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广泛期小细胞肺癌一线化疗免疫治疗后胸部放疗的真实世界疗效与安全性

Real-World Efficacy and Safety of Thoracic Radiotherapy after First-Line Chemo-Immunotherapy in Extensive-Stage Small-Cell Lung Cancer.

作者信息

Xie Zhaoliang, Liu Jingru, Wu Min, Wang Xiaohan, Lu Yuhan, Han Chunyan, Cong Lei, Li Jisheng, Meng Xue

机构信息

Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Science, Jinan 250117, China.

Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong University Cancer Center, Jinan 250117, China.

出版信息

J Clin Med. 2023 Jun 2;12(11):3828. doi: 10.3390/jcm12113828.

DOI:10.3390/jcm12113828
PMID:37298023
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10253710/
Abstract

(1) Background: At present, the efficacy and safety of thoracic radiotherapy (TRT) after chemo-immunotherapy (CT-IT) in patients with extensive-stage small-cell lung cancer (ES-SCLC) still remain unclear. The purpose of this study was to evaluate the role of TRT after CT-IT in patients with ES-SCLC. (2) Methods: From January 2020 to October 2021, patients with ES-SCLC treated with first-line anti-PD-L1 antibody plus platinum-etoposide chemotherapy were enrolled retrospectively. The survival data and adverse events data of patients treated with or without TRT after CT-IT were collected for analysis. (3) Results: A total of 118 patients with ES-SCLC treated with first-line CT-IT were retrospectively enrolled, with 45 patients with TRT and 73 patients without TRT after CT-IT. The median PFS and OS in the CT-IT + TRT group and CT-IT only group were 8.0 months versus 5.9 months (HR = 0.64, = 0.025) and 22.7 months versus 14.7 months (HR = 0.52, = 0.015), respectively. The median PFS and OS in all 118 patients treated with first-line CT-IT were 7.2 and 19.8 months with an ORR of 72.0%. In multivariate analyses, liver metastasis and response to CT-IT were shown to be independent prognostic factors of PFS ( < 0.05), while liver metastasis and bone metastasis were independent predictive factors of OS ( < 0.05). Although TRT was significantly associated with better PFS and OS in univariate analysis, the association of TRT and OS failed to reach statistical significance (HR = 0.564, = 0.052) in multivariate analysis. There was no significant difference in adverse events (AEs) between two treatment groups ( = 0.58). (4) Conclusions: ES-SCLC patients treated with TRT after first-line CT-IT had prolonged PFS and OS with an acceptable safety profile. Further prospective randomized studies are necessary to explore the efficacy and safety of this treatment modality for ES-SCLC in future.

摘要

(1) 背景:目前,广泛期小细胞肺癌(ES-SCLC)患者在化疗免疫治疗(CT-IT)后进行胸部放疗(TRT)的疗效和安全性仍不明确。本研究旨在评估CT-IT后TRT在ES-SCLC患者中的作用。(2) 方法:回顾性纳入2020年1月至2021年10月接受一线抗PD-L1抗体联合铂类-依托泊苷化疗的ES-SCLC患者。收集CT-IT后接受或未接受TRT治疗患者的生存数据和不良事件数据进行分析。(3) 结果:共回顾性纳入118例接受一线CT-IT治疗的ES-SCLC患者,其中45例在CT-IT后接受TRT,73例未接受TRT。CT-IT + TRT组和单纯CT-IT组的中位无进展生存期(PFS)分别为8.0个月和5.9个月(风险比[HR]=0.64,P=0.025),中位总生存期(OS)分别为22.7个月和14.7个月(HR=0.52,P=0.015)。118例接受一线CT-IT治疗的患者的中位PFS和OS分别为7.2个月和19.8个月,客观缓解率(ORR)为72.0%。多因素分析显示,肝转移和对CT-IT的反应是PFS的独立预后因素(P<0.05),而肝转移和骨转移是OS的独立预测因素(P<0.05)。虽然在单因素分析中TRT与更好的PFS和OS显著相关,但在多因素分析中TRT与OS的关联未达到统计学意义(HR=0.564,P=0.052)。两个治疗组之间的不良事件(AE)无显著差异(P=0.58)。(4) 结论:一线CT-IT后接受TRT治疗的ES-SCLC患者PFS和OS延长,安全性可接受。未来有必要进行进一步的前瞻性随机研究,以探索这种治疗方式对ES-SCLC的疗效和安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9568/10253710/4db97c8b97c6/jcm-12-03828-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9568/10253710/c5d86e5dad36/jcm-12-03828-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9568/10253710/9edb94433ed3/jcm-12-03828-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9568/10253710/3725d62fe088/jcm-12-03828-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9568/10253710/4db97c8b97c6/jcm-12-03828-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9568/10253710/c5d86e5dad36/jcm-12-03828-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9568/10253710/9edb94433ed3/jcm-12-03828-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9568/10253710/3725d62fe088/jcm-12-03828-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9568/10253710/4db97c8b97c6/jcm-12-03828-g004.jpg

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