Low-dose-rate brachytherapy (LDR-BT) has become a treatment option for localized prostate cancer; however, its associated adverse events include lower urinary tract, bowel and sexual disorders, which can worsen patients' quality of life. 1 A recent review showed that late grade 3 and higher-grade complications, such as urethral stricture (1-9%), vesicourethral fistula (<0.2%), rectal ulcer (0.1-0.3%) and rectal fistula (<0.5%), are less frequent, but early post-treatment grade 1-2 complications, including lower urinary tract symptoms, such as irritative/obstructive symptoms (7-84%), acute bowel toxicity (1-7%) and erectile dysfunction (19-50%), are common. 1 To reduce lower urinary tract symptoms after LDR-BT, a-1 adrenoceptor antagonists are often used. Each a-1 antagonist has slight differences in therapeutic efficacy due to differences in the distribution of its receptor subtypes in the lower urinary tract tissues and their affinities. 2,3 To evaluate the efficacy of each a-1 antagonist after LDR-BT, Tanaka et al. designed a randomized controlled trial and assigned patients into two groups: one group received silodosin, which has a high affinity for a-1A, and other group received naftopidil, which has a high affinity for a-1D. They reported that the International Prostate Symptoms Score did not differ significantly between the two groups after LDR-BT. 2 As a subanalysis of the randomized controlled trial, Maesaka et al. investigated bowel and sexual functions in 64 patients in the silodosin group and 63 patients in the naftopidil group. 3 The results of the University of California, Los Angeles Prostate Cancer Index and Sexual Health Inventory for Men score questionnaires showed significantly better outcomes for bowel function in the silodosin group and for sexual function in the naftopidil group, with less deterioration from baseline at 1-3 months after LDR-BT. 3 This is the first report showing differences in bowel and sexual functions in the early post-LDR-BT period among different a-1 subtypes, and the results might help in choosing a drug based on patients' preoperative symptoms. Regarding sexual function, it was reported that tadarafil, a phosphodieserase-5 inhibitor, provided better Sexual Health Inventory for Men scores after LDR-BT than tamsulosin, an a-1 antagonist. 4 In actual clinical practice, to maintain quality of life after LDR-BT, it would be necessary to evaluate lower urinary tract functions (including International Prostate Symptoms Score, Overactive Bladder Symptom Score, uroflowmetry, post-void residual urine volume), sexual function including Sexual Health Inventory for Men score and bowel function before treatment, and to administer an a-1 antagonist suitable for each patient while considering the subtypes. If necessary, concomitant use of phosphodieserase-5 inhibitor and overactive bladder drugs, bowel control and dietary instructions should be considered.