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巩固性胸部放疗改善化疗免疫治疗时代广泛期小细胞肺癌患者的预后:一项多中心回顾性分析

Consolidative thoracic radiotherapy improves the prognosis of extensive stage small-cell lung cancer patients in the chemoimmunotherapy era: a multicenter retrospective analysis.

作者信息

Yao Nan, Li Shuai, Hu Lingling, Pei Yixian, Qin Zhaohui, Li Na, Tong Shaodong, Zhang Nan, Yao Yuanhu

机构信息

Department of Radiation Oncology, The Affiliated Wuxi People's Hospital of Nanjing Medical University, Wuxi, Jiangsu, China.

Wuxi Medical Center, Nanjing Medical University, Wuxi, Jiangsu, China.

出版信息

Ann Med. 2025 Dec;57(1):2542434. doi: 10.1080/07853890.2025.2542434. Epub 2025 Aug 4.

DOI:10.1080/07853890.2025.2542434
PMID:40755353
Abstract

BACKGROUND

For extensive-stage small cell lung cancer (ES-SCLC) with intrathoracic residuals after chemotherapy, the landmark CREST trial demonstrated the benefit of consolidative thoracic radiotherapy (cTRT). Yet the efficacy and safety of cTRT after chemoimmunotherapy for ES-SCLC remain largely unknown. This study aimed to assess the role of cTRT following chemoimmunotherapy in patients with ES-SCLC.

METHODS

A retrospective analysis of ES-SCLC patients without disease progression after first-line chemoimmunotherapy was conducted between March 2019 and November 2021. Based on whether cTRT or not, patients were allocated to cTRT group or non-cTRT group. We evaluated efficacy by using the median overall survival (mOS) and progression-free survival (mPFS) times, and safety by measuring the incidence of adverse events.

RESULTS

During this study, 72 patients with ES-SCLC were enrolled, with a median follow-up of 34.66 months. Twenty-nine patients received cTRT and 43 patients did not receive cTRT. Among the cTRT group and the non-cTRT group, the mPFS was 11.50 and 8.02 months, respectively, with a HR of 0.60 (95% CI 0.36-0.99,  = 0.043). The mOS in the cTRT group was also significantly longer than that in the non-cTRT group (28.68 months vs. 16.30 months, HR = 0.56, 95% CI 0.32-0.96,  = 0.033). Based on multivariate analysis, cTRT and cycles of immunotherapy ≥ 6 were independent factors affecting survival. There were no treatment-related deaths and most adverse events were grade 1-2.

CONCLUSIONS

This study suggests that the addition of cTRT to first-line chemo-immunotherapy significantly improves survival in ES-SCLC with well-tolerated toxicity.

摘要

背景

对于化疗后有胸腔内残留的广泛期小细胞肺癌(ES-SCLC),具有里程碑意义的CREST试验证明了巩固性胸部放疗(cTRT)的益处。然而,化疗免疫治疗后cTRT用于ES-SCLC的疗效和安全性仍 largely未知。本研究旨在评估cTRT在ES-SCLC患者化疗免疫治疗后的作用。

方法

对2019年3月至2021年11月期间一线化疗免疫治疗后无疾病进展的ES-SCLC患者进行回顾性分析。根据是否接受cTRT,将患者分为cTRT组和非cTRT组。我们通过使用中位总生存期(mOS)和无进展生存期(mPFS)来评估疗效,并通过测量不良事件的发生率来评估安全性。

结果

在本研究期间,纳入了72例ES-SCLC患者,中位随访时间为34.66个月。29例患者接受了cTRT,43例患者未接受cTRT。在cTRT组和非cTRT组中,mPFS分别为11.50个月和8.02个月,HR为0.60(95%CI 0.36-0.99,P = 0.043)。cTRT组的mOS也显著长于非cTRT组(28.68个月对16.30个月,HR = 0.56,95%CI 0.32-0.96,P = 0.033)。基于多变量分析,cTRT和免疫治疗周期≥6是影响生存的独立因素。没有与治疗相关的死亡,大多数不良事件为1-2级。

结论

本研究表明,在一线化疗免疫治疗中添加cTRT可显著提高ES-SCLC的生存率,且毒性耐受性良好。

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Efficacy and safety of thoracic radiotherapy in extensive-stage small-cell lung cancer patients receiving first-line immunotherapy plus chemotherapy: a propensity score matched multicentre retrospective analysis.一线免疫治疗联合化疗的广泛期小细胞肺癌患者接受胸部放疗的疗效和安全性:一项倾向评分匹配的多中心回顾性分析。
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