Can Focused Ultrasound Overcome the Failure of Chemotherapy in Treating Pediatric Diffuse Intrinsic Pontine Glioma Due to a Blood-Brain Barrier Obstacle?
Authors: Filieri S, Miciaccia M, Armenise D, Baldelli OM, Liturri A, Ferorelli S, Sardanelli AM, Perrone MG, Scilimati A
<b>Background</b>: The blood-brain barrier (BBB) plays an important role in regulating homeostasis of the central nervous system (CNS), and it is an obstacle for molecules with a molecular weight higher than 500 Da seeking to reach it, making many drugs ineffective simply because they cannot be delivered to where they are needed. As a result, crossing the BBB remains the rate-limiting factor in brain drug delivery during the treatment of brain diseases, specifically tumors such as diffuse intrinsic pontine glioma (DIPG), a highly aggressive pediatric tumor with onset in the pons Varolii, the middle portion of the three contiguous parts of the brainstem, located above the medulla and below the midbrain. <b>Methods</b>: Currently, radiotherapy (RT) relieves DIPG symptoms but chemotherapy drugs do not lead to significant results as they do not easily cross the BBB. Focused ultrasound (FUS) and microbubbles (MBs) can temporarily open the BBB, facilitating radiotherapy and the entry of drugs into the CNS. A patient-derived xenograft DIPG model exposed to high-intensity focalized ultrasound (HIFU) or low-intensity focalized ultrasound (LIFU) combined with MBs was treated with doxorubicin, panobinostat, olaparib, ONC201 (Dordaviprone<sup>®</sup>) and anti-PD1. Panobinostat has also been used in children with diffuse midline glioma, a broad class of brain tumors to which DIPG belongs. <b>Results</b>: Preliminary studies were performed using FUS to temporarily open the BBB and allow a milder use of radiotherapy and facilitate the passage of drugs through the BBB. The data collected show that after opening the BBB with FUS and MBs, drug delivery to the CNS significantly improved. <b>Conclusions</b>: FUS associated with MBs appears safe and feasible and represents a new strategy to increase the uptake of drugs in the CNS and therefore enhance their effectiveness. This review reports pre-clinical and clinical studies performed to demonstrate the usefulness of FUS in patients with DIPG treated with some chemotherapy. The papers reviewed were published in PubMed until the end of 2024 and were found using a combination of the following keywords: diffuse intrinsic pontine glioma (DIPG), DIPG H3K27-altered, blood-brain barrier and BBB, focused ultrasound (FUS) and radiotherapy (RT).
Introduction
Purpose
Drug delivery with BBB opening
Study Objective
To evaluate whether focused ultrasound combined with microbubbles can safely and effectively open the blood–brain barrier to enhance delivery and efficacy of chemotherapeutic agents and radiotherapy in diffuse intrinsic pontine glioma (DIPG).
Disease model
Diffuse intrinsic pontine glioma (DIPG)
Targeted brain region(s)
Pons
Cargo name and characteristics
Doxorubicin (small-molecule chemotherapeutic, anthracycline); Panobinostat (small-molecule HDAC inhibitor); Olaparib (small-molecule PARP inhibitor); ONC201 / Dordaviprone® (small-molecule imipridone anticancer agent); Anti-PD1 (monoclonal antibody, protein biologic)
Outcomes and Safety
Summary of Outcomes
Focused ultrasound (FUS) combined with microbubbles transiently opens the blood–brain barrier in DIPG models, significantly increasing CNS delivery of multiple chemotherapeutics (e.g., doxorubicin, panobinostat, olaparib, ONC201) and potentially allowing reduced radiotherapy; both high‑intensity focalized ultrasound (HIFU + MBs) and low‑intensity focalized ultrasound (LIFU + MBs) were tested and reported as effective and feasible.
Safety-related matter
Focused ultrasound (FUS) with microbubbles (MBs) appears safe and feasible; no adverse effects were reported in the reviewed pre-clinical and clinical studies.
Brain Region
Ultrasound Parameters
Focal Characteristics
focal depth: None; focal length: None; aperture size: None
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