质子泵抑制剂和蛋白激酶抑制剂暴露与肺癌患者生存之间的畸变关系:一项全国性队列研究

Constance Bordet , Mahmoud Zureik , Yoann Zelmat , Margaux Lafaurie , Maryse Lapeyre-Mestre , Agnès Sommet , Julien Mazieres , Fabien Despas
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引用次数: 0

摘要

导言先前的研究发现,在肺癌患者中,蛋白激酶抑制剂(PKIs)与质子泵抑制剂(PPIs)之间存在相互作用。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。材料与方法本研究使用了法国国家医疗保健数据库中 2011 年 1 月 1 日至 2021 年 12 月 31 日的数据。我们确定了以下患者(i) 年龄等于或大于 18 岁;(ii) 罹患肺癌;(iii) 至少报销过一次以下药物中的一种:厄洛替尼、吉非替尼、阿法替尼和奥西莫替尼。患者的随访时间为 PKI 首次报销日期至 2021 年 12 月 31 日,如果患者死亡,则以死亡日期为准。PKI治疗期间PPI的累积暴露时间按PKI和PPI同时暴露天数与PKI暴露天数之比计算。结果在我们的研究中,34,048 名患者至少接受了一次相关 PKI 的治疗:26,133 人(76.8%)接受了厄洛替尼;3,142 人(9.2%)接受了吉非替尼;1,417 人(4.2%)接受了阿法替尼;3,356 人(9.9%)接受了奥希替尼。与其他患者相比,在20%或更长的PKI治疗期间同时暴露于PKI-PPI相互作用的患者死亡风险更高(HR,1.60 [95 % CI,1.57-1.64])。讨论/结论在我们的研究中,观察到暴露于PKI-PPI相互作用的患者死亡风险升高。最后,我们确定了这种相互作用的剂量依赖效应。奥希替尼和PPI的这种有害效应首次在现实生活中被揭示出来。
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Deleterious association between proton pump inhibitor and protein kinase inhibitor exposure and survival for patients with lung cancer: A nationwide cohort study

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.

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来源期刊
CiteScore
4.30
自引率
0.00%
发文量
148
审稿时长
56 days
期刊介绍: Cancer Treatment and Research Communications is an international peer-reviewed publication dedicated to providing comprehensive basic, translational, and clinical oncology research. The journal is devoted to articles on detection, diagnosis, prevention, policy, and treatment of cancer and provides a global forum for the nurturing and development of future generations of oncology scientists. Cancer Treatment and Research Communications publishes comprehensive reviews and original studies describing various aspects of basic through clinical research of all tumor types. The journal also accepts clinical studies in oncology, with an emphasis on prospective early phase clinical trials. Specific areas of interest include basic, translational, and clinical research and mechanistic approaches; cancer biology; molecular carcinogenesis; genetics and genomics; stem cell and developmental biology; immunology; molecular and cellular oncology; systems biology; drug sensitivity and resistance; gene and antisense therapy; pathology, markers, and prognostic indicators; chemoprevention strategies; multimodality therapy; cancer policy; and integration of various approaches. Our mission is to be the premier source of relevant information through promoting excellence in research and facilitating the timely translation of that science to health care and clinical practice.
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