A prospective, randomized, open-label, parallel trial comparing the efficacy of α-blocker or 5α-reductase inhibitor withdrawal to continued combination therapy on the maintenance of lower urinary tract symptoms in men with benign prostatic hyperplasia

被引:1
|
作者
Lee, Kwang Suk [1 ]
Yoo, Jeong Woo [1 ]
Kim, Dae Ho [1 ]
Jeon, Soyoung [2 ]
Yang, Juyeon [2 ]
Chung, Byung Ha [1 ]
Koo, Kyo Chul [1 ,3 ]
机构
[1] Yonsei Univ, Coll Med, Dept Urol, Seoul, South Korea
[2] Yonsei Univ, Coll Med, Med Res Ctr, Biostat Collaborat Unit, Seoul, South Korea
[3] Yonsei Univ, Coll Med, Dept Urol, 211 Eonju Ro, Seoul 135720, South Korea
来源
PROSTATE | 2024年 / 84卷 / 04期
关键词
5-alpha reductase inhibitors; adrenergic alpha-1 receptor antagonists; lower urinary tract symptoms; prostatic hyperplasia; FINASTERIDE; DUTASTERIDE; ENLARGEMENT; TAMSULOSIN; DOXAZOSIN;
D O I
10.1002/pros.24663
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: It is uncertain how long combination therapy should be continued in patients with benign prostatic hyperplasia (BPH) and lower urinary tract symptoms (LUTS). We investigated the withdrawal effects of alpha 1-adrenergic receptor blocker (AB) or 5 alpha-reductase inhibitor (5ARI) following successful combination therapy.Methods: This prospective, randomized, open-label, parallel trial enrolled 222 patients with BPH/LUTS who showed at least a seven-point improvement in International Prostate Symptom Score-total (IPSS-T) and a >= 20% reduction in prostate volume (PV) following the initiation of combination therapy. Patients were randomized in a 1:1:1 ratio into continued-combination, AB-withdrawal, and 5ARI-withdrawal groups. IPSS, overactive bladder symptom score, EuroQol-five-dimensional questionnaire (EQ-5D-5L), EuroQol-visual analog scale (EQ-VAS), prostate volume (PV), maximal flow rate, postvoid residual urine (PVR), and prostate-specific antigen level were assessed every 6 months for 24 months. The predictors of IPSS-T deterioration were evaluated.Results: At Month 24, IPSS-T deterioration (>= 2 point) was observed in 20/72 (27.8%) and 19/72 (26.4%) patients in the AB- and 5ARI-withdrawal groups, respectively. Among them, 4/72 (5.6%) and 4/70 (5.7%) patients required readdition of the withdrawn drug (p = 0.868). In the continued combination group, EQ-VAS improved at Month 24 compared to baseline (p = 0.028). At Month 24, the AB-withdrawal group showed improvements in EQ-5D-5L, EQ-VAS, and PVR (all p < 0.005), while the 5ARI-withdrawal group showed improvement in IPSS-S (p = 0.011). Diabetes mellitus was associated with IPSS-T deterioration at Month 24 (p = 0.020).Conclusions: In patients with BPH/LUTS who are reluctant to continue combination therapy, AB or 5ARI withdrawal may be offered in men with improvement in IPSS-T by at least seven points and reduction in PV by at least 20%.
引用
收藏
页码:403 / 413
页数:11
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