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不同间变性淋巴瘤激酶酪氨酸激酶抑制剂方案治疗后肺炎的发生率:一项更新的系统评价和荟萃分析。

Incidence of pneumonitis following the use of different anaplastic lymphoma kinase tyrosine kinase inhibitor regimens: An updated systematic review and meta-analysis.

机构信息

Department of Oncology, Weifang Medical University, Weifang, Shandong, People's Republic of China.

Department of Radiation Oncology, Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Sciences, Jinan, Shandong, People's Republic of China.

出版信息

Cancer Med. 2023 Jul;12(13):13873-13884. doi: 10.1002/cam4.5913. Epub 2023 Apr 5.

Abstract

OBJECTIVES

Anaplastic lymphoma kinase tyrosine kinase inhibitors (ALK TKIs) have shown remarkable clinical activity in patients with non-small-cell lung cancer (NSCLC). However, pneumonitis is a serious side effect of ALK TKIs in NSCLC patients. In this meta-analysis, we aimed to determine the incidence of ALK-TKI-associated pneumonitis.

MATERIALS AND METHODS

We searched electronic databases to identify relevant studies published until August 2022. The incidence of pneumonitis was calculated using a fixed-effects model when no substantial heterogeneity was observed. Otherwise, a random-effects model was used. Subgroup analyses of different treatment groups were performed. Statistical analyses were conducted using STATA 17.0.

RESULTS

Twenty-six clinical trials involving 4752 patients were eligible for analysis. All-grade pneumonitis incidence was 2.92% (95% confidence interval [CI]: 1.79%-4.27%), high-grade (Grade 3-4) pneumonitis incidence was 1.42% (95% CI: 0.84%-2.12%) and Grade 5 pneumonitis incidence was 0.09% (95% CI: 0.00%-0.28%). The subgroup analysis showed that brigatinib was associated with the highest incidence of both all-grade and high-grade pneumonitis (7.09% and 3.06%, respectively). ALK TKI treatment after chemotherapy was associated with a higher incidence of all-grade and high-grade pneumonitis than first-line ALK TKI treatment (7.73% vs. 2.26% and 3.64% vs. 1.26%, respectively). Cohorts from Japanese trials had a higher incidence of all-grade and high-grade pneumonitis.

CONCLUSION

Our study provides precise data on the incidence of pneumonitis in patients receiving treatment with ALK TKIs. Overall, ALK TKIs have tolerable pulmonary toxicity. Early pneumonitis identification and treatment are required to prevent further deterioration in patients receiving treatment with brigatinib and in those who received prior chemotherapy, particularly in the Japanese population.

摘要

目的

间变性淋巴瘤激酶酪氨酸激酶抑制剂(ALK-TKIs)在非小细胞肺癌(NSCLC)患者中表现出显著的临床活性。然而,间变性淋巴瘤激酶酪氨酸激酶抑制剂相关的肺炎是 NSCLC 患者的一种严重副作用。在这项荟萃分析中,我们旨在确定 ALK-TKI 相关肺炎的发生率。

材料和方法

我们检索了电子数据库,以确定截至 2022 年 8 月发表的相关研究。当没有观察到实质性异质性时,使用固定效应模型计算肺炎的发生率。否则,使用随机效应模型。对不同治疗组进行亚组分析。使用 STATA 17.0 进行统计分析。

结果

共有 26 项临床试验纳入了 4752 名患者进行分析。所有级别肺炎的发生率为 2.92%(95%置信区间 [CI]:1.79%-4.27%),高级别(3-4 级)肺炎的发生率为 1.42%(95% CI:0.84%-2.12%),5 级肺炎的发生率为 0.09%(95% CI:0.00%-0.28%)。亚组分析显示,布加替尼与所有级别和高级别肺炎的发生率最高(分别为 7.09%和 3.06%)。与一线 ALK-TKI 治疗相比,化疗后 ALK-TKI 治疗与所有级别和高级别肺炎的发生率更高(分别为 7.73%比 2.26%和 3.64%比 1.26%)。来自日本试验的队列具有更高的所有级别和高级别肺炎发生率。

结论

我们的研究提供了接受 ALK-TKI 治疗的患者发生肺炎的发生率的确切数据。总体而言,ALK-TKI 具有可耐受的肺毒性。需要早期识别和治疗肺炎,以防止接受布加替尼和接受过化疗的患者病情进一步恶化,特别是在日本人群中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7df7/10358266/9a7a5067ba18/CAM4-12-13873-g004.jpg

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