Blood-Brain Barrier Opening in Primary Brain Tumors with Non-invasive MR-Guided Focused Ultrasound: A Clinical Safety and Feasibility Study.
Authors: Mainprize T, Lipsman N, Huang Y, Meng Y, Bethune A, Ironside S, Heyn C, Alkins R, Trudeau M, Sahgal A, Perry J, Hynynen K
The blood-brain barrier (BBB) has long limited therapeutic access to brain tumor and peritumoral tissue. In animals, MR-guided focused ultrasound (MRgFUS) with intravenously injected microbubbles can temporarily and repeatedly disrupt the BBB in a targeted fashion, without open surgery. Our objective is to demonstrate safety and feasibility of MRgFUS BBB opening with systemically administered chemotherapy in patients with glioma in a phase I, single-arm, open-label study. Five patients with previously confirmed or suspected high-grade glioma based on imaging underwent the MRgFUS in conjunction with administration of chemotherapy (n = 1 liposomal doxorubicin, n = 4 temozolomide) one day prior to their scheduled surgical resection. Samples of "sonicated" and "unsonicated" tissue were measured for the chemotherapy by liquid-chromatography-mass spectrometry. Complete follow-up was three months. The procedure was well-tolerated, with no adverse clinical or radiologic events related to the procedure. The BBB within the target volume showed radiographic evidence of opening with an immediate 15-50% increased contrast enhancement on T1-weighted MRI, and resolution approximately 20 hours after. Biochemical analysis of sonicated versus unsonicated tissue suggest chemotherapy delivery is feasible. In this study, we demonstrated transient BBB opening in tumor and peritumor tissue using non-invasive low-intensity MRgFUS with systemically administered chemotherapy was safe and feasible. The characterization of therapeutic delivery and clinical response to this treatment paradigm requires further investigation.
Introduction
Purpose
Drug delivery with BBB opening
Study Objective
To determine the safety and feasibility of transiently opening the blood-brain barrier in peritumor brain tissue using transcranial low-intensity MR-guided focused ultrasound during systemic chemotherapy administration.
Disease model
glioma
MRI or image guidance method
MR-guided (MRgFUS) using the ExAblate Neuro system coupled to a 3T MRI with a stereotactic frame/ultrasound helmet; pre‑sonication T1/T2 MRI for target planning, targets placed at tumor margins via a 3×3 grid aligned with the surgical trajectory, and real‑time acoustic feedback used during sonication.
Targeted brain region(s)
Brain Tumor
Cargo name and characteristics
nanoparticle
Route of administration
intravenous
Outcomes and Safety
Summary of Outcomes
MRgFUS transiently opened the BBB in glioma tissue and increased chemotherapy delivery.
Duration of biological effect
20 h
Safety-related matter
No serious adverse effects reported.
Brain Region
Ultrasound Parameters
Ultrasound instrument
MR-guided focused ultrasound transducer
FUS Frequency
220 kHz
FUS Intensity
not reported
FUS Pressure
not reported
FUS Mode
pulsed
Pulse duration
10 ms
Duration of a single FUS session
450 s
Treatment frequency
single
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