Department of Neurosurgery, Brigham and Women's Hospital, Boston, Massachusetts.
Harvard Medical School, Harvard University, Boston, Massachusetts.
Oper Neurosurg (Hagerstown). 2020 Jul 1;19(1):9-18. doi: 10.1093/ons/opz374.
A key challenge in the medical treatment of brain tumors is the limited penetration of most chemotherapeutic agents across the blood-brain barrier (BBB) into the tumor and the infiltrative margin around the tumor. Magnetic resonance-guided focused ultrasound (MRgFUS) is a promising tool to enhance the delivery of chemotherapeutic agents into brain tumors.
To review the mechanism of FUS, preclinical evidence, and clinical studies that used low-frequency FUS for a BBB opening in gliomas.
Literature review.
The potential of externally delivered low-intensity ultrasound for a temporally and spatially precise and predictable disruption of the BBB has been investigated for over a decade, yielding extensive preclinical literature demonstrating that FUS can disrupt the BBB in a spatially targeted and temporally reversible manner. Studies in animal models documented that FUS enhanced the delivery of numerous chemotherapeutic and investigational agents across the BBB and into brain tumors, including temozolomide, bevacizumab, 1,3-bis (2-chloroethyl)-1-nitrosourea, doxorubicin, viral vectors, and cells. Chemotherapeutic interventions combined with FUS slowed tumor progression and improved animal survival. Recent advances of MRgFUS systems allow precise, temporally and spatially controllable, and safe transcranial delivery of ultrasound energy. Initial clinical evidence in glioma patients has shown the efficacy of MRgFUS in disrupting the BBB, as demonstrated by an enhanced gadolinium penetration.
Thus far, a temporary disruption of the BBB followed by the administration of chemotherapy has been both feasible and safe. Further studies are needed to determine the actual drug delivery, including the drug distribution at a tissue-level scale, as well as effects on tumor growth and patient prognosis.
在脑瘤的治疗中,一个关键的挑战是大多数化疗药物通过血脑屏障(BBB)进入肿瘤和肿瘤周围浸润边缘的能力有限。磁共振引导聚焦超声(MRgFUS)是一种有前途的工具,可以增强化疗药物进入脑肿瘤的递送。
综述 FUS 的作用机制、临床前证据和临床研究,这些研究使用低频 FUS 打开脑胶质瘤的 BBB。
文献回顾。
十多年来,人们一直在研究外部传递的低强度超声对 BBB 的时间和空间精确、可预测的破坏的潜力,产生了广泛的临床前文献,证明 FUS 可以以空间靶向和时间可逆的方式破坏 BBB。动物模型研究表明,FUS 增强了许多化疗药物和研究药物通过 BBB 进入脑肿瘤的递送,包括替莫唑胺、贝伐单抗、1,3-双(2-氯乙基)-1-亚硝脲、多柔比星、病毒载体和细胞。化疗干预与 FUS 联合使用可减缓肿瘤进展并提高动物生存率。MRgFUS 系统的最新进展允许精确、时间和空间可控、安全的颅穿透超声能量传递。初步的临床证据表明,MRgFUS 在破坏 BBB 方面是有效的,如增强的钆渗透所证明的那样。
到目前为止,BBB 的暂时破坏,随后进行化疗,是可行且安全的。需要进一步研究来确定实际的药物递送,包括药物在组织水平上的分布,以及对肿瘤生长和患者预后的影响。