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Focused Ultrasound Strategies for Brain Tumor Therapy.

Authors: Bunevicius A, McDannold NJ, Golby AJ

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.

Introduction

Purpose Drug delivery with BBB opening
Study Objective To review the mechanism, preclinical evidence, and clinical studies of low-frequency focused ultrasound for opening the blood–brain barrier in gliomas.
Animal model / Human subject Not applicable (literature review; no experimental organism reported)
Disease model glioma
MRI or image guidance method Magnetic resonance-guided focused ultrasound (MRgFUS)
Targeted brain region(s) Blood–Brain Barrier (Bbb) In Gliomas (Tumor And Infiltrative Margin)
Target coordinates not reported
Cargo name and characteristics Temozolomide — small‑molecule oral alkylating chemotherapeutic; Bevacizumab — protein biologic (monoclonal antibody, anti‑VEGF); 1,3‑bis(2‑chloroethyl)‑1‑nitrosourea (BCNU) — small‑molecule nitrosourea alkylating chemotherapeutic; Doxorubicin — small‑molecule anthracycline chemotherapeutic; Viral vectors — gene delivery vehicles (viral vector platforms); Cells — cellular therapeutic/ cell delivery; Gadolinium — MRI contrast agent (small‑molecule chelate used to assess BBB opening).
Route of administration Systemic administration (e.g., intravenous or oral chemotherapy) combined with transcranial MR-guided focused ultrasound (MRgFUS)–mediated temporary blood–brain barrier disruption

Outcomes and Safety

Summary of Outcomes Low-intensity MR-guided focused ultrasound transiently and locally opens the blood–brain barrier to enhance delivery of chemotherapeutics and vectors into gliomas, slowing tumor progression and improving survival in animal models and demonstrating safe increased drug penetration in early human studies.
Duration of biological effect Not specified
Safety-related matter The review states that MRgFUS-mediated temporary BBB disruption followed by chemotherapy has been feasible and safe in preclinical and initial clinical studies, with no adverse effects reported in this text.

Brain Region

Ultrasound Parameters

Ultrasound instrument Not specified in text
FUS Frequency Not specified in the provided text
FUS Intensity Not specified in the provided text
FUS Pressure Not reported
FUS Mode not specified
Pulse duration not reported
Duration of a single FUS session Not reported in the paper
Focal Characteristics Not specified
Treatment frequency Multiple sessions

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