| Literature DB >> 33800821 |
Antonio D'Ammando1, Luca Raspagliesi1,2,3, Matteo Gionso1,4, Andrea Franzini5, Edoardo Porto2,3, Francesco Di Meco2,3,6, Giovanni Durando7, Serena Pellegatta8, Francesco Prada1,9,10.
Abstract
High-grade gliomas are the most common and aggressive malignant primary brain tumors. Current therapeutic schemes include a combination of surgical resection, radiotherapy and chemotherapy; even if major advances have been achieved in Progression Free Survival and Overall Survival for patients harboring high-grade gliomas, prognosis still remains poor; hence, new therapeutic options for malignant gliomas are currently researched. Sonodynamic Therapy (SDT) has proven to be a promising treatment combining the effects of low-intensity ultrasound waves with various sound-sensitive compounds, whose activation leads to increased immunogenicity of tumor cells, increased apoptotic rates and decreased angiogenetic potential. In addition, this therapeutic technique only exerts its cytotoxic effects on tumor cells, while both ultrasound waves and sensitizing compound are non-toxic per se. This review summarizes the present knowledge regarding mechanisms of action of SDT and currently available sonosensitizers and focuses on the preclinical and clinical studies that have investigated its efficacy on malignant gliomas. To date, preclinical studies implying various sonosensitizers and different treatment protocols all seem to confirm the anti-tumoral properties of SDT, while first clinical trials will soon start recruiting patients. Accordingly, it is crucial to conduct further investigations regarding the clinical applications of SDT as a therapeutic option in the management of intracranial gliomas.Entities:
Keywords: 5-aminolevulinic acid; cavitation; fluorescein; gliomas; sonodynamic therapy
Year: 2021 PMID: 33800821 PMCID: PMC7961476 DOI: 10.3390/jcm10051101
Source DB: PubMed Journal: J Clin Med ISSN: 2077-0383 Impact factor: 4.241