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质子泵抑制剂对非小细胞肺癌患者中表皮生长因子受体酪氨酸激酶抑制剂相关间质性肺疾病的影响。

PPIs effect in EGFR-TKI-associated interstitial lung diseases in patients with non-small cell lung cancer.

作者信息

Wang Haitao, Chen Keyu, Ma Sinan, Huang Weijia, Xie Jiao, Wang Na, Li Youjia, Yang Qianting, Yang Xin, Wang Yan

机构信息

Department of Pharmacy, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China.

出版信息

BMC Cancer. 2025 Feb 14;25(1):263. doi: 10.1186/s12885-025-13673-4.

Abstract

BACKGROUND

Previous studies suggest a potential link between interstitial lung diseases (ILD) and EGFR-TKI use, with proton pump inhibitors (PPIs) possibly affecting EGFR-TKI-associated ILD differently. Our objective is to use the US Food and Drug Administration Adverse Event Reporting System (FAERS) database to explore the potential link between ILD and the combination of PPIs and EGFR-TKI.

METHODS

A retrospective examination of adverse event reports in the FAERS database spanning from the initial quarter of 2016 and the fourth quarter of 2023 was conducted. Disproportionality analysis, generalized linear models, and adjusted multivariable logistic regression were employed to assess the occurrence of EGFR-TKI-associated ILD in non-small cell lung cancer (NSCLC) patients receiving PPIs compared to those not receiving PPIs.

RESULTS

The reporting odds ratio (ROR) for PPIs combined with EGFR-TKIs demonstrated statistical significance (ROR 1.84, 95% CI 1.54-2.19). Significant increases were noted in both additive and multiplicative models (p < 0.001), as well as in the adjusted odds ratios derived from multivariate analysis (1.77, 95% CI 1.42-2.19, p < 0.001). Stratified analysis reveals that the combination of lansoprazole or esomeprazole and EGFR-TKI was linked to an elevated risk of ILD, with a ROR of 2.37 (95% CI 1.84-3.04) and 2.90 (95% CI 2.11-3.98), respectively, surpassing the risk associated with either medication used independently. Similarly, the ROR for osimertinib or gefitinib combined with PPIs stands at 2.20 (95% CI 1.83-2.66) and 2.33 (1.35-4.02), respectively, exceeding the risk when either drug is used alone.

CONCLUSIONS

Our study uncovered a heightened risk of ILD in NSCLC patients receiving certain EGFR-TKI in conjunction with specific PPIs, as opposed to EGFR-TKI monotherapy. Subsequent analysis indicates that different PPIs may elicit divergent effects on EGFR-TKI-associated ILD, with different EGFR-TKIs exhibiting distinct responses to combinations with different PPIs. Therefore, NSCLC patients undergoing such treatments should be meticulously monitored for ILD.

摘要

背景

先前的研究表明间质性肺疾病(ILD)与表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKI)的使用之间可能存在联系,质子泵抑制剂(PPI)可能对EGFR-TKI相关的ILD产生不同影响。我们的目标是利用美国食品药品监督管理局不良事件报告系统(FAERS)数据库,探索ILD与PPI和EGFR-TKI联合使用之间的潜在联系。

方法

对FAERS数据库中2016年第一季度至2023年第四季度的不良事件报告进行回顾性审查。采用不成比例分析、广义线性模型和调整后的多变量逻辑回归,评估接受PPI的非小细胞肺癌(NSCLC)患者与未接受PPI的患者相比,EGFR-TKI相关ILD的发生情况。

结果

PPI与EGFR-TKI联合使用的报告比值比(ROR)具有统计学意义(ROR 1.84,95%置信区间1.54-2.19)。在相加模型和相乘模型中均观察到显著增加(p<0.001),多变量分析得出的调整后比值比也显著增加(1.77,95%置信区间1.42-2.19,p<0.001)。分层分析显示,兰索拉唑或埃索美拉唑与EGFR-TKI联合使用与ILD风险升高相关,ROR分别为2.37(95%置信区间1.84-3.04)和2.90(95%置信区间2.11-3.98),超过单独使用任何一种药物的风险。同样,奥希替尼或吉非替尼与PPI联合使用的ROR分别为2.20(95%置信区间1.83-2.66)和2.33(1.35-4.02),超过单独使用任何一种药物的风险。

结论

我们的研究发现,与EGFR-TKI单药治疗相比,接受某些EGFR-TKI与特定PPI联合治疗的NSCLC患者发生ILD的风险更高。后续分析表明,不同的PPI可能对EGFR-TKI相关的ILD产生不同影响,不同的EGFR-TKI与不同的PPI联合使用时表现出不同的反应。因此,接受此类治疗的NSCLC患者应密切监测ILD。

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