Application of immunotherapy in advanced non-small cell lung cancer with hypertension: a multicenter retrospective analysis.

IF 3.5 3区 医学 Q2 ONCOLOGY
Frontiers in Oncology Pub Date : 2025-09-12 eCollection Date: 2025-01-01 DOI:10.3389/fonc.2025.1621363
Jingyi Yuan, Kaixin Lei, Quanling Kong, Tao Chang, Xinhang Gu, Juan Wang, Li-Na He, Jiadi Gan, Bojiang Chen
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引用次数: 0

Abstract

Importance: Immune checkpoint inhibitors (ICIs) have become the standard treatment for advanced non-small cell lung cancer (NSCLC). However, their prognostic role in NSCLC patients remains controversial. Hypertension (HTN) is an important risk factor for many cancers, but the pathogenesis underlying HTN in relation to cancer prognosis remains unclear.

Objective: We aimed to investigate the possible association between HTN and prognosis in advanced NSCLC patients.

Data sources: Data on advanced NSCLC patients receiving immunotherapy at stages IIIb, IIIc or IV were included.

Study selection: Multicenter retrospective studies and trials reporting the use of immunotherapy were included. Main outcomes and measures: Progression-free survival (PFS) and overall survival (OS) were analyzed using Cox proportional hazards models and were estimated by the Kaplan-Meier method. Subgroup analysis on NSCLC hypertensive patients was pre-planned and was presented in the form of Forest Plot. Statistical software utilized for all analyses included statistical analysis system (SAS) V.9.4 and R version 4.2.2 (R Foundation for Statistical Computing).

Results: Between January 2016 and June 2024, 1175 NSCLC patients receiving immunotherapy were enrolled, with 219 (18.6%) classified as hypertensive group and 956 (81.4%) classified as non-hypertensive group. Neutrophil count and ECOG = 2 showed a significant association with OS in univariate analysis (HR = 0.69, 95%Cl: 0.51 - 0.92, P = 0.012, and HR = 1.02, 95%Cl: 1.00 to 1.03, P = 0.008 respectively). In multivariate analysis, ECOG = 2 was significantly correlated with OS (HR = 0.73, 95%Cl: 0.54 to 0.98, P = 0.037) and PD - 1/PD-L1 had significant association with PFS (HR = 1.27, 95%Cl: 1.00 to 1.61, P = 0.050). OS was found significantly longer in non-hypertensive group than in hypertensive group (P = 0.049). No baseline indicator was found significant correlated with the survival prognosis of patients receiving immunotherapy in subgroup analysis.

Conclusion and relevance: The non-hypertensive group was associated with a lower risk of mortality than hypertensive group. In subgroup analysis, no baseline indicator was observed a significant correlation with survival prognosis on OS and PFS in hypertensive patients. Our findings provided an important prognostic factor to improve the prognosis of advanced NSCLC patients receiving immunotherapy. Prospective randomized trials are needed to further validate these findings.

免疫治疗在晚期非小细胞肺癌合并高血压中的应用:一项多中心回顾性分析。
重要性:免疫检查点抑制剂(ICIs)已成为晚期非小细胞肺癌(NSCLC)的标准治疗。然而,它们在非小细胞肺癌患者中的预后作用仍存在争议。高血压(HTN)是许多癌症的重要危险因素,但HTN的发病机制与癌症预后的关系尚不清楚。目的:探讨HTN与晚期非小细胞肺癌患者预后的关系。数据来源:包括在IIIb、IIIc或IV期接受免疫治疗的晚期NSCLC患者的数据。研究选择:包括多中心回顾性研究和报告使用免疫疗法的试验。主要结局和测量指标:采用Cox比例风险模型分析无进展生存期(PFS)和总生存期(OS),并采用Kaplan-Meier方法进行估计。非小细胞肺癌高血压患者的亚组分析是预先计划的,并以森林图的形式呈现。所有分析使用的统计软件包括统计分析系统(SAS) V.9.4和R 4.2.2版本(R Foundation for Statistical Computing)。结果:2016年1月至2024年6月,共纳入接受免疫治疗的NSCLC患者1175例,其中高血压组219例(18.6%),非高血压组956例(81.4%)。单因素分析中,中性粒细胞计数和ECOG = 2与OS有显著相关性(HR = 0.69, 95%Cl: 0.51 ~ 0.92, P = 0.012; HR = 1.02, 95%Cl: 1.00 ~ 1.03, P = 0.008)。多因素分析中,ECOG = 2与OS显著相关(HR = 0.73, 95%Cl: 0.54 ~ 0.98, P = 0.037), PD- 1/PD- l1与PFS显著相关(HR = 1.27, 95%Cl: 1.00 ~ 1.61, P = 0.050)。非高血压组OS明显长于高血压组(P = 0.049)。亚组分析中未发现基线指标与接受免疫治疗患者的生存预后有显著相关性。结论及意义:非高血压组的死亡风险低于高血压组。在亚组分析中,没有发现基线指标与高血压患者OS和PFS的生存预后有显著相关性。我们的研究结果为改善晚期NSCLC患者接受免疫治疗的预后提供了一个重要的预后因素。需要前瞻性随机试验来进一步验证这些发现。
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
Frontiers in Oncology
Frontiers in Oncology Biochemistry, Genetics and Molecular Biology-Cancer Research
CiteScore
6.20
自引率
10.60%
发文量
6641
审稿时长
14 weeks
期刊介绍: Cancer Imaging and Diagnosis is dedicated to the publication of results from clinical and research studies applied to cancer diagnosis and treatment. The section aims to publish studies from the entire field of cancer imaging: results from routine use of clinical imaging in both radiology and nuclear medicine, results from clinical trials, experimental molecular imaging in humans and small animals, research on new contrast agents in CT, MRI, ultrasound, publication of new technical applications and processing algorithms to improve the standardization of quantitative imaging and image guided interventions for the diagnosis and treatment of cancer.
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