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

IF 2.3 3区 医学 Q3 ONCOLOGY
Thoracic Cancer Pub Date : 2024-08-01 Epub Date: 2024-07-19 DOI:10.1111/1759-7714.15401
I M Horstman, P C Vinke, E Suazo-Zepeda, T J N Hiltermann, M A Heuvelmans, E Corpeleijn, G H de Bock
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引用次数: 0

Abstract

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.

接受免疫检查点抑制剂治疗的非小细胞肺癌患者的营养和炎症生物标志物与总生存期的关系。
目的:需要用治疗前生物标志物来识别生存率可能较低的非小细胞肺癌(NSCLC)患者。这样才能确保只有真正有机会获益的患者才能接受免疫检查点抑制剂(ICI)治疗。在这项研究中,我们研究了接受 ICIs 治疗的 NSCLC 患者真实世界队列中基线营养和炎症生物标志物与总生存期的关系:我们使用了从OncoLifeS数据生物库中收集的前瞻性数据。该队列包括 500 名在 2015 年 5 月至 2021 年 6 月期间接受 ICIs 治疗的晚期 NSCLC 患者。对ICI治疗前2周内的生物标志物进行了评估:中性粒细胞与淋巴细胞比值、C反应蛋白(CRP)、格拉斯哥预后评分、CRP/白蛋白比值(CAR)、预后营养指数(PNI)和晚期肺癌炎症指数。对于每种生物标志物,均采用基于文献的临界值来定义低风险组和高风险组。利用调整后生存分析估算出调整后危险比(aHRs)和95%置信区间(95% CIs):大多数患者为男性(60.8%),平均基线年龄为 65 ± 9 岁,88% 的患者为 IV 期疾病。就每种生物标志物而言,低风险患者的总生存率都较高(全部,P 结论:这些结果突显了营养保健的潜在价值:这些结果凸显了营养和炎症生物标志物(尤其是 CAR 和 PNI)在开始 ICI 治疗前识别死亡风险最高的 NSCLC 患者方面的潜在价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Thoracic Cancer
Thoracic Cancer ONCOLOGY-RESPIRATORY SYSTEM
CiteScore
5.20
自引率
3.40%
发文量
439
审稿时长
2 months
期刊介绍: Thoracic Cancer aims to facilitate international collaboration and exchange of comprehensive and cutting-edge information on basic, translational, and applied clinical research in lung cancer, esophageal cancer, mediastinal cancer, breast cancer and other thoracic malignancies. Prevention, treatment and research relevant to Asia-Pacific is a focus area, but submissions from all regions are welcomed. The editors encourage contributions relevant to prevention, general thoracic surgery, medical oncology, radiology, radiation medicine, pathology, basic cancer research, as well as epidemiological and translational studies in thoracic cancer. Thoracic Cancer is the official publication of the Chinese Society of Lung Cancer, International Chinese Society of Thoracic Surgery and is endorsed by the Korean Association for the Study of Lung Cancer and the Hong Kong Cancer Therapy Society. The Journal publishes a range of article types including: Editorials, Invited Reviews, Mini Reviews, Original Articles, Clinical Guidelines, Technological Notes, Imaging in thoracic cancer, Meeting Reports, Case Reports, Letters to the Editor, Commentaries, and Brief Reports.
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