DMPK, Oncology, IMED Biotech Unit, AstraZeneca, Cambridge, UK.
DMPK, Asia IMED, IMED Biotech Unit, AstraZeneca, Shanghai, China.
Drug Discov Today. 2019 May;24(5):1067-1073. doi: 10.1016/j.drudis.2019.01.015. Epub 2019 Jan 30.
Due to the blood-brain barrier (BBB) limiting the exposure of therapeutics to the central nervous system (CNS), patients with brain malignancies are challenging to treat, typically have poor prognoses, and represent a significant unmet medical need. Preclinical data report osimertinib to have significant BBB penetration and emerging clinical data demonstrate encouraging activity against CNS malignancies. Here, we discuss the oncology drug candidates AZD3759 and AZD1390 as case examples of discovery projects designing in BBB penetrance. We demonstrate how these innovative kinase inhibitors were recognized as brain penetrant and outline our view of experimental approaches and strategies that can facilitate the discovery of new brain-penetrant therapies for the treatment of primary and secondary CNS malignancies as well as other CNS disorders.
由于血脑屏障(BBB)限制了治疗药物在中枢神经系统(CNS)中的暴露,患有脑部恶性肿瘤的患者治疗难度大,预后通常较差,存在显著的未满足的医疗需求。临床前数据报告奥希替尼具有显著的 BBB 穿透性,而新兴的临床数据显示对 CNS 恶性肿瘤具有令人鼓舞的活性。在这里,我们将 AZD3759 和 AZD1390 这两种肿瘤候选药物作为发现项目设计 BBB 穿透性的案例进行讨论。我们展示了这些创新性激酶抑制剂如何被识别为具有脑穿透性,并概述了我们对实验方法和策略的看法,这些方法和策略可以促进新的脑穿透性疗法的发现,以治疗原发性和继发性 CNS 恶性肿瘤以及其他 CNS 疾病。