Suppr超能文献

伊立替康单药治疗作为小细胞肺癌三线或后线治疗。

Irinotecan monotherapy as third- or further-line treatment for patients with small cell lung cancer.

机构信息

First Department of Internal Medicine, Toyama University Hospital, Toyama, Japan.

Department of Medical Oncology, Toyama University Hospital, Toyama, Japan.

出版信息

Tumori. 2021 Dec;107(6):536-541. doi: 10.1177/0300891620974762. Epub 2020 Nov 25.

Abstract

BACKGROUND

Small cell lung cancer (SCLC) is a very aggressive cancer and recurrence is inevitable. Treatment of recurrent disease is important for improving the prognosis of patients with SCLC.

METHODS

We conducted a retrospective observational study to investigate the efficacy and safety of irinotecan monotherapy as third- or further-line treatment in patients with SCLC.

RESULTS

Data of 15 patients who had received irinotecan monotherapy as third- or further-line treatment between 2004 and 2019 were analyzed. The median progression-free survival duration (95% confidence interval) from the initiation of treatment with irinotecan was 2.7 (1.4-3.8) months, and the median overall survival duration (95% confidence interval) from the initiation of irinotecan treatment was 10.0 (3.9-12.9) months. Partial response, stable disease or non-complete response/non-progressive disease, and progressive disease were observed in 1, 6, and 8 patients, respectively. Adverse events ⩾ grade 3 in severity were observed in 2/2 (100%) patients who were homozygous for mutation, 2/3 (66.7%) patients who were heterozygous for mutation, 4/6 (66.7%) patients who had wild-type , and 2/4 (50.0%) patients in whom the mutation status was unknown.

CONCLUSION

Our results suggest that irinotecan monotherapy can be a useful alternative treatment option in the third-line setting for patients with SCLC.

摘要

背景

小细胞肺癌(SCLC)是一种侵袭性很强的癌症,复发是不可避免的。治疗复发性疾病对于改善 SCLC 患者的预后非常重要。

方法

我们进行了一项回顾性观察性研究,以调查伊立替康单药治疗作为三线或更后线治疗 SCLC 患者的疗效和安全性。

结果

分析了 2004 年至 2019 年间接受伊立替康三线或更后线单药治疗的 15 例患者的数据。从开始伊立替康治疗到无进展生存期的中位数(95%置信区间)为 2.7(1.4-3.8)个月,从开始伊立替康治疗到总生存期的中位数(95%置信区间)为 10.0(3.9-12.9)个月。1 例患者部分缓解,6 例患者稳定疾病或非完全缓解/非进展性疾病,8 例患者进展疾病。2 例纯合突变患者(100%)、3 例杂合突变患者中的 2 例(66.7%)、6 例野生型患者中的 4 例(66.7%)和 4 例未知突变状态的患者中的 2 例(50.0%)出现 ⩾3 级严重不良事件。

结论

我们的结果表明,伊立替康单药治疗可能是三线治疗 SCLC 患者的一种有用的替代治疗选择。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验