The association of nutritional and inflammatory biomarkers with overall survival in patients with non-small-cell lung cancer treated with immune checkpoint inhibitors

被引:1
|
作者
Horstman, I. M. [1 ]
Vinke, P. C. [1 ]
Suazo-Zepeda, E. [1 ]
Hiltermann, T. J. N. [2 ]
Heuvelmans, M. A. [1 ]
Corpeleijn, E. [1 ]
de Bock, G. H. [1 ]
机构
[1] Univ Groningen, Univ Med Ctr Groningen, Dept Epidemiol, Groningen, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Pulmonol, Groningen, Netherlands
基金
欧盟地平线“2020”;
关键词
non-small-cell lung cancer; immunotherapy; immune checkpoint inhibitors; nutritional and inflammatory biomarkers; prognostic markers; GLASGOW PROGNOSTIC SCORE;
D O I
10.1111/1759-7714.15401
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Objectives: Pretreatment biomarkers are needed to identify patients with non-small-cell lung cancer (NSCLC) likely to have worse survival. This ensures that only patients with a real chance of benefit receive immune checkpoint inhibitor (ICI) treatment. In this study, we examined the associations of baseline nutritional and inflammatory biomarkers with overall survival in a real-world cohort of NSCLC patients who received ICIs. Materials and Methods: We used prospectively collected data from the OncoLifeS data biobank. The cohort included 500 advanced-stage NSCLC patients treated with ICIs from May 2015 to June 2021. Biomarkers were evaluated within 2 weeks before ICI treatment: neutrophil-to-lymphocyte ratio, C-reactive protein (CRP), Glasgow prognostic score, CRP/albumin ratio (CAR), prognostic nutritional index (PNI), and advanced lung cancer inflammation index. For each biomarker, low- and high-risk groups were defined using literature-based cut-offs. Adjusted hazard ratios (aHRs) and 95% confidence intervals (95% CIs) were estimated using adjusted survival analysis. Results: Most patients were male (60.8%), the mean baseline age was 65 +/- 9 years, and 88% had stage IV disease. For each biomarker, low-risk patients had better overall survival (all, p < 0.001), with CAR and PNI showing the strongest associations. In multivariable analyses a combined CAR/PNI risk score had a stronger association with overall survival (aHR 3.09, 95% CI 2.36-4.06) than CAR alone (aHR 2.22, 95% CI 1.79-2.76) or PNI alone (aHR 2.09, 95% CI 1.66-2.61). Conclusion: These results highlight the potential value of nutritional and inflammatory biomarkers, in particular CAR and PNI, in identifying NSCLC patients with highest mortality risk before starting ICI treatment.
引用
收藏
页码:1764 / 1771
页数:8
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