Experimental and Clinical Pharmacology Unit, Centro di Riferimento Oncologico (CRO), IRCCS, 33081 Aviano, Italy.
Department of Oncology and Hemato-Oncology, Università degli Studi di Milano, 20122 Milan, Italy.
Int J Mol Sci. 2020 Sep 1;21(17):6350. doi: 10.3390/ijms21176350.
Palbociclib, ribociclib, and abemaciclib belong to the third generation of cyclin-dependent kinases inhibitors (CDKis), an established therapeutic class for advanced and metastatic breast cancer. Interindividual variability in the therapeutic response of CDKis has been reported and some individuals may experience increased and unexpected toxicity. This narrative review aims at identifying the factors potentially concurring at this variability for driving the most appropriate and tailored use of CDKis in the clinic. Specifically, concomitant medications, pharmacogenetic profile, and pathophysiological conditions could influence absorption, distribution, metabolism, and elimination pharmacokinetics. A personalized therapeutic approach taking into consideration all factors potentially contributing to an altered pharmacokinetic/pharmacodynamic profile could better drive safe and effective clinical use.
帕博西尼、瑞博西尼和阿贝西利属于第三代细胞周期蛋白依赖性激酶抑制剂(CDKis),是晚期和转移性乳腺癌的一种成熟治疗类别。已经报道了 CDKis 治疗反应的个体间变异性,一些个体可能会经历增加和意外的毒性。本叙述性综述旨在确定潜在的因素,这些因素可能会影响 CDKis 在临床上的最佳和个体化使用。具体而言,伴随药物、药物遗传学特征和病理生理状况可能会影响吸收、分布、代谢和消除药代动力学。考虑到所有可能导致药代动力学/药效学特征改变的因素的个性化治疗方法可以更好地推动安全有效的临床应用。