Predicting post-radiation genitourinary hospital admissions in patients with localised prostate cancer

医学 前列腺癌 比例危险模型 泌尿科 肾病科 泌尿生殖系统 内科学 放射治疗 前列腺 危险系数 肿瘤科 癌症 置信区间
作者
Rowan David,Mrunal Hiwase,Arman A. Kahokehr,Jason Lee,David I. Watson,John Leung,Michael O'Callaghan
出处
期刊:World Journal of Urology [Springer Science+Business Media]
标识
DOI:10.1007/s00345-022-04212-y
摘要

Abstract Purpose The risk of treatment-related toxicity is important for patients with localised prostate cancer to consider when deciding between treatment options. We developed a model to predict hospitalisation for radiation-induced genitourinary toxicity based on patient characteristics. Methods The prospective South Australian Prostate Cancer Clinical Outcomes registry was used to identify men with localised prostate cancer who underwent curative intent external beam radiotherapy (EBRT) between 1998 and 2019. Multivariable Cox proportional regression was performed. Model discrimination, calibration, internal validation and utility were assessed using C-statistics and area under ROC, calibration plots, bootstrapping, and decision curve analysis, respectively. Results There were 3,243 patients treated with EBRT included, of which 644 (20%) patients had a treated-related admission. In multivariable analysis, diabetes (HR 1.35, 95% CI 1.13–1.60, p < 0.001), smoking (HR 1.78, 95% CI 1.40–2.12, p < 0.001), and bladder outlet obstruction (BOO) without transurethral resection of prostate (TURP) (HR 7.49, 95% CI 6.18–9.08 p < 0.001) followed by BOO with TURP (HR 4.96, 95% CI 4.10–5.99 p < 0.001) were strong independent predictors of hospitalisation (censor-adjusted c-statistic = 0.80). The model was well-calibrated (AUC = 0.76). The global proportional hazards were met. In internal validation through bootstrapping, the model was reasonably discriminate at five (AUC 0.75) years after radiotherapy. Conclusions This is the first study to develop a predictive model for genitourinary toxicity requiring hospitalisation amongst men with prostate cancer treated with EBRT. Patients with localised prostate cancer and concurrent BOO may benefit from TURP before EBRT.
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