Effects of Early Short-Course Corticosteroids on Immune-Related Adverse Events in Non-Small Cell Lung Cancer Patients Receiving Immune Checkpoint Inhibitors.

IF 2.5 3区 医学 Q3 ONCOLOGY
Oncology Pub Date : 2024-01-01 Epub Date: 2023-09-29 DOI:10.1159/000534350
Derek De-Rui Huang, Bin-Chi Liao, Wei-Hsun Hsu, Ching-Yao Yang, Yen-Ting Lin, Shang-Gin Wu, Tzu-Hsiu Tsai, Kuan-Yu Chen, Chao-Chi Ho, Wei-Yu Liao, Jin-Yuan Shih, Chong-Jen Yu, James Chih-Hsin Yang, Ann-Lii Cheng, Ying-Chun Shen
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引用次数: 0

Abstract

Introduction: In real-world practice, most non-small cell lung cancer (NSCLC) patients receiving combined immunochemotherapy are exposed to short-course corticosteroids following immune checkpoint inhibitor (ICI) infusion to prevent chemotherapy-related adverse events. However, whether this early short-course corticosteroid use prevents immune-related adverse events (irAEs) remains unknown.

Methods: Between January 1st, 2015, and December 31st, 2020, NSCLC patients who received at least one cycle of ICI with or without chemotherapy were enrolled. Early short-course corticosteroids were defined as corticosteroids administered following ICI injection and before chemotherapy on the same day and no longer than 3 days afterward. The patients were categorized as either "corticosteroid group" or "non-corticosteroid group" depending on their exposure to early short-course corticosteroid. The frequencies of irAEs requiring systemic corticosteroid use and irAEs leading to ICI discontinuation were compared between the two groups, and exploratory survival analyses were performed.

Results: Among 252 eligible patients, 137 patients were categorized as "corticosteroid group" and 115 patients as "non-corticosteroid group." The corticosteroid group enriched patients in the first-line setting (n = 75, 54.7%), compared to the non-corticosteroid group (n = 28, 24.3%). Thirty patients (21.9%) in the corticosteroid group and 35 patients (30.4%) in the non-corticosteroid group developed irAEs requiring systemic corticosteroid use (odds ratio [OR], 0.64; 95% confidence interval [CI], 0.35-1.18; p = 0.15). Eight patients (5.8%) in the corticosteroid group, as compared with 18 patients (15.7%) in the non-corticosteroid group, permanently discontinued ICI due to irAEs (OR, 0.34; 95% CI, 0.12-0.85; p = 0.013).

Conclusion: Early short-course corticosteroids following each ICI injection may reduce the rate of irAEs that lead to ICIs discontinuation, warranting further investigation of its prophylactic use to mitigate clinically significant irAEs.

早期短程皮质类固醇对接受免疫检查点抑制剂的非小细胞肺癌癌症患者免疫相关不良事件的影响。
简介:在现实生活中,大多数接受联合免疫化疗的非小细胞肺癌(NSCLC)患者在输注免疫检查点抑制剂(ICI)后暴露于短期皮质类固醇,以预防化疗相关的不良事件。然而,这种早期短期皮质类固醇的使用是否能预防免疫相关不良事件(irAE)仍不得而知。方法:在2015年1月1日至2020年12月31日期间,纳入至少接受一个周期ICI(包括或不包括化疗)的NSCLC患者。早期短期皮质类固醇被定义为在ICI注射后和化疗前在同一天且不超过3天后给予的皮质类固醇。根据患者在用药前接触皮质类固醇的情况,将其分为“皮质类固醇组”或“非皮质类固醇组。比较两组需要全身使用皮质类固醇的irAE和导致ICI停药的irAE的频率,并进行探索性生存分析。结果:在252名符合条件的患者中,137名患者被归类为“皮质类固醇组”,115名患者被分类为“非皮质类固醇组。皮质类固醇组在一线环境中富集患者(n=75、54.7%),与非皮质类固醇组相比(n=28,24.3%)。皮质类固醇组有30名患者(21.9%)和非皮质类固醇群组有35名患者(30.4%)出现需要全身使用皮质类固醇的irAE(比值比[OR],0.64;95%置信区间[CI],0.35至1.18;p=0.15),与非皮质类固醇组的18名患者(15.7%)相比,因irAE而永久停止ICI(OR,0.34;95%CI,0.12至0.85;p=0.013)。
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来源期刊
Oncology
Oncology 医学-肿瘤学
CiteScore
6.00
自引率
2.90%
发文量
76
审稿时长
6-12 weeks
期刊介绍: Although laboratory and clinical cancer research need to be closely linked, observations at the basic level often remain removed from medical applications. This journal works to accelerate the translation of experimental results into the clinic, and back again into the laboratory for further investigation. The fundamental purpose of this effort is to advance clinically-relevant knowledge of cancer, and improve the outcome of prevention, diagnosis and treatment of malignant disease. The journal publishes significant clinical studies from cancer programs around the world, along with important translational laboratory findings, mini-reviews (invited and submitted) and in-depth discussions of evolving and controversial topics in the oncology arena. A unique feature of the journal is a new section which focuses on rapid peer-review and subsequent publication of short reports of phase 1 and phase 2 clinical cancer trials, with a goal of insuring that high-quality clinical cancer research quickly enters the public domain, regardless of the trial’s ultimate conclusions regarding efficacy or toxicity.
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