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化疗免疫治疗后氨柔比星治疗小细胞肺癌患者的疗效与安全性

Efficacy and safety of amrubicin therapy after chemoimmunotherapy in small cell lung cancer patients.

作者信息

Kushiro Kohei, Watanabe Satoshi, Goto Yuka, Fujisaki Toshiya, Yanagimura Naohiro, Ohtsubo Aya, Shoji Satoshi, Nozaki Koichiro, Tanaka Tomohiro, Saida Yu, Sato Yusuke, Ota Takeshi, Koshio Jun, Hayashi Yoshiki, Miyabayashi Takao, Matsumoto Naoya, Ichikawa Kosuke, Koyama Kenichi, Kikuchi Toshiaki

机构信息

Department of Respiratory Medicine and Infectious Diseases, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.

Niigata Prefectural Sakamachi Hospital, Niigata, Japan.

出版信息

Transl Lung Cancer Res. 2022 Sep;11(9):1858-1865. doi: 10.21037/tlcr-22-225.

Abstract

BACKGROUND

Although the addition of immune checkpoint inhibitors (ICIs) to platinum-doublet chemotherapy has improved the efficacy of first-line therapy in extensive-disease small cell lung cancer (SCLC) patients, the best treatment option for patients with recurrent SCLC has not yet been determined. We conducted a retrospective study to evaluate the efficacy and safety of amrubicin (AMR) therapy after treatment with ICIs.

METHODS

We retrospectively assessed patients with recurrent SCLC who received AMR after chemoimmunotherapy at the Niigata Lung Cancer Treatment Group from August 2019 to February 2021.

RESULTS

This analysis included 30 patients. The median progression-free survival (PFS) and overall survival (OS) were 3.8 (95% CI: 2.7-4.2) and 10 (95% CI: 7.4-14.8) months, respectively. The median PFS and OS did not significantly differ between the sensitive and refractory groups [PFS; 3.1 (95% CI: 1.1-4.0) 4.2 (95% CI: 2.3-4.8) months, P=0.1142, OS; 10.0 (95% CI: 5.2-14.8) 10.4 (95% CI: 3.8-NE) months, P=0.5525]. The most common adverse event was grade ≥3 neutropenia, which occurred in 22 of 30 patients (73%), and 2 patients (7%) discontinued AMR due to adverse events.

CONCLUSIONS

AMR after chemoimmunotherapy shows good clinical efficacy and safety in patients with recurrent SCLC.

摘要

背景

尽管在铂类双联化疗中添加免疫检查点抑制剂(ICI)提高了广泛期小细胞肺癌(SCLC)患者一线治疗的疗效,但复发性SCLC患者的最佳治疗方案尚未确定。我们进行了一项回顾性研究,以评估ICI治疗后氨柔比星(AMR)治疗的疗效和安全性。

方法

我们回顾性评估了2019年8月至2021年2月在新潟肺癌治疗组接受化疗免疫治疗后接受AMR的复发性SCLC患者。

结果

该分析纳入了30例患者。中位无进展生存期(PFS)和总生存期(OS)分别为3.8个月(95%CI:2.7 - 4.2)和10个月(95%CI:7.4 - 14.8)。敏感组和难治组之间的中位PFS和OS无显著差异[PFS;3.1个月(95%CI:1.1 - 4.0)对4.2个月(95%CI:2.3 - 4.8),P = 0.1142,OS;10.0个月(95%CI:5.2 - 14.8)对10.4个月(95%CI:3.8 - NE),P = 0.5525]。最常见的不良事件是≥3级中性粒细胞减少,30例患者中有22例(73%)发生,2例(7%)患者因不良事件停用AMR。

结论

化疗免疫治疗后使用AMR对复发性SCLC患者显示出良好的临床疗效和安全性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65fc/9554694/b02dae6b7d88/tlcr-11-09-1858-f1.jpg

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