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一线阿替利珠单抗联合化疗治疗广泛期小细胞肺癌的治疗持续时间的影响:一项多中心真实世界回顾性研究

Impact of Treatment Duration in First-Line Atezolizumab Plus Chemotherapy in Extensive-Stage Small-Cell Lung Cancer: A Multicenter Real-World Retrospective Study.

作者信息

Baser Mehmet Nuri, Demir Bilgin, Serin Ozel Gamze, Dogu Gamze Gokoz, Karakaya Serdar, Ugar Mucahit, Ak Naziye, Ozveren Ahmet, Camanlı Ufuk, Unal Olcun Umit, Turan Merve, Oktay Esin

机构信息

Department of Medical Oncology, Faculty of Medicine, Adnan Menderes University, Aydin 09010, Turkey.

Department of Medical Oncology, Faculty of Medicine, Pamukkale University, Denizli 20160, Turkey.

出版信息

Medicina (Kaunas). 2025 Jul 7;61(7):1230. doi: 10.3390/medicina61071230.

Abstract

Small-cell lung cancer (SCLC) is an exceedingly aggressive neoplasm distinguished by an unfavorable prognosis. Recent studies have confirmed chemo-immunotherapy as the conventional first treatment for extensive-stage small-cell lung cancer (ES-SCLC), but the impact of treatment duration remains unclear. The goal of this study was to find out how the length of treatment affected progression-free survival (PFS) and overall survival (OS) in patients with ES-SCLC who were receiving first-line atezolizumab plus chemotherapy. This retrospective multicenter study comprised 82 patients from six oncology centers in Turkey between 2017 and 2024. Patients were categorized into two categories according to the quantity of chemotherapy cycles they had undergone: standard treatment (≤4 cycles) and extended treatment (≥5 cycles). For the purpose of analyzing survival outcomes and related clinical determinants, as well as the demographic structures and features of the patients, both univariate and multivariate Cox regression models were utilized. The median number of atezolizumab cycles was 8 (1-63). OS was 29.46 months after 15.8 months of follow-up, while PFS was 10.63 months. When comparing the two groups, we found no statistically significant differences in either PFS ( = 0.952) or OS ( = 0.374). Significant associations with OS were seen in the standard therapy group for both ECOG PS 1 ( = 0.028). Thoracic radiation considerably decreased progression risk (HR = 0.41, = 0.031) in the extended group. While prolonging chemo-immunotherapy beyond four cycles did not significantly improve survival, the selected patient subgroups may benefit from personalized approaches. Thoracic radiotherapy emerged as a key modifier of outcome.

摘要

小细胞肺癌(SCLC)是一种极具侵袭性的肿瘤,预后不良。最近的研究已证实化疗免疫疗法是广泛期小细胞肺癌(ES-SCLC)的传统一线治疗方法,但治疗持续时间的影响仍不明确。本研究的目的是了解治疗时长如何影响接受一线阿替利珠单抗联合化疗的ES-SCLC患者的无进展生存期(PFS)和总生存期(OS)。这项回顾性多中心研究纳入了2017年至2024年间来自土耳其六个肿瘤中心的82例患者。根据患者接受化疗周期的数量将其分为两类:标准治疗(≤4个周期)和延长治疗(≥5个周期)。为了分析生存结果和相关临床决定因素以及患者的人口统计学结构和特征,使用了单变量和多变量Cox回归模型。阿替利珠单抗周期的中位数为8(1 - 63)。随访15.8个月后,OS为29.46个月,而PFS为10.63个月。比较两组时,我们发现PFS( = 0.952)或OS( = 0.374)均无统计学显著差异。在标准治疗组中,ECOG PS 1与OS均存在显著关联( = 0.028)。胸部放疗在延长治疗组中显著降低了进展风险(HR = 0.41, = 0.031)。虽然将化疗免疫疗法延长至四个周期以上并未显著改善生存率,但选定的患者亚组可能从个性化方法中受益。胸部放疗成为结果的关键调节因素。

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