Efficacy and safety of combining radiotherapy with immune checkpoint inhibitors in patients with advanced non-small cell lung cancer: a real-world study.

IF 2.9 4区 医学 Q3 IMMUNOLOGY
Guanli Yang, Zhen Zhou, Chengxin Liu
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引用次数: 0

Abstract

Background: The significance of local radiotherapy (RT) in advanced non-small-cell lung cancer (NSCLC) is well documented. However, the advent of immunotherapy has raised questions regarding the synergistic survival benefits or potential adverse effects.

Objective: This study aimed to explore whether a combination of RT and systematic immune checkpoint inhibitors (ICIs) can improve the survival outcomes for NSCLC patients.

Methods: Based on collected data patients who received RT were defined as the RT group, and those who had not for any site were defined as the non-RT group. Propensity score matching (PSM) was employed to mitigate bias. The primary endpoint was progression-free survival (PFS), with secondary endpoints including overall survival (OS) and treatment-related adverse events (AEs).

Results: Out of 709 patients (235 in RT group and 474 in non-RT group) were included, with 213 patients per group. The median PFS of the RT group was better than that of the non-RT group (13.8 months versus 9.5 months; p < 0.0001), although no superiority in median overall survival (OS) of the RT group was observed (p = 0.715). However, among the cohort of patients with ≤3 metastases, the median OS of the RT group improved significantly (HR = 0.60, [95% CI 0.44-0.83]; p = 0.004). Treatment-related AEs occurred in 94.5% of RT group patients and in 94.9% of non-RT group patients (p = 0.792), which indicated no observable increase in AEs from RT.

Conclusions: These results demonstrate the tolerability of RT when administered along with immunotherapy, suggesting its potential to positively impact the survival outcomes of NSCLC patients.

晚期非小细胞肺癌患者联合放疗与免疫检查点抑制剂的疗效与安全性:一项真实世界研究。
背景:晚期非小细胞肺癌(NSCLC)局部放疗(RT)的重要性有据可查。然而,免疫疗法的出现引发了有关协同生存益处或潜在不良反应的问题:本研究旨在探讨 RT 与系统性免疫检查点抑制剂(ICIs)的联合应用能否改善 NSCLC 患者的生存预后:根据收集的数据,将接受过RT治疗的患者定义为RT组,未接受过任何部位RT治疗的患者定义为非RT组。采用倾向评分匹配(PSM)来减少偏倚。主要终点为无进展生存期(PFS),次要终点包括总生存期(OS)和治疗相关不良事件(AEs):共纳入 709 例患者(RT 组 235 例,非 RT 组 474 例),每组 213 例。RT 组的中位生存期优于非 RT 组(13.8 个月对 9.5 个月;P = 0.715)。然而,在转移灶≤3个的患者队列中,RT组的中位OS显著改善(HR = 0.60,[95% CI 0.44-0.83];P = 0.004)。94.5%的RT组患者和94.9%的非RT组患者出现了治疗相关的AEs(p = 0.792),这表明RT引起的AEs没有明显增加:这些结果表明,RT 在与免疫疗法同时使用时具有耐受性,表明其有可能对 NSCLC 患者的生存结果产生积极影响。
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来源期刊
CiteScore
5.40
自引率
0.00%
发文量
133
审稿时长
4-8 weeks
期刊介绍: The journal Immunopharmacology and Immunotoxicology is devoted to pre-clinical and clinical drug discovery and development targeting the immune system. Research related to the immunoregulatory effects of various compounds, including small-molecule drugs and biologics, on immunocompetent cells and immune responses, as well as the immunotoxicity exerted by xenobiotics and drugs. Only research that describe the mechanisms of specific compounds (not extracts) is of interest to the journal. The journal will prioritise preclinical and clinical studies on immunotherapy of disorders such as chronic inflammation, allergy, autoimmunity, cancer etc. The effects of small-drugs, vaccines and biologics against central immunological targets as well as cell-based therapy, including dendritic cell therapy, T cell adoptive transfer and stem cell therapy, are topics of particular interest. Publications pointing towards potential new drug targets within the immune system or novel technology for immunopharmacological drug development are also welcome. With an immunoscience focus on drug development, immunotherapy and toxicology, the journal will cover areas such as infection, allergy, inflammation, tumor immunology, degenerative disorders, immunodeficiencies, neurology, atherosclerosis and more. Immunopharmacology and Immunotoxicology will accept original manuscripts, brief communications, commentaries, mini-reviews, reviews, clinical trials and clinical cases, on the condition that the results reported are based on original, clinical, or basic research that has not been published elsewhere in any journal in any language (except in abstract form relating to paper communicated to scientific meetings and symposiums).
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