Impact of corticosteroids on the efficacy of first-line pembrolizumab plus chemotherapy in patients with advanced non-small-cell lung cancer.

IF 4.2 2区 医学 Q2 ONCOLOGY Therapeutic Advances in Medical Oncology Pub Date : 2025-02-11 eCollection Date: 2025-01-01 DOI:10.1177/17588359251318160
Amytis Roboubi, Eric Wasielewski, Soraya Bordier, Amélie Turlotte, Geoffrey Pavaut, Arnaud Scherpereel, Alexis Cortot, Clément Gauvain
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Abstract

Background: Systemic corticosteroids (SCs) are associated with reduced survival in patients with advanced non-small-cell lung cancer (NSCLC) receiving immune checkpoint inhibitor (ICI) monotherapy. However, the current first-line standard of care usually involves combined chemotherapy (CT) and ICIs, and the effect of SCs on survival under combined CT and ICI has never been studied.

Objectives: To investigate the association between SC therapy and survival under CT-ICI in advanced-stage NSCLC patients.

Design: We performed a multicenter retrospective cohort study of all advanced-stage NSCLC patients receiving first-line CT-ICI.

Methods: The primary endpoint was progression-free survival (PFS) according to SC exposure status (⩾10 mg/day), adjusted in a multivariate Cox model for the following confounders: age, performance status, hospital admission prior to treatment, number of metastatic sites, brain metastases, bone metastases, PD-L1 status, and histological subtype. Multivariate analyses also explored the association between dosage and SC exposure duration and PFS.

Results: Of the 193 included patients, 43 (22.3%) were receiving SCs, mainly because of symptomatic brain metastases (in 25/43 cases, 58%). In multivariate analysis, SC therapy at a 10 mg/day threshold was not associated with PFS (hazard ratio (HR) = 1.25, 95% confidence interval (CI) 0.77-2.03, p = 0.35). However, SC dose was negatively associated with PFS (HR = 1.08 per 10 mg/day increment, 95% CI 1.01-1.16, p = 0.01) especially at doses ⩾60 mg/day (HR = 3.27 per 10 mg/day increment, 95% CI 2.01-5.35, p < 0.001). Duration of SC therapy was not associated with PFS (HR = 0.97, 95% CI 0.81-1.15, p = 0.71), but SC therapy ⩾4 weeks prior to CT-ICI was associated with shorter PFS (HR = 1.07, 95% CI: 1.01-1.14, p = 0.028).

Conclusion: In this group of patients receiving first-line CT-ICI for advanced NSCLC, SCs at ⩾60 mg/day were associated with shorter PFS, but lower doses were not. Prolonged SC therapy prior to CT-ICI was associated with shorter PFS. Larger studies are required to confirm these results.

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皮质类固醇对晚期非小细胞肺癌患者一线派姆单抗加化疗疗效的影响
背景:在接受免疫检查点抑制剂(ICI)单药治疗的晚期非小细胞肺癌(NSCLC)患者中,全身性皮质类固醇(SCs)与生存率降低相关。然而,目前的一线治疗标准通常包括联合化疗(CT)和ICIs,而SCs对CT和ICI联合下生存的影响尚未研究。目的:探讨SC治疗与晚期NSCLC患者CT-ICI存活之间的关系。设计:我们对所有接受一线CT-ICI治疗的晚期非小细胞肺癌患者进行了一项多中心回顾性队列研究。方法:主要终点是根据SC暴露状态(大于或小于10 mg/天)的无进展生存期(PFS),在针对以下混杂因素的多变量Cox模型中进行调整:年龄、表现状态、治疗前住院、转移部位数量、脑转移、骨转移、PD-L1状态和组织学亚型。多变量分析还探讨了剂量和SC暴露时间与PFS之间的关系。结果:在193例纳入的患者中,43例(22.3%)接受了SCs,主要是因为有症状的脑转移(25/43例,58%)。在多变量分析中,10mg /天阈值的SC治疗与PFS无关(风险比(HR) = 1.25, 95%可信区间(CI) 0.77-2.03, p = 0.35)。然而,SC剂量与PFS呈负相关(HR = 1.08每10 mg/天增量,95% CI 1.01-1.16, p = 0.01),特别是在剂量大于或等于60 mg/天时(HR = 3.27每10 mg/天增量,95% CI 2.01-5.35, p = 0.71),但是在CT-ICI之前小于或等于4周的SC治疗与较短的PFS相关(HR = 1.07, 95% CI: 1.01-1.14, p = 0.028)。结论:在这组接受一线CT-ICI治疗晚期NSCLC的患者中,大于或等于60 mg/天的SCs与较短的PFS相关,但较低剂量则不然。在CT-ICI之前延长SC治疗与较短的PFS相关。需要更大规模的研究来证实这些结果。
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来源期刊
CiteScore
8.20
自引率
2.00%
发文量
160
审稿时长
15 weeks
期刊介绍: Therapeutic Advances in Medical Oncology is an open access, peer-reviewed journal delivering the highest quality articles, reviews, and scholarly comment on pioneering efforts and innovative studies in the medical treatment of cancer. The journal has a strong clinical and pharmacological focus and is aimed at clinicians and researchers in medical oncology, providing a forum in print and online for publishing the highest quality articles in this area. This journal is a member of the Committee on Publication Ethics (COPE).
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