Journal
JOURNAL OF NEURO-ONCOLOGY
Volume 156, Issue 1, Pages 33-48Publisher
SPRINGER
DOI: 10.1007/s11060-021-03837-0
Keywords
Biomarkers; Focused Ultrasound; Gliomas; Liquid biopsy; Review
Categories
Funding
- NINDS [5R25NS065729, 1R21NS113016-01]
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Despite current limitations in detecting brain tumor biomarkers in blood or cerebrospinal fluid, disrupting the blood-brain barrier with MRI-guided focused ultrasound (MRgFUS) shows promise in enhancing the presence of these biomarkers. The non-invasive nature of liquid biopsies can provide valuable insights into tumor evolution and treatment response, offering new possibilities for future management of brain tumor patients.
Introduction Despite advances in modern medicine, brain tumor patients are still monitored purely by clinical evaluation and imaging. Traditionally, invasive strategies such as open or stereotactic biopsies have been used to confirm the etiology of clinical and imaging changes. Liquid biopsies can enable physicians to noninvasively analyze the evolution of a tumor and a patient's response to specific treatments. However, as a consequence of biology and the current limitations in detection methods, no blood or cerebrospinal fluid (CSF) brain tumor-derived biomarkers are used in routine clinical practice. Enhancing the presence of tumor biomarkers in blood and CSF via brain-blood barrier (BBB) disruption with MRI-guided focused ultrasound (MRgFUS) is a very compelling strategy for future management of brain tumor patients. Methods A literature review on MRgFUS-enabled brain tumor liquid biopsy was performed using Medline/Pubmed databases and clinical trial registries. Results The therapeutic applications of MRgFUS to target brain tumors have been under intense investigation. At high-intensity, MRgFUS can ablate brain tumors and target tissues, which needs to be balanced with the increased risk for damage to surrounding normal structures. At lower-intensity and pulsed-frequency, MRgFUS may be able to disrupt the BBB transiently. Thus, while facilitating intratumoral or parenchymal access to standard or novel therapeutics, BBB disruption with MRgFUS has opened the possibility of enhanced detection of brain tumor-derived biomarkers. Conclusions In this review, we describe the concept of MRgFUS-enabled brain tumor liquid biopsy and present the available preclinical evidence, ongoing clinical trials, limitations, and future directions of this application.
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