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Towards controlled drug delivery in brain tumors with microbubble-enhanced focused ultrasound.

Authors: Schoen S, Kilinc MS, Lee H, Guo Y, Degertekin FL, Woodworth GF, Arvanitis C

Brain tumors are particularly challenging malignancies, due to their location in a structurally and functionally distinct part of the human body - the central nervous system (CNS). The CNS is separated and protected by a unique system of brain and blood vessel cells which together prevent most bloodborne therapeutics from entering the brain tumor microenvironment (TME). Recently, great strides have been made through microbubble (MB) ultrasound contrast agents in conjunction with ultrasound energy to locally increase the permeability of brain vessels and modulate the brain TME. As we elaborate in this review, this physical method can effectively deliver a wide range of anticancer agents, including chemotherapeutics, antibodies, and nanoparticle drug conjugates across a range of preclinical brain tumors, including high grade glioma (glioblastoma), diffuse intrinsic pontine gliomas, and brain metastasis. Moreover, recent evidence suggests that this technology can promote the effective delivery of novel immunotherapeutic agents, including immune check-point inhibitors and chimeric antigen receptor T cells, among others. With early clinical studies demonstrating safety, and several Phase I/II trials testing the preclinical findings underway, this technology is making firm steps towards shaping the future treatments of primary and metastatic brain cancer. By elaborating on its key components, including ultrasound systems and MB technology, along with methods for closed-loop spatial and temporal control of MB activity, we highlight how this technology can be tuned to enable new, personalized treatment strategies for primary brain malignancies and brain metastases.

Introduction

Purpose Drug delivery with BBB opening
Study Objective To review how microbubble ultrasound-mediated modulation of the blood–brain barrier can enhance delivery of anticancer and immunotherapeutic agents to brain tumors and to discuss the underlying technologies, control methods, and clinical translation.
Disease model Brain tumors (glioma — including glioblastoma and diffuse intrinsic pontine glioma; and brain metastasis)
Cargo name and characteristics Chemotherapeutics (small-molecule anticancer drugs), antibodies including immune checkpoint inhibitors (protein biologics/monoclonal antibodies), nanoparticle drug conjugates (nanoparticles carrying therapeutic payloads), and chimeric antigen receptor (CAR) T cells (cellular immunotherapy)

Outcomes and Safety

Summary of Outcomes Microbubble-enhanced focused ultrasound noninvasively increased blood–brain barrier permeability, improving delivery of chemotherapies, antibodies, nanoparticles and immunotherapies to preclinical brain tumors and modulating the tumor microenvironment with early clinical studies showing safety. The review highlights successful strategies of tuning ultrasound systems and microbubble formulations using closed-loop spatial and temporal control of microbubble activity, though no specific numerical ultrasound parameter set is reported.
Safety-related matter Early clinical studies demonstrated safety; no adverse effects were reported in the provided excerpt.

Brain Region

Visualization unavailable

Ultrasound Parameters

Focal Characteristics Focal depth: None; Focal length: None; Aperture size: None

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