Real-world comparison of chemo-immunotherapy and chemotherapy alone in the treatment of extensive-stage small-cell lung cancer

IF 2.2 4区 医学 Q3 RESPIRATORY SYSTEM Respiratory Medicine and Research Pub Date : 2024-07-01 DOI:10.1016/j.resmer.2024.101125
D. Lamy , P. Mouillot , A. Mariet , R. Barnestein , F. Quilot , C. Fraisse , F. Ghiringhelli , P. Bonniaud , A. Zouak , P. Foucher
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Abstract

Introduction

Small cell lung cancer (SCLC) is a high-grade neuroendocrine carcinoma responsible for 200,000 deaths per year worldwide. Platinum-etoposide-based chemotherapy has been the standard of treatment for the past 40 years, with an overall survival of 10 months. Since 2019, the addition of immunotherapy (atezolizumab or durvalumab) to chemotherapy has become the standard of care for first-line treatment of extensive-stage SCLC following the demonstration of an improvement in overall survival in phase 3 studies. We aimed to evaluate the efficacy and safety of chemo-immunotherapy compared with chemotherapy alone in a “real-world” setting.

Methods

Retrospective observational study including patients undergoing first-line treatment for extensive-stage SCLC between 2014 and 2022. We separated the study population into two arms (chemo-immunotherapy/chemotherapy). For each arm, progression-free survival (PFS), overall survival (OS) and serious side effects were collected. Associations between treatments and survival outcomes were adjusted for potential confounders. Consolidative palliative thoracic radiotherapy was introduced in the models as a time-dependent variable.

Results

A total of 118 patients with a median age of 63 years were included. 65.2 % of patients were performance status 0 or 1. In univariate analysis, PFS and OS were not significantly different between the chemo-immunotherapy and chemotherapy alone groups (p = 0.70 and 0.24 respectively). In multivariate analysis, the addition of immunotherapy to chemotherapy was not significantly associated with better PFS (HR 0.76, IC (0.49 – 1.19), p = 0.23), but it was significantly associated with better OS (HR 0.61, IC (0.38 – 0.98), p = 0.04). Consolidative palliative thoracic radiotherapy (time-dependent variable), when applied (almost only in the chemotherapy alone group), was significantly associated with better PFS and OS.

Discussion

In this real-world study, chemo-immunotherapy was associated with slightly better OS compared to chemotherapy alone as a first-line treatment in ES-SCLC patients in multivariate analysis, which is not explained by a benefit in PFS. However, consolidative palliative thoracic radiotherapy seems to be significantly associated with better OS and PFS, suggesting that we should also consider using it in patients receiving chemo-immunotherapy.

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化疗-免疫疗法与单纯化疗治疗广泛期小细胞肺癌的真实世界比较
导言小细胞肺癌(SCLC)是一种高级别神经内分泌癌,全世界每年有 20 万人死于这种癌症。过去40年来,以铂-依托泊苷为基础的化疗一直是标准治疗方法,总生存期为10个月。自2019年以来,在化疗基础上加用免疫疗法(atezolizumab或durvalumab)已成为广泛期SCLC一线治疗的标准疗法,因为在3期研究中总生存期得到了改善。我们的目的是在 "真实世界 "环境中评估化疗免疫疗法与单纯化疗相比的疗效和安全性。方法回顾性观察研究包括2014年至2022年间接受广泛期SCLC一线治疗的患者。我们将研究对象分为两组(化疗-免疫治疗/化疗)。我们收集了每个治疗组的无进展生存期(PFS)、总生存期(OS)和严重副作用。对潜在的混杂因素调整了治疗与生存结果之间的关联。综合姑息胸腔放疗作为时间变量被引入模型中。65.2%的患者表现为 0 或 1。在单变量分析中,化疗-免疫治疗组和单纯化疗组的生存期和手术时间无明显差异(P = 0.70 和 0.24)。在多变量分析中,在化疗基础上加用免疫疗法与更好的PFS无明显相关性(HR 0.76,IC (0.49 - 1.19),p = 0.23),但与更好的OS有明显相关性(HR 0.61,IC (0.38 - 0.98),p = 0.04)。讨论在这项真实世界的研究中,与单纯化疗相比,化疗免疫疗法作为ES-SCLC患者一线治疗的多变量分析结果显示,化疗免疫疗法的OS略好于单纯化疗,但PFS的获益并不能解释这一点。然而,巩固性姑息胸腔放疗似乎与更好的OS和PFS显著相关,这表明我们也应考虑在接受化疗免疫治疗的患者中使用这种疗法。
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来源期刊
Respiratory Medicine and Research
Respiratory Medicine and Research RESPIRATORY SYSTEM-
CiteScore
2.70
自引率
0.00%
发文量
82
审稿时长
50 days
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