First-line atezolizumab/durvalumab plus platinum–etoposide combined with radiotherapy in extensive-stage small-cell lung cancer

阿替唑单抗 医学 杜瓦卢马布 放射治疗 肿瘤科 肺炎 内科学 免疫疗法 依托泊苷 化学免疫疗法 外科 化疗 癌症 彭布罗利珠单抗
作者
Lijuan Li,Dan Yang,Yanmei Min,Anyan Liao,Jing Zhao,Leilei Jiang,Xin Dong,Wei Deng,Huiming Yu,Rong Yu,Jun Zhao,Anhui Shi
出处
期刊:BMC Cancer [BioMed Central]
卷期号:23 (1) 被引量:14
标识
DOI:10.1186/s12885-023-10784-8
摘要

Immunotherapy has made significant advances in the treatment of extensive-stage small-cell lung cancer (ES-SCLC), but data in combination with radiotherapy are scarce. This study aims to assess the safety and efficacy of chemoimmunotherapy combined with thoracic radiotherapy in patients with ES-SCLC.This single-center retrospective study analyzed patients with ES-SCLC who received standard platinum-etoposide chemotherapy combined with atezolizumab or durvalumab immunotherapy as induction treatment, followed by consolidative thoracic radiotherapy (CTRT) before disease progression in the first-line setting. Adverse events during radiotherapy with or without maintenance immunotherapy and survival outcomes were assessed.Between December 2019 and November 2021, 36 patients with ES-SCLC were identified to have received such treatment modality at one hospital. The number of metastatic sites at diagnosis was 1-4. The biological effective dose of CTRT ranged from 52 to 113 Gy. Only two patients (6%) developed grade 3 toxic effect of thrombocytopenia, but none experienced grade 4 or 5 toxicity. Four patients developed immune-related pneumonitis during the induction treatment period but successfully completed later CTRT. The rate of radiation-related pneumonitis was 8% with grades 1-2 and well tolerated. The median progression-free survival (PFS) was 12.8 months, but the median overall survival (OS) was not determined. The estimated 1-year OS was 80.2% and 1-year PFS was 53.4%.Immunotherapy combined with CTRT for ES-SCLC is safe and has ample survival benefit.
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