Sonodynamic therapy and magnetic resonance-guided focused ultrasound: new therapeutic strategy in glioblastoma

被引:26
作者
Bonosi, Lapo [1 ]
Marino, Silvia [2 ]
Benigno, Umberto Emanuele [1 ]
Musso, Sofia [1 ]
Buscemi, Felice [1 ]
Giardina, Kevin [1 ]
Gerardi, Rosamaria [1 ]
Brunasso, Lara [1 ]
Costanzo, Roberta [1 ]
Iacopino, Domenico Gerardo [1 ]
Maugeri, Rosario [1 ]
机构
[1] Univ Palermo, Sch Med, Dept Biomed Neurosci & Adv Diagnost, Neurosurg Clin,AOUP Paolo Giaccone,Post Grad Resid, I-90127 Palermo, Italy
[2] IRCCS Ctr Neurolesi Bonino Pulejo, Messina, Italy
关键词
Foscused Ultrasound; Gliomas; Glioblastoma; Sonodynamic Therapy; MRgFUS; BLOOD-BRAIN-BARRIER; OF-THE-ART; 5-AMINOLEVULINIC ACID; THERMAL ABLATION; INTRACRANIAL GLIOMA; PROTOPORPHYRIN-IX; TUMOR; APOPTOSIS; CELLS; TEMOZOLOMIDE;
D O I
10.1007/s11060-023-04333-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioblastoma (GB) is one of the most aggressive and difficult-to-treat brain tumors, with a poor prognosis and limited treatment options. In recent years, sonodynamic therapy (SDT) and magnetic resonance focused ultrasound (MRgFUS) have emerged as promising approaches for the treatment of GB. SDT uses ultrasound waves in combination with a sonosensitizer to selectively damage cancer cells, while MRgFUS delivers high-intensity ultrasound waves to precisely target tumor tissue and disrupt the blood-brain barrier to enhance drug delivery. In this review, we explore the potential of SDT as a novel therapeutic strategy for GB. We discuss the principles of SDT, its mechanisms of action, and the preclinical and clinical studies that have investigated its use in Gliomas. We also highlight the challenges, the limitations, and the future perspectives of SDT. Overall, SDT and MRgFUS hold promise as novel and potentially complementary treatment modalities for GB. Further research is needed to optimize their parameters and determine their safety and efficacy in humans, but their potential for selective and targeted tumor destruction makes them an exciting area of investigation in the field of brain cancer therapy.
引用
收藏
页码:219 / 238
页数:20
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