Evidence map›Paper›PMID 42613851›Full record

ArticleMedical physics2026

Impact of millimeter-scale target motion on the precision of spatially fractionated radiation therapy using proton minibeams.

Oxana Actis, Cristian Fernandez-Palomo, Verdiana Trappetti, Michele Togno, Paolo Pellicioli, Dominic Leiser, David Meer, Valentin Djonov

Abstract read
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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

8 authors.

Oxana ActisCenter for Proton Therapy, Paul Scherrer Institute, Villigen PSI, Aargau, Switzerland.
Cristian Fernandez-PalomoInstitute of Anatomy, University of Bern, Bern, Switzerland.
Verdiana TrappettiInstitute of Anatomy, University of Bern, Bern, Switzerland.
Michele TognoCenter for Proton Therapy, Paul Scherrer Institute, Villigen PSI, Aargau, Switzerland.
Paolo PellicioliInstitute of Anatomy, University of Bern, Bern, Switzerland.
Dominic LeiserCenter for Proton Therapy, Paul Scherrer Institute, Villigen PSI, Aargau, Switzerland.
David MeerCenter for Proton Therapy, Paul Scherrer Institute, Villigen PSI, Aargau, Switzerland.
Valentin DjonovInstitute of Anatomy, University of Bern, Bern, Switzerland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWhile pencil beam scanning (PBS) with motion mitigation such as re-scanning, breath hold, or gating is well established for treating moving targets in clinical practice, the precision for Spatially Fractionated Radiation Therapy (SFRT) using proton minibeams introduces presents a unique challenge. The sub-millimeter precision required for SFRT cannot be achieved with typical PBS spot sizes (millimeters), necessitating multi-slit beam collimation, which reduces the dose rate and reintroduces motion as a critical issue. In this study, we report on our experience with minibeam irradiations of chorioallantoic membranes (CAM) of chick embryos and discuss potential solutions to the motion problem.

methodsThe first experiment was conducted at a PBS gantry using 130 MeV protons and a 6 cm thick copper multi-slit collimator with 0.3 mm wide slits and 1 mm spacing. To achieve a target peak dose of 30 Gy, CAM samples were irradiated with more than 10 re-scans. Due to a 91% beam loss in the collimator, the total irradiation time extended to two min.

resultsPost-irradiation analysis using gafchromic film revealed smearing of the minibeam profiles, while biological tissue analysis uncovered unexpected and disrupted dose effects, likely caused by irregular CAM movement during irradiation. A subsequent experiment, incorporating additional setup optimizations such as reduced air gap and increased dose rate, shortened the irradiation time to below one min. This led to sharper dose profiles with negligible variation in valley dose and peak width, although a reduction in peak dose of 8%-13% was still observed. This variation is considered acceptable for our biological experiments.

conclusionsFor clinical applications, minibeam re-scanning is likely to be feasible only under ultra-high dose rate conditions (e.g., those required to induce the FLASH effect), where sufficiently short irradiation times minimize motion-induced dose degradation.

Indexed as

Dose Fractionation, RadiationProton TherapyAnimalsChick EmbryoChorioallantoic MembraneMovementbeam deliveryminibeamsproton therapy

Identifiers

PMID42613851
PMCPMC13486916

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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.