Bernsen Emma C, Hogenes Valery J, Nuijen Bastiaan, Hanff Lidwien M, Huitema Alwin D R, Diekstra Meta H M
Princess Máxima Center for Pediatric Oncology, Department of Pharmacology, Heidelberglaan 25, 3584 CS Utrecht, The Netherlands.
Department of Pharmacy & Pharmacology, The Netherlands Cancer Institute-Antoni van Leeuwenhoek, Plesmanlaan 121, 1066 CX Amsterdam, The Netherlands.
Pharmaceutics. 2022 Dec 17;14(12):2834. doi: 10.3390/pharmaceutics14122834.
Over 75 kinase inhibitors (KIs) have been approved for the treatment of various cancers. KIs are orally administrated but mostly lack pediatric age-appropriate dosage forms or instructions for dose manipulation. This is highly problematic for clinical practice in pediatric oncology, as flexible oral formulations are essential to individually set dosages and to adjust it to a child's swallowability. Most KIs are poorly soluble, categorized in Biopharmaceutics Classification System (BCS) class II or IV, and improperly manipulating the KI formulation can alter pharmacokinetics and jeopardize KI drug safety and efficacy. Therefore, the goals of this review were to provide practical recommendations for manipulating the formulation of the 15 most frequently used KIs in pediatric oncology (i.e., bosutinib, cabozantinib, cobimetinib, crizotinib, dabrafenib, dasatinib, entrectinib, imatinib, larotrectinib, nilotinib, ponatinib, ruxolitinib, selumetinib, sunitinib and trametinib) based on available literature studies and fundamental drug characteristics and to establish a decision tool that supports decisions regarding formulation manipulation of solid oral dosages of KIs that have been or will be licensed (for adult and/or pediatric cancers) but are not included in this review.
超过75种激酶抑制剂(KIs)已被批准用于治疗各种癌症。激酶抑制剂通过口服给药,但大多缺乏适合儿科年龄段的剂型或剂量调整说明。这对于儿科肿瘤学的临床实践来说是个大问题,因为灵活的口服制剂对于根据个体情况设定剂量以及根据儿童的吞咽能力进行调整至关重要。大多数激酶抑制剂的溶解度较差,属于生物药剂学分类系统(BCS)中的II类或IV类,不恰当地处理激酶抑制剂的制剂会改变药代动力学,并危及激酶抑制剂药物的安全性和有效性。因此,本综述的目的是根据现有文献研究和基本药物特性,为儿科肿瘤学中15种最常用的激酶抑制剂(即博舒替尼、卡博替尼、考比替尼、克唑替尼、达拉非尼、达沙替尼、恩曲替尼、伊马替尼、拉罗替尼、尼洛替尼、泊那替尼、鲁索替尼、司美替尼、舒尼替尼和曲美替尼)的制剂处理提供实用建议,并建立一个决策工具,以支持对已获许可(用于成人和/或儿科癌症)但未纳入本综述的固体口服剂型激酶抑制剂的制剂处理决策。