Suppr超能文献

质子泵抑制剂和蛋白激酶抑制剂暴露与肺癌患者生存的有害关联:一项全国性队列研究。

Deleterious association between proton pump inhibitor and protein kinase inhibitor exposure and survival for patients with lung cancer: A nationwide cohort study.

机构信息

Medical and Clinical Pharmacology Department, Faculty of Medicine, Pharmacovigilance, Pharmacoepidemiology and Drug Information Center, CIC INSERM 1436, Faculty of Medicine, University Hospital Center, 31000, Toulouse, France.

EPI-PHARE, French National Agency for Medicines and Health Products Safety, French National Health Insurance, Saint-Denis, France.

出版信息

Cancer Treat Res Commun. 2024;39:100801. doi: 10.1016/j.ctarc.2024.100801. Epub 2024 Feb 29.

Abstract

INTRODUCTION

Previous studies have identified an interaction between protein kinase inhibitors (PKIs) and proton pump inhibitors (PPIs) in patients with lung cancer. This type of interaction may reduce the efficacy of PKIs. However, the effect of PKI-PPI interaction on patient mortality remains controversial. This study set out to determine the impact of PKI-PPI interaction on overall survival for lung cancer patients.

MATERIALS AND METHODS

This study was conducted using data from the French National Health Care Database from January 1, 2011 to December 31, 2021. We identified patients with: (i) an age equal to or greater than 18 years; (ii) lung cancer; and (iii) at least one reimbursement for one of the following drugs: erlotinib, gefitinib, afatinib and osimertinib. Patients were followed-up between the first date of PKI reimbursement and either December 31, 2021 or if they died, the date on which death occurred. The cumulative exposure to PPI duration during PKI treatment was calculated as the ratio between the number of concomitant exposure days to PKI and PPI and the number of exposure days to PKI. A survival analysis using a Cox proportional hazards model was then performed to assess the risk of death following exposure to a PKI-PPI interaction.

RESULTS

34,048 patients received at least one reimbursement for PKIs of interest in our study: 26,133 (76.8 %) were exposed to erlotinib; 3,142 (9.2 %) to gefitinib; 1,417 (4.2 %) to afatinib; and 3,356 (9.9 %) to osimertinib. Patients with concomitant exposure to PKI-PPI interaction during 20 % or more of the PKI treatment period demonstrated an increased risk of death (HR, 1.60 [95 % CI, 1.57-1.64]) compared to other patients. When this cut-off varied from 10 % to 80 %, the estimated HR ranged from 1.46 [95 % CI, 1.43-1.50] to 2.19 [95 % CI, 2.12-2.25].

DISCUSSION/CONCLUSION: In our study, an elevated risk of death was observed in patients exposed to PKI-PPI interaction. Finally, we were able to identify a dose-dependent effect for this interaction. This deleterious effect of osimertinib and PPI was revealed for the first time in real life conditions.

摘要

简介

先前的研究已经确定了肺癌患者中蛋白激酶抑制剂(PKIs)和质子泵抑制剂(PPIs)之间的相互作用。这种相互作用可能会降低 PKIs 的疗效。然而,PKI-PPI 相互作用对患者死亡率的影响仍存在争议。本研究旨在确定 PKI-PPI 相互作用对肺癌患者总生存期的影响。

材料和方法

本研究使用了 2011 年 1 月 1 日至 2021 年 12 月 31 日期间法国国家医疗保健数据库的数据。我们确定了以下患者:(i)年龄等于或大于 18 岁;(ii)患有肺癌;(iii)至少有一次以下药物之一的报销:厄洛替尼、吉非替尼、阿法替尼和奥希替尼。患者在 PKI 报销的第一个日期至 2021 年 12 月 31 日之间或死亡日期(死亡发生之日)之间进行随访。在 PKI 治疗期间,通过将同时使用 PKI 和 PPI 的天数与 PKI 的使用天数进行比较来计算 PPI 持续时间的累积暴露比。然后使用 Cox 比例风险模型进行生存分析,以评估暴露于 PKI-PPI 相互作用后的死亡风险。

结果

在我们的研究中,有 34048 名患者至少接受了一次我们感兴趣的 PKI 报销:26133 名(76.8%)患者接受了厄洛替尼治疗;3142 名(9.2%)接受了吉非替尼治疗;1417 名(4.2%)接受了阿法替尼治疗;3356 名(9.9%)接受了奥希替尼治疗。与其他患者相比,在 PKI 治疗期间有 20%或更多时间同时暴露于 PKI-PPI 相互作用的患者死亡风险增加(HR,1.60[95%CI,1.57-1.64])。当这个截止值从 10%变化到 80%时,估计的 HR 范围从 1.46[95%CI,1.43-1.50]到 2.19[95%CI,2.12-2.25]。

讨论/结论:在我们的研究中,暴露于 PKI-PPI 相互作用的患者死亡风险增加。最后,我们能够确定这种相互作用存在剂量依赖性效应。在现实生活条件下,奥希替尼和 PPI 的这种有害作用首次被揭示。

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