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A Polygenic Risk Score for Late Bladder Toxicity Following Radiotherapy for Non-Metastatic Prostate Cancer

Farazi, M.
Yang, X.
Gehl, C. J.
Barnett, G. C.
Burnet, N. G.
Chang-Claude, J.
Parker, C. C.
Dunning, A. M.
Azria, D.
Choudhury, A.
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Abstract
BACKGROUND: Late bladder toxicity is a concern for patients receiving prostate cancer radiotherapy and negatively affects survivors. Few risk factors are known beyond the radiation dose and volume of bladder exposed. A polygenic risk score (PRS) could identify susceptible patients. METHODS: A PRS was built using genome-wide association results from the Radiogenomics Consortium (N = 3,988) and then tested in the prospective REQUITE and URWCI studies (N = 2,034). The primary outcome was time to patient-reported gross [grade ≥2, (≥G2)] hematuria, analyzed using Cox proportional hazards regression. Secondary outcomes were ≥G2 urinary retention and frequency. The PRS was externally validated for clinically diagnosed irradiation cystitis in the UK Biobank (N = 8,430). A gene-burden test evaluated rare coding variants. RESULTS: A 115-variant PRS was associated with a significantly increased risk of ≥G2 hematuria [hazard ratio (HR) per SD = 1.22; P = 0.009] as well as urinary retention (HR per SD = 1.18; P = 0.016) and frequency (HR per SD = 1.14; P = 0.036). When binarized, men in the upper decile (PRShigh) had a >2-fold increased risk of hematuria after adjusting for clinical risk factors [HR = 2.12; P = 0.002; Harrel's concordance index = 0.71 (95% confidence interval, 0.65-0.76)]. A similar effect size was seen in the UK Biobank for clinically diagnosed irradiation cystitis [odds ratio (OR) = 2.15; P = 0.026]. The burden test identified BOD1L1 as a putative novel radiosensitivity gene. CONCLUSIONS: This PRS identifies susceptible patients and could guide the selection of those needing reoptimized treatment plans that spare the bladder beyond currently recommended constraints. IMPACT: PRS-guided treatment planning in radiation oncology could lower the incidence of clinically relevant bladder toxicity and reduce the impact of this outcome on prostate cancer survivors.
Affiliation
The Medical College of Wisconsin, Milwaukee, Wisconsin. Cambridge University Hospitals NHS Foundation Trust, Cambridge, United Kingdom. The Christie NHS Foundation Trust, Manchester, United Kingdom. German Cancer Research Center (DKFZ), Heidelberg, Germany. Royal Marsden NHS Foundation Trust, Sutton, United Kingdom. Cambridge University, Cambridge, United Kingdom. Montpellier Cancer Institute ICM, Univ Montpellier, INSERM U1194 IRCM, Montpellier, France. University of Manchester, Manchester, United Kingdom. Fondazione IRCCS Istituto Nazionale dei Tumori, Milan, Italy. Maastricht University Medical Center, GROW School, Maastricht, the Netherlands. Mannheim Cancer Center, University Medical Center Mannheim, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany. University of Leicester, Leicester, United Kingdom. Ghent University/Ghent University Hospital, Ghent, Belgium. Grupo Genética en Cáncer y Enfermedades Raras, Instituto de Investigación Sanitaria de Santiago de Compostela, Santiago de Compostela, Spain. Fundación Pública Galega de Medicina Xenómica, Santiago de Compostela, Spain. Hospital Clínico Universitario de Santiago de Compostela, Servizo Galego de Saúde (SERGAS), Santiago de Compostela, Spain. Biomedical Network on Rare Diseases (CIBERER), Madrid, Spain. Albert Einstein College of Medicine, Bronx, New York. Icahn School of Medicine at Mount Sinai, New York, New York. National Tokyo Medical Center, Tokyo, Japan. Cross Cancer Institute, University of Alberta, Edmonton, Canada. University of Rochester, Rochester, New York.
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2025
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Article
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Farazi M, Yang X, Gehl CJ, Barnett GC, Burnet NG, Chang-Claude J, et al. A Polygenic Risk Score for Late Bladder Toxicity Following Radiotherapy for Non-Metastatic Prostate Cancer. Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology. 2025 May 2;34(5):795-804. PubMed PMID: 40029246. Pubmed Central PMCID: PMC12048210. Epub 2025/03/03. eng.
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