Evidence map›Paper›PMID 42027150›Full record

ArticleMedical physics2026

A preclinical setup for spatially fractionated radiation therapy with electrons.

Edward R J F Taylor, Jia-Ling Ruan, Salomé Paillas, Iain D C Tullis, Geoff S Higgins, Kristoffer Petersson

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Article in Medical physics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Edward R J F TaylorDepartment of Oncology, University of Oxford, Oxford, UK.
Jia-Ling RuanDepartment of Oncology, University of Oxford, Oxford, UK.
Salomé PaillasDepartment of Oncology, University of Oxford, Oxford, UK.
Iain D C TullisDepartment of Oncology, University of Oxford, Oxford, UK.
Geoff S HigginsDepartment of Oncology, University of Oxford, Oxford, UK.
Kristoffer PeterssonDepartment of Oncology, University of Oxford, Oxford, UK.

Funding

Translational Studies in FLASH Particle RadiotherapyP01CA257904 · NCI · UNIVERSITY OF PENNSYLVANIA · PI Mary E. Putt · 2022 to 2026
$14.2M
Cancer Research UK - RadNet C6078/A28736Medical Research Council MR/X006611/1National Cancer Institute/NIH/DHHS 1P01CA257904NCI NIH HHS P01 CA257904
6 · The paper itself

Abstract

backgroundSpatially fractionated radiation therapy (SFRT) has therapeutic potential as a priming therapy which boosts tumor control. However, the optimal delivery and spatial fractionation parameters have not been deciphered and the mechanisms at play are not yet fully understood. PURPOSE: This paper highlights our preclinical setups for mini-grid SFRT with 6 MeV electrons delivered at conventional to ultrahigh dose rates, using a flexible collimator system. These setups let us explore relevant spatial fractionation parameters to observe their effect on tumor growth and normal tissue toxicity. Preclinical studies here may reveal the parameters of highest clinical relevance for SFRT and combination therapies.

methodsFor preclinical experiments with electron spatial fractionation, 6.5 mm thick brass collimators were made with 7- (or 19-) hole hexagonally packed ∅ 0.65-2 mm apertures, with 1.6-5 mm CTC distances. Irradiated EBT-XD Gafchromic film downstream of collimators were analyzed to obtain peak-to-valley dose ratios (PVDR), full width at half maxima (FWHM), and peak doses at various depths in solid water, and at surface when increasing the separations from collimators in air. Male and female C57BL/6 mice were injected subcutaneously with UPPL1541 bladder cancer cells in the right flank. After 10-13 days, a single dose treatment was delivered to the tumors with either ∅14 mm circular homogeneous field (10 Gy delivered at 3 kGy s

resultsSimilar PVDRs were obtained with 7- and 19-hole inserts (35 and 31 at surface, respectively). Peak widths increased with depth, and maximal peak dose rates were > 1.8 kGy s

conclusionsSpatially fractionated electron FLASH treatments with 30 Gy peak doses and 2.1 Gy valley doses provide effective tumor growth delay and prolonged tumor control akin to 10 Gy homogeneous irradiations. Here we demonstrate that combining spatial modulation, higher peak doses, and FLASH dose rates can produce favorable tumor response.

Indexed as

Dose Fractionation, RadiationElectronsAnimalsCell Line, TumorFemaleMaleMiceMice, Inbred C57BLUrinary Bladder NeoplasmselectronFLASHmini‐gridpreclinicalspatial fractionationsubcutaneous tumor

Identifiers

PMID42027150
PMCPMC13107147

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.