帕唑帕尼和抗酸药:来自世卫组织药物警戒数据库的见解。

IF 2.7 4区 医学 Q3 ONCOLOGY
Kazuki Nishida, Yao Liang, Osamu Maeda, Angélique Da Silva, Yuichi Ando, Basile Chrétien
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引用次数: 0

摘要

Pazopanib是一种多靶点酪氨酸激酶抑制剂,用于晚期肾细胞癌和软组织肉瘤。然而,它与剂量依赖性不良事件(ae)相关,包括高血压和胃肠道问题。抗酸剂如质子泵抑制剂(PPIs)和组胺-2受体拮抗剂(H2RAs)通常同时使用,这引起了对潜在药物相互作用的担忧。帕唑帕尼的溶解度和吸收与pH值有关,胃pH值升高可能会降低其生物利用度。在这项研究中,我们使用多变量logistic回归模型分析了VigiBase®数据,发现pazopanib和抗酸剂(PPIs, H2RAs等)之间存在显著的相互作用,表明严重AE报告减少,可能是由于pazopanib暴露量较低。对CYP3A4抑制剂的二次分析显示,严重ae发生率偏高的趋势不显著,与预期的药代动力学效应一致。这些发现强调当抗酸药与帕唑帕尼联合使用时需要谨慎,因为它可能会降低毒性和疗效。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pazopanib and antacids: insights from the WHO pharmacovigilance database.

Pazopanib, a multi-targeted tyrosine kinase inhibitor, is used for advanced renal cell carcinoma and soft tissue sarcoma. However, it is associated with dose-dependent adverse events (AEs), including hypertension, and gastrointestinal issues. Antacids like proton pump inhibitors (PPIs) and histamine-2 receptor antagonists (H2RAs) are often co-administered, raising concerns about potential drug interactions. Pazopanib's solubility and absorption are pH-dependent, with increased gastric pH potentially reducing its bioavailability. In this study, we analyzed VigiBase® data using multivariate logistic regression models and found significant interactions between pazopanib and antacids (PPIs, H2RAs, and others), suggesting reduced serious AE reporting, possibly due to lower pazopanib exposure. A secondary analysis of CYP3A4 inhibitors showed a non-significant trend for higher serious AEs, aligning with expected pharmacokinetic effects. These findings emphasize the need for caution when combining antacids with pazopanib, as it may reduce both toxicity and efficacy.

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来源期刊
CiteScore
6.10
自引率
3.30%
发文量
116
审稿时长
2.5 months
期刊介绍: Addressing a wide range of pharmacologic and oncologic concerns on both experimental and clinical levels, Cancer Chemotherapy and Pharmacology is an eminent journal in the field. The primary focus in this rapid publication medium is on new anticancer agents, their experimental screening, preclinical toxicology and pharmacology, single and combined drug administration modalities, and clinical phase I, II and III trials. It is essential reading for pharmacologists and oncologists giving results recorded in the following areas: clinical toxicology, pharmacokinetics, pharmacodynamics, drug interactions, and indications for chemotherapy in cancer treatment strategy.
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