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用于治疗黑色素瘤的丝裂原活化蛋白激酶 (MEK) 抑制剂的潜在药物相互作用。

Potential drug-drug interactions with mitogen-activated protein kinase (MEK) inhibitors used to treat melanoma.

机构信息

Dermatologic Clinic, Department of Clinical and Molecular Sciences, Ancona, Marche, Italy.

出版信息

Expert Opin Drug Metab Toxicol. 2023 Jul-Dec;19(8):555-567. doi: 10.1080/17425255.2023.2255519. Epub 2023 Sep 6.

Abstract

INTRODUCTION

The management of patients with BRAF-mutated advanced melanoma who are undergoing targeted therapy with MEK inhibitors can be complicated by the co-administration of multiple medications, which can give rise to drug-drug interactions of clinical significance.

COVERED AREAS

Our review presents a comprehensive analysis of the pharmacokinetic and pharmacodynamic interactions of the three approved for advanced melanoma MEK inhibitor drugs - binimetinib, cobimetinib, and trametinib. MEDLINE (PubMed) was utilized for the literature search, comprising clinical studies, observational studies, and preclinical research. The review discusses the impact of these interactions on efficacy and safety of the treatments and differentiates between interactions supported by pharmacokinetic or pharmacodynamic mechanisms, those encountered in clinical practice, and those observed in preclinical studies.

EXPERT OPINION

Physicians should be aware about potential benefits, but also increased toxicity caused by drug interactions between MEK inhibitors and other drugs in the management of patients with metastatic melanoma.

摘要

简介

接受 MEK 抑制剂靶向治疗的 BRAF 突变型晚期黑色素瘤患者的管理可能因同时使用多种药物而变得复杂,这些药物可能会产生具有临床意义的药物相互作用。

涵盖领域

我们的综述对三种已批准用于晚期黑色素瘤的 MEK 抑制剂药物——binimetinib、cobimetinib 和 trametinib 的药代动力学和药效学相互作用进行了全面分析。利用 MEDLINE(PubMed)进行文献检索,包括临床研究、观察性研究和临床前研究。该综述讨论了这些相互作用对治疗效果和安全性的影响,并区分了基于药代动力学或药效学机制的相互作用、临床实践中遇到的相互作用以及临床前研究中观察到的相互作用。

专家意见

医生应该意识到,在管理转移性黑色素瘤患者时,MEK 抑制剂与其他药物之间的药物相互作用可能会带来潜在的益处,但也会增加毒性。

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