Proton arc therapy reduces the dose delivered to circulating blood compared to intensity-modulated proton therapy for head-and-neck cancer.
Document Type
Article
Publication Date
11-2026
Publication Title
Journal of applied clinical medical physics [electronic resource] / American College of Medical Physics
Abstract
BACKGROUND: Compared to intensity-modulated proton therapy (IMPT), proton arc therapy (PAT) has various dosimetric advantages. However, questions have been raised over whether the larger low-dose bath during PAT may increase radiation-induced lymphocyte killing, which is correlated with adverse clinical outcomes.
PURPOSE: The purpose of this study is to quantitatively compare radiation dose delivery to circulating blood during IMPT and PAT.
METHODS: For each of 10 head-and-neck cancer patients, one IMPT and one PAT treatment plan were created, and the hematological dose (HEDOS) blood dose model was used to simulate radiation dose delivery to circulating blood. HEDOS simulations utilized gantry angle-wise dose distributions (including for PAT) and considered gantry rotation and energy layer switching as well as irradiation times. Blood dose histograms as well as the mean dose to all simulation blood particles (D
RESULTS: For IMPT, blood dose metrics (in the form of mean over all patients ± one standard deviation) were (0.522 ± 0.204)Gy(RBE) for D
CONCLUSIONS: Compared to IMPT, proton arc therapy was associated with significantly lower radiation dose delivery to circulating blood across a variety of different metrics. Proton arc therapy for head-and-neck cancer is therefore not expected to result in higher radiation-induced killing of circulating lymphocytes compared to IMPT.
Volume
27
Issue
11
First Page
e70864
Recommended Citation
Tattenberg S, Liu P, Cong X, Hoehr C, Ding X. Proton arc therapy reduces the dose delivered to circulating blood compared to intensity-modulated proton therapy for head-and-neck cancer. J Appl Clin Med Phys. 2026 Nov;27(11):e70864. doi: 10.1002/acm2.70864. PMID: 42900560
DOI
10.1002/acm2.70864
ISSN
1526-9914
PubMed ID
42900560