It often seems difficult to decide how to manage patients with incidental prostate cancer. We analyzed our patients who underwent radical transurethral resection of prostate cancer (RTUR-PCa) and obtained satisfactory results that suggested RTUR-PCa could be an option for radical treatment against incidental cancer. Background: To evaluate the rationale for RTUR-PCa against pT1a/b cancer, we analyzed oncological and functional outcomes. Patients and Methods: Fifty-six patients with incidental prostate cancer were included and the age ranged from 66 to 91 years (mean, 76.6; median, 75.0). Preoperative prostate specific antigen (PSA) levels were between 0.70 and 44.1 ng/mL (mean, 5.90; median, 4.60). We performed 69 RTUR-PCa's by resecting and fulgurating the residual prostate tissues after previous transurethral resection of the prostate. Prostate specific antigen non-recurrence rate was calculated by Kaplan-Meier method. Results: Follow-up duration of 51 patients was mean +/- SD 64.1 +/- 21.6 months (median, 67.8 months; range, 13.8-99.8) excluding 5 patients that were lost to follow-up. Prostate specific antigen failure developed in 3 patients (5.9%). In the other 48 patients, PSA stabilized as follows: PSA <= 0.01, 24 cases; <= 0.02, 5 cases; <= 0.03, 6 cases; <= 0.04, 3 cases; <= 0.1, 7 cases; and <= 0.4, 3 cases. Prostate specific antigen nonrecurrence rates were 100% for pT2a and 91.3% for pT2b at the mean follow-up period of 64.1 months. Nonrecurrence rate grouped by D'Amico classification system were 100% in the low-risk group, 94.7% in the intermediate-risk group, and 88.2% in the high-risk group, respectively. Water intoxication did not develop and no patients required transfusion. Bladder neck contracture, which developed in 22 out of 51 patients (43.1%), was the most frequent postoperative complication. Postoperative incontinence was temporary and disappeared within 3 months in all patients. Conclusion: Satisfactory oncologic and functional results suggest that RTUR-PCa could be a promising option for radical treatment against incidental prostate cancer. (C) 2013 Elsevier Inc. All rights reserved.