# Evaluation of six clinical prognostic scores in NSCLC patients undergoing first line chemoimmunotherapy

**Authors:** Jiaqi Sun, Dan Li, Jiayin Liu, Lan Wang, Long Wang, Jing Han, Xue Zhang, Xinliang Zhou, Li Feng, Zhisong Fan, Jing Zuo, Yudong Wang

PMC · DOI: 10.3389/fimmu.2026.1695859 · Frontiers in Immunology · 2026-02-17

## TL;DR

This study compares six scoring systems to predict outcomes in non-small cell lung cancer patients treated with first-line chemoimmunotherapy.

## Contribution

The study evaluates and compares the performance of six clinical prognostic scores in the context of chemoimmunotherapy for NSCLC.

## Key findings

- The RMH score had the highest C-indices for both overall and progression-free survival.
- MDACC and MDACC+NLR also showed strong performance in predicting survival outcomes.
- Only MDACC remained statistically significant for overall survival after FDR correction.

## Abstract

The study aimed to evaluate the effectiveness of six prognostic scores for predicting the outcomes to first-line chemoimmunotherapy (CIT) in non-small cell lung cancer (NSCLC) patients.

NSCLC patients receiving first-line CIT were included. The prognostic scores evaluated were RMH, MDACC, MDACC+NLR, MDA-ICI, LIPI, and GRIm. Survival curves were generated using the Kaplan–Meier method, and univariate and multivariate analyses were conducted via the Cox proportional hazards regression model. The C−index and time−dependent AUC were calculated to comprehensively quantify and compare the predictive performance of each system. The Log−rank test and False Discovery Rate (FDR) correction was employed to compare survival outcomes across different risk groups defined by the six prognostic scoring systems.

A cohort of 298 NSCLC patients was analyzed. The median overall survival (mOS) of patients receiving first-line CIT was 36.5 months (95%CI: NE-NE), and the median progression-free survival (mPFS) was 14.5 months (95%CI: 11.9-17.1). Multivariate analysis showed that bone metastasis (P = 0.042), and more than two metastatic sites (P = 0.031) as independent predictors of poor OS. In quantitative performance comparison, RMH achieved the highest C-indices for both OS (0.672, 95%CI: 0.531-0.813) and PFS (0.652, 0.564-0.737); MDACC also performed well, with C-indices for OS (0.651, 0.564-0.737) and PFS (0.615, 0.554-0.738). Time-dependent AUC analysis showed that MDA-ICI attained the highest 1-year OS and PFS AUC (0.630 and 0.592), followed by the MDACC+NLR (0.600 and 0.571). Based on log-rank testing and following FDR correction, only the MDACC maintained a statistically significant association with OS (high-risk 14.0 vs. intermediate-risk 34.6 vs. low-risk NR months; P = 0.003, Q = 0.036). For PFS, the MDACC+NLR score showed a marginal significance after FDR correction (Q = 0.054).

The RMH, MDACC, and MDACC+NLR scoring systems all demonstrate prognostic utility in the NSCLC patients treated with first-line CIT, and the optimal choice among them may depend on the specific clinical context and the outcome metric of primary interest.

## Linked entities

- **Diseases:** non-small cell lung cancer (MONDO:0005233)

## Full-text entities

- **Genes:** CD274 (CD274 molecule) [NCBI Gene 29126] {aka ADMIO5, B7-H, B7H1, PD-L1, PDCD1L1, PDCD1LG1}, EGFR (epidermal growth factor receptor) [NCBI Gene 1956] {aka ERBB, ERBB1, ERRP, HER1, NISBD2, NNCIS}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, ALK (ALK receptor tyrosine kinase) [NCBI Gene 238] {aka ALK1, CD246, NBLST3}, ROS1 (ROS proto-oncogene 1, receptor tyrosine kinase) [NCBI Gene 6098] {aka MCF3, ROS, c-ros-1}, RET (ret proto-oncogene) [NCBI Gene 5979] {aka CDHF12, CDHR16, HSCR1, MEN2A, MEN2B, MTC1}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, LIPI (lipase I) [NCBI Gene 149998] {aka CT17, LPDL, PLA1C, PRED5, mPA-PLA1 beta}, ERBB2 (erb-b2 receptor tyrosine kinase 2) [NCBI Gene 2064] {aka CD340, HER-2, HER-2/neu, HER2, MLN 19, MLN-19}, MET (MET proto-oncogene, receptor tyrosine kinase) [NCBI Gene 4233] {aka AUTS9, DA11, DFNB97, HGFR, RCCP2, c-Met}, SPATA2 (spermatogenesis associated 2) [NCBI Gene 9825] {aka PD1, PPP1R145, tamo}
- **Diseases:** adenosquamous carcinoma (MESH:D018196), gastrointestinal tumor (MESH:D005770), kidneys (MESH:D007674), toxicity (MESH:D064420), cardiovascular or cerebrovascular diseases (MESH:D002318), infection (MESH:D007239), death (MESH:D003643), mOS (MESH:D011475), bone metastasis (MESH:D009362), non-squamous cell carcinoma (MESH:D002294), NSCLC (MESH:D002289), RMH (MESH:C536024), dysfunction of major organs (MESH:D009102), autoimmune disease (MESH:D001327), undifferentiated carcinoma (MESH:D002277), Lung cancer (MESH:D008175), SD (MESH:D012735), MDACC (MESH:D009369), adenocarcinoma (MESH:D000230), PD (MESH:D010300), NLR (MESH:D015467)
- **Chemicals:** nivolumab (MESH:D000077594), gemcitabine (MESH:D000093542), sintilimab (MESH:C000632826), taxanes (MESH:D043823), durvalumab (MESH:C000613593), Camrelizumab (MESH:C000631724), pembrolizumab (MESH:C582435), CIT (-), pemetrexed (MESH:D000068437), bevacizumab (MESH:D000068258), tislelizumab (MESH:C000707970), toripalimab (MESH:C000656314), MDA (MESH:D015104), platinum (MESH:D010984)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

31 references — full list in the complete paper: https://tomesphere.com/paper/PMC12953529/full.md

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Source: https://tomesphere.com/paper/PMC12953529