Department of Pharmacy & Pharmacology, Antoni van Leeuwenhoek/Netherlands Cancer Institute, Amsterdam, The Netherlands.
Department of Clinical Pharmacology, Division of Medical Oncology, Antoni van Leeuwenhoek/Netherlands Cancer Institute, Amsterdam, The Netherlands.
Clin Pharmacol Ther. 2020 Sep;108(3):494-505. doi: 10.1002/cpt.1808. Epub 2020 Mar 9.
In recent years new targeted small molecule kinase inhibitors have become available for pediatric patients with cancer. Relationships between drug exposure and treatment response have been established for several of these drugs in adults. Following these exposure-response relationships, pharmacokinetic (PK) target minimum plasma rug concentration at the end of a dosing interval (C ) values to guide therapeutic drug monitoring (TDM) in adults have been proposed. Despite the fact that variability in PK may be even larger in pediatric patients, TDM is only sparsely applied in pediatric oncology. Based on knowledge of the PK, mechanism of action, molecular driver, and pathophysiology of the disease, we bridge available data on the exposure-efficacy relationship from adults to children and propose target C values to guide TDM for the pediatric population. Dose adjustments in individual pediatric patients can be based on these targets. Nevertheless, further research should be performed to validate these targets.
近年来,新的针对小儿癌症的靶向小分子激酶抑制剂已经问世。在成人中,已经确定了几种此类药物的药物暴露与治疗反应之间的关系。根据这些暴露-反应关系,提出了药代动力学(PK)目标最小血浆浓度(C)值来指导成人的治疗药物监测(TDM)。尽管在儿科患者中,PK 的变异性可能更大,但 TDM 在儿科肿瘤学中应用甚少。基于对 PK、作用机制、分子驱动和疾病病理生理学的了解,我们将成人的暴露-疗效关系的可用数据应用于儿童,并提出了指导儿科人群 TDM 的目标 C 值。可以根据这些目标调整个体儿科患者的剂量。然而,仍需要进一步的研究来验证这些目标。