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Dilmanian, F. Avraham

Mayo Clinic

Stony Brook University

Citations 2

Heavy Ion Minibeam Therapy: Side Effects in Normal Brain
Eley, John G. , Haga, Catherine , Lazenby, Ellis M., Raver, Charles , Rusek, A., Dilmanian, F. Avraham, Waddell, Jaylyn , Keller, Asaf , Krishnan, Sunil

Cancers | December 9, 2021 | Volume: 13 | Issue: 24 | Pages: 6207

10.3390/cancers13246207 Get It

The purpose of this work was to investigate whether minibeam therapy with heavy ions might offer improvements of the therapeutic ratio for the treatment of human brain cancers. To assess neurotoxicity, we irradiated normal juvenile rats using 120 MeV lithium-7 ions at an absorbed integral dose of 20 Gy. Beams were configured either as a solid parallel circular beam or as an array of planar parallel minibeams having 300-micron width and 1-mm center-to-center spacing within a circular array. We followed animals for 6 months after treatment and utilized behavioral testing and immunohistochemical studies to investigate the resulting cognitive impairment and chronic pathologic changes. We found both solid-beam therapy and minibeam therapy to result in cognitive impairment compared with sham controls, with no apparent reduction in neurotoxicity using heavy ion minibeams instead of solid beams under the conditions of this study.
Proton minibeams—a springboard for physics, biology and clinical creativity
Dilmanian, F. Avraham, Venkatesulu, Bhanu Prasad , Sahoo, Narayan , Wu, Xiaodong , Nassimi, Jessica R., Herchko, Steven, Lu, Jiade J. , Eley, John G. , Krishnan, Sunil , Krishnan, Sunil , Dwarakanath, Bilikere Srinivasa Rao

The British Journal of Radiology | January 16, 2020 | Volume: 93 | Issue: 1107 | Pages: No page available

10.1259/bjr.20190332 Get It

Proton minibeam therapy (PMBT) is a form of spatially fractionated radiotherapy wherein broad beam radiation is replaced with segmented minibeams—either parallel, planar minibeam arrays generated by a multislit collimator or scanned pencil beams that converge laterally at depth to create a uniform dose layer at the tumor. By doing so, the spatial pattern of entrance dose is considerably modified while still maintaining tumor dose and efficacy. Recent studies using computational modeling, phantom experiments, in vitro and in vivo preclinical models, and early clinical feasibility assessments suggest that unique physical and biological attributes of PMBT can be exploited for future clinical benefit. We outline some of the guiding principle of PMBT in this concise overview of this emerging area of preclinical and clinical research inquiry.