TY - JOUR
T1 - Development of nomogram to predict acute urinary retention or surgical intervention, with or without dutasteride therapy, in men with benign prostatic hyperplasia
AU - Slawin, Kevin M.
AU - Kattan, Michael W.
AU - Roehrborn, Claus
AU - Wilson, Timothy
N1 - Funding Information:
K. M. Slavin is a co-founder of Oncovance and is a study investigator partially funded by GlaxoSmithKline. M. W. Kattan is a co-founder of Oncovance. C. G. Roehrborn is a study investigator partially funded by, and is a paid consultant to, GlaxoSmithKline.
PY - 2006/1
Y1 - 2006/1
N2 - Objectives. To develop a prediction model, or nomogram, that would predict the probability that a man with benign prostatic hyperplasia would experience acute urinary retention (AUR) or require surgical intervention (SI) within 2 years, with or without dutasteride therapy. Methods. We modeled 4294 men treated in the Phase III dutasteride benign prostatic hyperplasia trials. These men were characterized at baseline by a number of parameters, including the American Urological Association Symptom Index, Benign Prostatic Hyperplasia Impact Index questionnaire, prior use of selective alpha1-blockers, prostate volume, prostate-specific antigen level, and maximal flow rate. Cox proportional hazards regression analysis was used to relate these baseline variables to their future probability of AUR/SI within 2 years. The nomogram was internally validated with bootstrapping to assess its discrimination and calibration. Discrimination was quantified as the concordance index. Results. The nomogram appeared to be accurately calibrated and discriminating (concordance index 0.71, P <0.001). Conclusions. We constructed a nomogram for predicting the probability that a man would experience AUR or require SI within 2 years of benign prostatic hyperplasia diagnosis. At 24 months of follow-up, 7.4% of placebo patients and 3.7% of dutasteride patients had experienced AUR and/or SI, representing a 50% relative risk reduction and a 3.7% absolute risk reduction. For the greatest risk patient randomized to the Phase III dutasteride trial, the nomogram predicted a maximal risk of 27%, significantly greater than the median risk of the placebo-treated patients.
AB - Objectives. To develop a prediction model, or nomogram, that would predict the probability that a man with benign prostatic hyperplasia would experience acute urinary retention (AUR) or require surgical intervention (SI) within 2 years, with or without dutasteride therapy. Methods. We modeled 4294 men treated in the Phase III dutasteride benign prostatic hyperplasia trials. These men were characterized at baseline by a number of parameters, including the American Urological Association Symptom Index, Benign Prostatic Hyperplasia Impact Index questionnaire, prior use of selective alpha1-blockers, prostate volume, prostate-specific antigen level, and maximal flow rate. Cox proportional hazards regression analysis was used to relate these baseline variables to their future probability of AUR/SI within 2 years. The nomogram was internally validated with bootstrapping to assess its discrimination and calibration. Discrimination was quantified as the concordance index. Results. The nomogram appeared to be accurately calibrated and discriminating (concordance index 0.71, P <0.001). Conclusions. We constructed a nomogram for predicting the probability that a man would experience AUR or require SI within 2 years of benign prostatic hyperplasia diagnosis. At 24 months of follow-up, 7.4% of placebo patients and 3.7% of dutasteride patients had experienced AUR and/or SI, representing a 50% relative risk reduction and a 3.7% absolute risk reduction. For the greatest risk patient randomized to the Phase III dutasteride trial, the nomogram predicted a maximal risk of 27%, significantly greater than the median risk of the placebo-treated patients.
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U2 - 10.1016/j.urology.2005.07.013
DO - 10.1016/j.urology.2005.07.013
M3 - Article
C2 - 16413338
AN - SCOPUS:30344437996
SN - 0090-4295
VL - 67
SP - 84
EP - 88
JO - Urology
JF - Urology
IS - 1
ER -