诱导化疗周期数对一线atezolizumab联合化疗治疗广泛期小细胞肺癌疗效的影响

IF 3.5 2区 医学 Q2 ONCOLOGY
Translational lung cancer research Pub Date : 2025-04-30 Epub Date: 2025-04-15 DOI:10.21037/tlcr-2025-207
Mengxing You, Jiayu Liu, Fei Teng, Lige Wu, Haifeng Qin, Yan Zhang, Cuiying Zhang, Ziling Liu, Kewei Ma, Esteban C Gabazza, Jacopo Vannucci, Xuezhi Hao, Junling Li, Puyuan Xing
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引用次数: 0

摘要

背景:与单纯化疗相比,广泛期小细胞肺癌(ES-SCLC)的一线治疗中加用atezolizumab可提高总生存期(OS),但获益仍然有限。本研究旨在探讨影响预后的因素,并评估诱导化疗周期数对治疗效果的影响。方法:我们回顾性分析了2020年3月至2022年9月期间在五个中心治疗的ES-SCLC患者的数据。所有45例患者均接受依托泊苷+铂联合atezolizumab的一线治疗。主要终点是基于诱导化疗周期数的总人群和亚人群的无进展生存期(PFS)和OS。采用最小绝对收缩和选择算子(LASSO)回归识别预后变量,并评估不同诱导化疗周期数对治疗效果的影响。结果:共有45例患者入组。一线治疗的中位PFS为7个月,中位OS为17.6个月。采用LASSO回归分析10个变量:性别、年龄、肝转移、骨转移、脑转移、一线诱导化疗周期数、一线免疫治疗维持、接受跨线免疫治疗、胸部放疗、脑放疗。分析发现,接受≥6个周期的诱导化疗是影响预后的最重要变量,也是唯一一个有统计学意义的变量[一致性指数:0.658;风险比:0.32(95%可信区间:0.17-0.63)。接受≥6个周期诱导化疗的患者(n=25)比接受诱导化疗的患者有更长的中位PFS(8个月对5个月)和中位OS(18.5个月对13.1个月)。结论:接受≥6个周期诱导化疗显著延长了患者的中位PFS和中位OS,突出了其影响一线atezolizumab联合化疗治疗ES-SCLC患者疗效的关键因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of the number of induction chemotherapy cycles on the efficacy of first-line atezolizumab combined with chemotherapy in extensive-stage small cell lung cancer.

Background: Compared with chemotherapy alone, the addition of atezolizumab to the first-line treatment of extensive-stage small cell lung cancer (ES-SCLC) improves the overall survival (OS), but the benefit remains limited. This study aims at investigating the factors influencing prognosis and to assess the effect of the number of induction chemotherapy cycles on treatment efficacy.

Methods: We retrospectively analyzed the data of patients with ES-SCLC treated in five centers between March 2020 and September 2022. All 45 patients received first-line treatment with etoposide plus platinum combined with atezolizumab. The primary endpoints were progression-free survival (PFS) and OS in the total population and subpopulations based on the number of induction chemotherapy cycles. Least absolute shrinkage and selection operator (LASSO) regression were applied to identify the prognostic variables, and the effect of varying the number of induction chemotherapy cycles on the treatment efficacy was evaluated.

Results: A total of 45 patients were enrolled in the study. The median PFS for the first-line treatment was 7 months, and the median OS was 17.6 months. The following 10 variables were analyzed using LASSO regression: gender, age, liver metastasis, bone metastasis, brain metastasis, number of first-line induction chemotherapy cycles, first-line immunotherapy maintenance, receipt of cross-line immunotherapy, chest radiotherapy, and brain radiotherapy. The analysis revealed that receiving ≥6 cycles of induction chemotherapy was the most important variable affecting prognosis and the only one significant [concordance index: 0.658; hazard ratio: 0.32 (95% confidence interval: 0.17-0.63)]. Patients who received ≥6 cycles of induction chemotherapy (n=25) had a longer median PFS (8 vs. 5 months) and median OS (18.5 vs. 13.1 months) than those who received <6 cycles (n=20). Subgroup analyses indicated consistent survival benefits of ≥6 induction chemotherapy cycles across key subgroups, including males, patients aged ≤65 years, and those with or without brain metastasis (all P value <0.05).

Conclusions: Receiving ≥6 cycles of induction chemotherapy significantly prolonged the median PFS and median OS of patients, highlighting its crucial factor influencing the efficacy of first-line atezolizumab combined with chemotherapy in patients with ES-SCLC.

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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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