Evidence map›Paper›PMID 42634850›Full record

ArticleMedical physics2026

Multi-fidelity Monte Carlo fusion for BNCT dose calculation using a dual-branch network.

Leiming Li, Xin Hong, Yongquan Wang, Gan Huang, Zhiqiang Wu, Yingjie Xiao, Hiroki Tanaka, Hiroshi Watabe

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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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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Leiming LiGraduate School of Biomedical Engineering, Tohoku University, Sendai, Japan.ORCID https://orcid.org/0009-0007-2380-3972
Xin HongGraduate School of Biomedical Engineering, Tohoku University, Sendai, Japan.
Yongquan WangSchool of Nuclear Science and Technology, Lanzhou University, Lanzhou, China.
Gan HuangSchool of Nuclear Science and Technology, Lanzhou University, Lanzhou, China.
Zhiqiang WuGraduate School of Biomedical Engineering, Tohoku University, Sendai, Japan.
Yingjie XiaoGraduate School of Biomedical Engineering, Tohoku University, Sendai, Japan.
Hiroki TanakaDivision of Particle Radiation Medical Physics Institute for Integrated Radiation and Nuclear Science, Kyoto University, Osaka, Japan.
Hiroshi WatabeGraduate School of Biomedical Engineering, Tohoku University, Sendai, Japan.

Funding

China Scholarship CouncilJapan Society for the Promotion of Science (JSPS) KAKENHI 23H03774Japan Society for the Promotion of Science (JSPS) KAKENHI 23K07087Japan Society for the Promotion of Science (JSPS) KAKENHI 25K11003
6 · The paper itself

Abstract

backgroundBoron neutron capture therapy (BNCT) is a binary radiotherapy that selectively kills tumor cells. Its clinical implementation relies on Monte Carlo (MC)-based treatment planning systems, which are time-consuming and limit clinical workflow efficiency. PURPOSE: To address this limitation, we propose a Multi-Fidelity MC-based Dual-Branch Network (MFMC-DBN) that leverages complementary information from low- and high-fidelity MC simulations through dual-branch feature fusion, enabling accurate and efficient BNCT dose calculation.

methodsThe model was trained, validated, and tested using clinical data from 112 glioblastoma patients. Low-statistics coarse and fine mesh MC dose distributions (6.5×10

resultsMFMC-DBN outperformed both the NN and MC denoising methods across evaluated metrics. It achieved a mean absolute percentage error (MAPE) of 1.98% in the gross tumor volume (GTV). Organ-specific MAPEs ranged from 1.1% to 3.9%, with a maximum mean absolute error (MAE) of0.28 Gy (RBE). Gamma analysis further showed high spatial agreement, with passing rates of 99.8% within the patient contour and 99.3% in the GTV under the 3%/3 mm criterion. The proposed method maintained high dosimetric accuracy while substantially accelerating BNCT dose calculation.

conclusionsMFMC-DBN effectively integrates multi-fidelity MC information through a dual-branch attention mechanism, enabling rapid and accurate 3D BNCT dose prediction. By significantly reducing computation time compared with full MC simulations while preserving dosimetric fidelity, these results support the feasibility of the proposed framework for accelerated BNCT dose calculation under a fixed beam configuration.

Indexed as

Boron Neutron Capture TherapyMonte Carlo MethodNeural Networks, ComputerRadiation DosageRadiotherapy Planning, Computer-AssistedGlioblastomaHumansRadiotherapy Dosageboron neutron capture therapydeep learningdose calculationMonte Carlo simulation

Identifiers

PMID42634850
PMCPMC13501215

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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.