Suppr超能文献

评估阿替利珠单抗对日本接受化疗的非小细胞肺癌患者发热性中性粒细胞减少症发生情况的影响:一项真实世界的上市后数据库研究。

Evaluating the impact of atezolizumab on febrile neutropenia occurrence in patients with NSCLC undergoing chemotherapy in Japan: a real-world post-marketing database study.

作者信息

Nakane Sayuri, Yuri Akinori, Miyano Yuki, Yamada Kana, Nakatsuji Erika, Takei Nobuki, Igarashi Yasuhiro, Harada Ryousuke

机构信息

Safety Science 2 Department, Drug Safety Division, Chugai Pharmaceutical Co., Ltd., 1-1 Nihonbashi-Muromachi 2-Chome, Chuo-Ku, Tokyo, 103-8324, Japan.

Safety Science 1 Department, Drug Safety Division, Chugai Pharmaceutical Co., Ltd., Chuo-Ku, Japan.

出版信息

Int J Clin Oncol. 2025 Feb;30(2):298-308. doi: 10.1007/s10147-024-02669-y. Epub 2024 Dec 16.

Abstract

BACKGROUND

Febrile neutropenia (FN) is a recognised adverse event associated with chemotherapy. This study investigates the impact of atezolizumab, an immune checkpoint inhibitor, on the incidence of FN in patients with non-small cell lung cancer receiving concurrent chemotherapy in Japan.

METHODS

This post-marketing database study was conducted using data from patients with non-small cell lung cancer provided by Medical Data Vision Co., Ltd. covering April 2008 to present. The primary outcome measured was FN incidence, and its causal association with atezolizumab use was examined by comparing the atezolizumab plus bevacizumab plus carboplatin plus paclitaxel [ABCP])-containing regimen to the BCP control group. The data period was from 1 September, 2015, to 31 December, 2021, including approval date of this drug, 21 December, 2018.

RESULTS

The database identified 301 subjects for the ABCP regimen (exposure) group, 44 for the BCP regimen (cohort design control) group during the same period, and 207 for BCP regimen (historical cohort design control) group before the approval of atezolizumab. For historical cohort design, the incidence and adjusted incidence ratios of febrile neutropenia in the exposure group to the control group were 6.13 (95% CI 2.78-13.49) and 8.19 (95% CI 3.79-25.33), respectively. Sensitivity analysis showed FN occurred in 17% (52/301) of the exposure group, 4.5% (2/44) of the cohort design control group, and 3% (7/207) of the historical cohort design control group.

CONCLUSIONS

The incidence of FN was higher in the exposure group. Considering the study results, special caution is needed for FN occurrence in patients receiving atezolizumab.

摘要

背景

发热性中性粒细胞减少症(FN)是一种与化疗相关的公认不良事件。本研究调查了免疫检查点抑制剂阿替利珠单抗对日本接受同步化疗的非小细胞肺癌患者FN发生率的影响。

方法

本上市后数据库研究使用了Medical Data Vision Co., Ltd.提供的2008年4月至今的非小细胞肺癌患者数据。测量的主要结局是FN发生率,并通过比较含阿替利珠单抗加贝伐珠单抗加卡铂加紫杉醇[ABCP])方案与BCP对照组,研究其与阿替利珠单抗使用的因果关系。数据期为2015年9月1日至2021年12月31日,包括该药物的批准日期2018年12月21日。

结果

数据库确定ABCP方案(暴露)组有301名受试者,同期BCP方案(队列设计对照)组有44名受试者,阿替利珠单抗批准前BCP方案(历史队列设计对照)组有207名受试者。对于历史队列设计,暴露组发热性中性粒细胞减少症的发生率和调整后的发生率分别为6.13(95%CI 2.78 - 13.49)和8.19(95%CI 3.79 - 25.33)。敏感性分析显示,暴露组17%(52/301)发生FN,队列设计对照组4.5%(2/44)发生FN,历史队列设计对照组3%(7/207)发生FN。

结论

暴露组FN发生率较高。考虑到研究结果,接受阿替利珠单抗治疗的患者发生FN时需要特别谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b89/11785710/884341489fd8/10147_2024_2669_Fig1_HTML.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验