Evidence map›Paper›PMID 42891476›Full record

ArticleJournal of medical physics

Deep Learning-based Volumetric Modulated Arc Therapy Dose Prediction with Uncertainty Quantification for Left- and Right-sided Breast Cancer: A Single-institution Feasibility Study.

Thanakorn Sukha, Chanon Puttanawarut, Nat Sirirutbunkajorn, Pimolpun Changkaew, Nauljun Stansook, Suphalak Khachonkham

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Article in Journal of medical physics. 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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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Thanakorn Sukha *Department of Diagnostic and Therapeutic Radiology, Master of Science Program in Medical Physics, Faculty of Medicine, Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Chanon Puttanawarut *Department of Clinical Epidemiology and Biostatistics, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Nat SirirutbunkajornDepartment of Diagnostic and Therapeutic Radiology, Division of Radiation and Oncology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Pimolpun ChangkaewDepartment of Diagnostic and Therapeutic Radiology, Division of Radiation and Oncology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Nauljun StansookDepartment of Diagnostic and Therapeutic Radiology, Division of Radiation and Oncology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.
Suphalak KhachonkhamDepartment of Diagnostic and Therapeutic Radiology, Division of Radiation and Oncology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, Thailand.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Volumetric-modulated arc therapy (VMAT) enables precise tumor targeting while minimizing dose to organs at risk but requires time-consuming planning with quality variability. Most deep learning (DL) dose prediction studies focus on left-sided breast cancer, with limited exploration of right-sided cases or integrated uncertainty quantification. This study investigates the feasibility of a DL model for VMAT dose prediction in both left-and right-sided breast cancer, incorporating Monte Carlo dropout (MCD)-based uncertainty quantification within a single-institution dataset. Methods: A total of 68 clinically accepted breast cancer VMAT treatment plans (41 left-sided, 27 right-sided) were collected. A three-dimensional U-Net architecture was implemented. Two models with dropout rates of 0.25 (M0.25) and 0.50 (M0.50) were developed. MCD was applied for uncertainty quantification. Performance was evaluated using mean absolute error (MAE), gamma passing rate (GPR), and isodose Dice similarity coefficients. Results: The overall body MAE was 1.7 ± 0.11 Gy (M0.25) and 1.93 ± 0.11 Gy (M0.50). For the planning target volume (PTV) of 42.56 Gy, MAE was 0.93 ± 0.17 Gy (M0.25) and 0.88 ± 0.15 Gy (M0.50). The heart showed the lowest errors (M0.25: 0.87 ± 0.34 Gy; M0.50: 1.06 ± 0.38 Gy), while contralateral lung exhibited higher uncertainties. GPR at 3%/3 mm reached 85.5% for both models, with no significant difference between left- and right-sided cases. Uncertainty maps correlated with prediction errors (Pearson correlation =0.59) and identified regions with atypical anatomies. Conclusions: The proposed model supports the feasibility of VMAT dose prediction for both left-and right-sided breast cancer, while the uncertainty maps provide additional confidence information to assist clinical interpretation and decision-making. Uncertainty maps correlated with prediction error and flagged atypical cases. External validation with a larger, multi-institutional dataset is required before clinical implementation can be considered.

Indexed as

Breast cancerdeep learningdose predictionMonte Carlo dropoutuncertainty quantificationvolumetric-modulated arc therapy

Identifiers

PMID42891476
PMCPMC13675035

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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.