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

被引:2
作者
Marani, A. [1 ,2 ]
Gioacchini, H. [1 ]
Paolinelli, M. [1 ]
Offidani, A. [1 ]
Campanati, A. [1 ]
机构
[1] Dermatol Clin, Dept Clin & Mol Sci, Ancona, Marche, Italy
[2] Univ Politecn, Dermatol Clin, Dept Clin & Mol Sci, Ancona, Marche, Italy
关键词
MEK inhibitors; BRAF inhibitors; pharmacokinetics; pharmacodynamics; side-effects; synergistic interactions; RETINAL VEIN OCCLUSION; COMBINATION THERAPY; BRAF INHIBITION; CARCINOMA CELLS; ADVERSE EVENTS; TUMOR-GROWTH; DOUBLE-BLIND; IN-VITRO; TRAMETINIB; COBIMETINIB;
D O I
10.1080/17425255.2023.2255519
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
IntroductionThe 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 areasOur 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 opinionPhysicians 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.
引用
收藏
页码:555 / 567
页数:13
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