide whether treatment should be continued (for the GP group), or immediately changed for the PP and CP groups. Further validation on larger cohorts is needed to prove its efficacy in clinical practice.
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