Intermediate rectal dose is associated with late toxicity after prostate SBRT: a dose–volume histogram principal component analysis

PURPOSE: To evaluate whether principal component analysis (PCA) of rectal and bladder dose-volume histograms (DVHs) identifies dose regions associated with late toxicity after prostate stereotactic body radiotherapy (SBRT). METHODS/PATIENTS: This retrospective single-institution study included 106 patients with linked clinical and dosimetric data after prostate SBRT to 36.25 Gy in five fractions. PCA was applied separately to whole-organ and wall-based rectal and bladder DVHs. Associations with late grade ≥ 2 gastrointestinal (GI) and genitourinary (GU) toxicity at 12 months were explored using Spearman correlation, ROC analysis and deliberately limited logistic regression. Toxicity was extracted retrospectively from institutional follow-up records scored according to CTCAE v5.0. RESULTS: Among 84 patients with 12-month follow-up in the DVH-linked dosimetric cohort, grade ≥ 2 toxicity was uncommon, with 3 GI events (3.6%) and 2 GU events (2.4%). Intermediate-dose rectal metrics showed the strongest exploratory signal for late GI toxicity, particularly rectal V18.1 Gy (AUC 0.868, 95% CI 0.740-0.997) and V29 Gy (AUC 0.827). These estimates are based on very few events and should not be interpreted as validated predictive performance or as evidence of a new planning threshold. No bladder or bladder-wall metric showed clinically meaningful discrimination for GU toxicity. CONCLUSIONS: Intermediate whole-rectum dose was associated with late GI toxicity in this low-event SBRT cohort, but the findings are exploratory and require validation. No isolated dosimetric predictor of late GU toxicity was identified.

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Publication Details

Journal
Clinical & Translational Oncology
Published
2026-08-03
DOI
https://doi.org/10.1007/s12094-026-04522-2
Primary Topic
Prostate Cancer Diagnosis and Treatment
Type
article
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article

Intermediate rectal dose is associated with late toxicity after prostate SBRT: a dose–volume histogram principal component analysis

Ana Illescas Vacas, Paula Vicente Ruiz, Amadeo Wals-Zurita, J. Saavedra Bejarano et al.
Clinical & Translational Oncology
Prostate Cancer Diagnosis and Treatment
article

Intermediate rectal dose is associated with late toxicity after prostate SBRT: a dose–volume histogram principal component analysis

Ana Illescas Vacas, Paula Vicente Ruiz, Amadeo Wals-Zurita, J. Saavedra Bejarano, María Rubio Jiménez, Antonio Ureña, Mónica Ortiz Seidel, Francisco Carrasco Peña, Héctor Miras del Río
article en

Abstract

PURPOSE: To evaluate whether principal component analysis (PCA) of rectal and bladder dose-volume histograms (DVHs) identifies dose regions associated with late toxicity after prostate stereotactic body radiotherapy (SBRT). METHODS/PATIENTS: This retrospective single-institution study included 106 patients with linked clinical and dosimetric data after prostate SBRT to 36.25 Gy in five fractions. PCA was applied separately to whole-organ and wall-based rectal and bladder DVHs. Associations with late grade ≥ 2 gastrointestinal (GI) and genitourinary (GU) toxicity at 12 months were explored using Spearman correlation, ROC analysis and deliberately limited logistic regression. Toxicity was extracted retrospectively from institutional follow-up records scored according to CTCAE v5.0. RESULTS: Among 84 patients with 12-month follow-up in the DVH-linked dosimetric cohort, grade ≥ 2 toxicity was uncommon, with 3 GI events (3.6%) and 2 GU events (2.4%). Intermediate-dose rectal metrics showed the strongest exploratory signal for late GI toxicity, particularly rectal V18.1 Gy (AUC 0.868, 95% CI 0.740-0.997) and V29 Gy (AUC 0.827). These estimates are based on very few events and should not be interpreted as validated predictive performance or as evidence of a new planning threshold. No bladder or bladder-wall metric showed clinically meaningful discrimination for GU toxicity. CONCLUSIONS: Intermediate whole-rectum dose was associated with late GI toxicity in this low-event SBRT cohort, but the findings are exploratory and require validation. No isolated dosimetric predictor of late GU toxicity was identified.

Clinical & Translational Oncology
Hospital Universitario Virgen Macarena (ES)
Peace, Justice and strong institutions
Openalex Percentile: Top 10%
Prostate Cancer Diagnosis and Treatment
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