Department of Neurosurgery, University of Maryland School of Medicine , Baltimore, MD , USA ; Department of Anatomy and Neurobiology, University of Maryland School of Medicine , Baltimore, MD , USA.
Department of Neurosurgery, Pathology and Immunology, Center for Human Immunology and Immunotherapy Programs, Washington University School of Medicine , St. Louis, MO , USA.
Front Oncol. 2014 Jul 21;4:126. doi: 10.3389/fonc.2014.00126. eCollection 2014.
There is great promise that ongoing advances in the delivery of therapeutics to the central nervous system (CNS) combined with rapidly expanding knowledge of brain tumor patho-biology will provide new, more effective therapies. Brain tumors that form from brain cells, as opposed to those that come from other parts of the body, rarely metastasize outside of the CNS. Instead, the tumor cells invade deep into the brain itself, causing disruption in brain circuits, blood vessel and blood flow changes, and tissue swelling. Patients with the most common and deadly form, glioblastoma (GBM) rarely live more than 2 years even with the most aggressive treatments and often with devastating neurological consequences. Current treatments include maximal safe surgical removal or biopsy followed by radiation and chemotherapy to address the residual tumor mass and invading tumor cells. However, delivering effective and sustained treatments to these invading cells without damaging healthy brain tissue is a major challenge and focus of the emerging fields of nanomedicine and viral and cell-based therapies. New treatment strategies, particularly those directed against the invasive component of this devastating CNS disease, are sorely needed. In this review, we (1) discuss the history and evolution of treatments for GBM, (2) define and explore three critical barriers to improving therapeutic delivery to invasive brain tumors, specifically, the neuro-vascular unit as it relates to the blood brain barrier, the extra-cellular space in regard to the brain penetration barrier, and the tumor genetic heterogeneity and instability in association with the treatment efficacy barrier, and (3) identify promising new therapeutic delivery approaches that have the potential to address these barriers and create sustained, meaningful efficacy against GBM.
有很大的希望,中枢神经系统 (CNS) 治疗方法的不断进步,加上对脑肿瘤病理生物学的快速扩展的认识,将提供新的、更有效的治疗方法。源自脑细胞的脑肿瘤与源自身体其他部位的肿瘤不同,很少在 CNS 之外转移。相反,肿瘤细胞侵入大脑深处,导致大脑回路中断、血管和血流变化以及组织肿胀。最常见和最致命的形式——胶质母细胞瘤 (GBM) 的患者,即使采用最激进的治疗方法,也很少能活过 2 年,而且常常会带来毁灭性的神经后果。目前的治疗方法包括最大限度的安全手术切除或活检,然后进行放疗和化疗,以解决残余肿瘤和侵袭性肿瘤细胞。然而,在不损害健康脑组织的情况下,向这些侵袭性细胞提供有效和持续的治疗是一个主要挑战,也是新兴的纳米医学、病毒和细胞治疗领域的重点。迫切需要新的治疗策略,特别是针对这种毁灭性 CNS 疾病侵袭性成分的策略。在这篇综述中,我们 (1) 讨论了 GBM 治疗的历史和演变,(2) 定义并探讨了改善侵袭性脑肿瘤治疗药物传递的三个关键障碍,特别是与血脑屏障相关的神经血管单元、与脑渗透障碍相关的细胞外空间,以及与治疗效果障碍相关的肿瘤遗传异质性和不稳定性,(3) 确定了有前途的新治疗药物传递方法,这些方法有可能克服这些障碍,并对 GBM 产生持续、有意义的疗效。