ArticleJournal of applied clinical medical physics2025
The effect of interfractional variation on delivered dose with ultrahypofractionated pencil beam scanning proton therapy for localized prostate cancer.
Article in Journal of applied clinical medical physics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
- The effect of interfractional variation on delivered dose with ultrahypofractionated pencil beam scanning proton therapy for localized prostate cancer.Journal of applied clinical medical physics · 2025Article
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Authors and funding
10 authors.
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No grant is acknowledged in the PubMed record.
Abstract
PURPOSE/
objectivesProton stereotactic body radiotherapy (SBRT) using the pencil beam scanning (PBS) technique is increasingly used for localized prostate cancer (PCa) due to its potential for superior normal tissue sparing. However, interfractional anatomical variations pose challenges for accurate dose delivery, especially in ultrahypofractionation. This study investigates the dosimetric impact of these variations in PCa patients treated with PBS-SBRT.
methodsForty-two low- or intermediate-risk PCa patients treated with PBS-SBRT (36.25/ 40 Gy in 5 fractions) were included. Delivered doses were calculated by applying the initial plans to HU and artifact-corrected pre-treatment cone-beam computed tomography (CBCT) images. Dosimetric parameters were evaluated per fraction. Key anatomical features included clinical target volume (CTV) shifts in the superior-inferior (SI) and anterior-posterior (AP) directions, and volume changes in the bladder and rectum. These features were used to predict deviations in CTV D
resultsCTV AP shifts and bladder/rectum volume changes were significant predictors of dosimetric deviations. Univariate analyses indicated that bladder volume increases > 109.80 cc were strongly associated with deviations in CTV D
conclusionMultivariate models incorporating bladder volume changes and CTV shifts accurately predict dosimetric deviations in PBS-SBRT. These findings highlight the need for adaptive strategies during PBS-SBRT to mitigate the impact of interfractional variations, optimize dose delivery precision, and reduce toxicity in high-risk patients.
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