Evidence map›Paper›PMID 41593752›Full record

ArticleBreast cancer research : BCR2026

Toxicity profiles of proton and photon radiotherapy in postoperative breast cancer: a 10-year real-world cohort study.

Chi-Chang Yu, Ching-Chuan Hsieh, Yi-Ting Huang, Chia-Hui Chu, Wen-Cheng Chen, Miao-Fen Chen

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Article in Breast cancer research : BCR, 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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5 · Who and what money

Authors and funding

6 authors.

Chi-Chang YuDepartment of General Surgery, Chang Gung Memorial Hospital at Linko, Taoyuan, Taiwan.
Ching-Chuan HsiehDepartment of General Surgery, Chang Gung Memorial Hospital at Chiayi, Chiayi, Taiwan.
Yi-Ting HuangDepartment of Radiation Oncology, Chang Gung Memorial Hospital at Linko, Taoyuan, Taiwan.
Chia-Hui ChuDepartment of General Surgery, Chang Gung Memorial Hospital at Linko, Taoyuan, Taiwan.
Wen-Cheng ChenDepartment of Radiation Oncology, Chang Gung Memorial Hospital at Chiayi, Chiayi, Taiwan.
Miao-Fen ChenDepartment of Radiation Oncology, Chang Gung Memorial Hospital at Linko, Taoyuan, Taiwan. miaofen@adm.cgmh.org.tw.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundProton therapy, with its superior dose distribution, has emerged as a promising radiotherapy (RT) technique. This study evaluates the clinical benefits of proton therapy in reducing treatment-related toxicities in breast cancer patients undergoing radiotherapy.

methodsA retrospective analysis was performed using the Chang Gung Research Database, identifying 8189 breast cancer patients treated with adjuvant radiotherapy from 2012 to 2022. Patients received either intensity-modulated proton therapy (IMPT, n = 501) or photon-based IMRT/VMAT (n = 7688). Propensity score weighting was applied to adjust for baseline differences. The clinical outcomes photon and proton therapy were investigated, with a particular focus on radiation-induced toxicities including dermatitis, pulmonary changes, and cardiac events. In addition, N-terminal pro-brain natriuretic peptide (NT-proBNP), a biomarker of cardiac stress, was prospectively assessed in a subset of patients to assess subclinical cardiac injury between 2023 and 2024.

resultsCompared with photon therapy, proton therapy significantly reduced the incidence of radiographic pulmonary changes and subclinical cardiac biomarker elevations, while maintaining comparable loco-regional control and overall survival. Proton therapy significantly reduced the incidence of radiographic pulmonary changes (5.8% vs. 10.0%, p = 0.02; HR: 0.64, 95% CI 0.44–0.93) and grade 2 radiation dermatitis (13.4% vs. 20.9%, p < 0.001), though grade ≥ 1 skin toxicity was more common with IMPT (82% vs. 57.1%). Among left-sided patients, photon RT resulted in significantly greater NT-proBNP elevation post-treatment compared to proton therapy (mean ratio: 1.16 vs. 0.95, p = 0.0099), suggesting more subclinical cardiac stress. However, no significant difference in clinically evident cardiac events was noted between the groups during the follow-up period.

conclusionsProton therapy is associated with reduced radiation-induced pulmonary toxicity and moderate dermatitis, while achieving comparable oncologic outcomes to photon therapy. The lower NT-proBNP elevation suggests potential cardiac sparing, although longer follow-up is needed to confirm clinically meaningful cardiac benefits. These findings highlight the potential role of proton therapy in mitigating treatment-related toxicities in breast cancer patients at elevated risk for cardiopulmonary complications.

Indexed as

Breast NeoplasmsPhotonsProton TherapyRadiation InjuriesAdultAgedFemaleHumansMiddle AgedNatriuretic Peptide, BrainPeptide FragmentsRadiotherapy, AdjuvantRadiotherapy, Intensity-ModulatedRetrospective StudiesNatriuretic Peptide, BrainPeptide Fragmentspro-brain natriuretic peptide (1-76)Breast cancerProton therapyRT-induced toxicity

Identifiers

PMID41593752
PMCPMC12917995

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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.