Genentech, South San Francisco, California.
Neuro Oncol. 2018 Feb 19;20(3):307-312. doi: 10.1093/neuonc/nox179.
Despite biological rationale and significant clinical study, the pursuit of small-molecule kinase inhibitors for the treatment of brain cancers has had very limited success. This Advance-in-Brief discusses the need for drugs to achieve free brain penetration to engage their targets where CNS tumors reside. This need to achieve free, as opposed to total, drug concentrations in the brain may be a contributing factor to why so many small-molecule kinase inhibitors have not realized success in the neuro-oncology setting. For kinase targets of interest for brain cancer, either the vast majority of small-molecule inhibitors have data suggesting that free brain penetration would be limited or there are inadequate data to suggest that free brain penetration could be expected. Therefore, kinase targets of interest in the treatment of brain cancers may be inadequately assessed due to a lack of freely brain-penetrant inhibitors available for clinical study. Encouraging recent drug discovery efforts that focused on achieving free brain penetration for cancers in the CNS are highlighted. Still, further efforts are needed to enable thorough clinical evaluation of biological hypotheses.
尽管具有生物学依据和大量临床研究,但小分子激酶抑制剂在治疗脑癌方面的应用非常有限。本文简要讨论了药物需要穿透血脑屏障以到达中枢神经系统肿瘤所在部位的靶点,实现自由穿透,而不是总浓度,这可能是许多小分子激酶抑制剂在神经肿瘤学环境中未能取得成功的原因之一。对于脑癌相关的激酶靶点,要么绝大多数小分子抑制剂的数据表明自由脑穿透将受到限制,要么没有足够的数据表明可以预期自由脑穿透。因此,由于缺乏可供临床研究的可自由穿透脑的抑制剂,脑癌治疗中感兴趣的激酶靶点可能评估不足。本文强调了最近药物研发工作的重点是为中枢神经系统癌症实现自由脑穿透。尽管如此,仍需要进一步努力,以能够对生物学假说进行全面的临床评估。