Sprowls Samuel A, Arsiwala Tasneem A, Bumgarner Jacob R, Shah Neal, Lateef Sundus S, Kielkowski Brooke N, Lockman Paul R
Department of Pharmaceutical Sciences, School of Pharmacy, West Virginia University HSC, Morgantown, West Virginia 26506, USA.
Department of Pharmaceutical Sciences, School of Pharmacy, West Virginia University HSC, Morgantown, West Virginia 26506, USA.
Trends Cancer. 2019 Aug;5(8):495-505. doi: 10.1016/j.trecan.2019.06.003. Epub 2019 Jul 20.
Brain metastases encompass nearly 80% of all intracranial tumors. A late stage diagnosis confers a poor prognosis, with patients typically surviving less than 2 years. Poor survival can be equated to limited effective treatment modalities. One reason for the failure rates is the presence of the blood-brain barrier (BBB) and blood-tumor barrier (BTB) that limit the access of potentially effective chemotherapeutics to metastatic lesions. Strategies to overcome these barriers include new small molecule entities capable of crossing into the brain parenchyma, novel formulations of existing chemotherapies, and disruptive techniques. Here, we review BBB physiology and BTB pathophysiology. Additionally, we review the limitations of routinely practiced therapies and three current methods being explored for BBB/BTB disruption for improved delivery of chemotherapy to brain tumors.
脑转移瘤占所有颅内肿瘤的近80%。晚期诊断预示着预后不良,患者通常存活时间不到2年。生存期短可归因于有效的治疗方式有限。治疗失败率高的一个原因是血脑屏障(BBB)和血肿瘤屏障(BTB)的存在,它们限制了潜在有效化疗药物进入转移病灶。克服这些屏障的策略包括能够进入脑实质的新型小分子实体、现有化疗药物的新型制剂以及破坏性技术。在此,我们综述血脑屏障的生理学和血肿瘤屏障的病理生理学。此外,我们还综述了常规治疗方法的局限性以及目前正在探索的三种用于破坏血脑屏障/血肿瘤屏障以改善化疗药物向脑肿瘤递送的方法。