An online clinical model and risk stratification system to predict progression-free survival for advanced non-small-cell lung cancer patients treated with PD-(L)1 inhibitor

被引:0
|
作者
Tu, Zegui [1 ,2 ,3 ]
Yu, Yang [1 ,2 ]
Tian, Tian [1 ,2 ,3 ]
Li, Caili [4 ]
Luo, Jieyan [5 ]
机构
[1] Sichuan Univ, Div Thorac Tumor Multimodal Treatment, Chengdu 610041, Sichuan, Peoples R China
[2] Sichuan Univ, West China Hosp, Canc Ctr, Dept Med Oncol, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, West China Sch Med, Chengdu 610041, Sichuan, Peoples R China
[4] Sichuan Univ, West China Hosp, Day Surg Ctr, Gen Practice Med Ctr, Chengdu, Peoples R China
[5] Sichuan Univ, Peoples Hosp Ziyang 1, Ziyang Hosp, West China Hosp,Dept Oncol, Ziyang, Peoples R China
关键词
Non-small-cell lung cancer; Risk assessment; Progression-free survival; PD-(L)1 inhibitor; Immunotherapy; IMMUNE CHECKPOINT INHIBITORS; PD-1; BLOCKADE; NIVOLUMAB; IMMUNOTHERAPY; BIOMARKERS; DOCETAXEL;
D O I
10.1016/j.heliyon.2023.e20465
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background: Our study aimed to build a risk stratification system predicting the progression-free survival (PFS) to classify patients into diverse prognostic subgroups for advanced non-small-cell lung cancer patients treated with PD-(L)1 inhibitor. Methods: 404 patients from our center were enrolled in this study and 70% patients (n=282) were randomly assigned into the training cohort and other 30% patients (n=122) into the validation cohort. A testing cohort contained 81 patients from other centers were used to assess the generalizability of model. Cox regression analyses were used to identify the most significant clinical parameters. The model's performance was assessed by using concordance index (C- index), calibration curves, Decision Curve Analyses (DCAs), net reclassification improvement (NRI), integrated discrimination improvement (IDI) analyses, and survival curve. Results: Five clinical parameters were identified as the most significant predictors by using cox regression. We then integrated them into a Nomogram to Evaluate the relative PFS of ICIs Treatment (NEPIT). The C-index of NEPIT in the training cohort, the validation cohort and testing cohort was 0.789 (95%CI: 0.750-0.828), 0.745 (95%CI: 0.706-0.784), and 0.766 (95%CI: 0.744-0.788), respectively. The calibration curves presented a good congruence between the predictions and actual observations. The Decision Curve Analyses (DCAs) reflected positive net benefits can be obtained for NEPIT. The results from NRI and IDI analyses showed that the NEPIT could improve predictive power of TPS. In addition, the further constructed risk stratification system could effectively categorize patients into different risk subgroups. Conclusion: The tools developed in this study would have value in guiding the optimal patient selection for precision care.
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页数:11
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