CAN FINASTERIDE REVERSE THE PROGRESS OF BENIGN PROSTATIC HYPERPLASIA - A 2-YEAR PLACEBO-CONTROLLED STUDY

被引:124
作者
ANDERSEN, JT
EKMAN, P
WOLF, H
BEISLAND, HO
JOHANSSON, JE
KONTTURI, M
LEHTONEN, T
TVETER, K
BODKER, A
VEDEL, O
NORDLING, J
POULSEN, AL
SCHOU, J
HVIDT, V
HANSEN, JB
MEYHOFF, HH
ELDRUP, J
HARTWELL, D
COLSTRUP, H
LYNGDORF, P
NIELSEN, AH
LARSEN, E
WALTER, S
LARSEN, EH
THYBO, E
MOMMSEN, S
BROK, KE
PALM, L
GENSTER, H
ANDERSEN, M
KAUPPINEN, P
RAUVALA, M
HAKKINEN, J
TAMMELA, T
TAINIO, H
HYNNINEN, O
TIITINEN, J
LEHTORANTA, K
ALAOPAS, M
PERTTILA, I
PETAS, A
RINTALA, E
SALMINEN, R
JUUSELA, H
HANSSON, E
VONWENDT, R
TUHKANEN, K
TALJA, M
NURMI, M
PUNTALA, P
机构
[1] HERLEV SYGEHUS,COPENHAGEN,DENMARK
[2] BISPEBJERG HOSP,COPENHAGEN,DENMARK
[3] HILLEROD SYGEHUS,HILLEROD,DENMARK
[4] GENTOFTE AMTS SYGEHUS,COPENHAGEN,DENMARK
[5] ESBJERG CENT SYGEHUS,ESBJERG,DENMARK
[6] NAESTVED CENT SYGEHUS,NAESTVED,DENMARK
[7] SKEJBY SYGEHUS,AARHUS,DENMARK
[8] AALBORG HOSP,AALBORG,DENMARK
[9] ODENSE HOSP,ODENSE,DENMARK
[10] ROSKILDE SYGEHUS,ROSKILDE,DENMARK
[11] SONDERBORG SYGEHUS,SONDERBORG,DENMARK
[12] UNIV OULU,CENT HOSP,SF-90220 OULU,FINLAND
[13] TAMPERE UNIV HOSP,TAMPERE,FINLAND
[14] LAHTI CITY HOSP,LAHTI,FINLAND
[15] PAIJAT HAME CENT HOSP,LAHTI,FINLAND
[16] KANTA HAME CENT HOSP,HAMEENLINNA,FINLAND
[17] UNIV HELSINKI,CENT HOSP,HELSINKI,FINLAND
[18] MALMI HOSP,HELSINKI,FINLAND
[19] LOHJA HOSP,LOHJA,FINLAND
[20] JORVI HOSP,ESPOO,FINLAND
[21] VAASA CENT HOSP,VAASA,FINLAND
[22] KUOPIO UNIV HOSP,SF-70210 KUOPIO,FINLAND
[23] TURKU UNIV,CENT HOSP,TURKU,FINLAND
[24] POHJOIS KARJALA CENT HOSP,JOENSUU,FINLAND
[25] ST JOSEFSSPITAL,REYKJAVIK,ICELAND
[26] LANDSPITALINN,REYKJAVIK,ICELAND
[27] ULLEVAL HOSP,OSLO,NORWAY
[28] AKER HOSP,OSLO,NORWAY
[29] AKERSHUS CENT HOSP,OSLO,NORWAY
[30] BUSKERUD CENT HOSP,DRAMMEN,NORWAY
[31] TELEMARK CENT HOSP,PORSGRUNN,NORWAY
[32] CENT HOSP ROGALAND,STAVANGER,NORWAY
[33] BODEN HOSP,UMEA,SWEDEN
[34] BORAS HOSP,BORAS,SWEDEN
[35] FALUN CENT HOSP,FALUN,SWEDEN
[36] OSTRA HOSP,S-41685 GOTHENBURG,SWEDEN
[37] ORNEHUFVUDSGATAN GOTHENBURG,GOTHENBURG,SWEDEN
[38] HELSINGBORG HOSP,HELSINGBORG,SWEDEN
[39] RYBOV CTY HOSP,JONKOPING,SWEDEN
[40] KARLSTAD CENT HOSP,KARLSTAD,SWEDEN
[41] MOLNDAL CTY HOSP,MOLNDAL,SWEDEN
[42] NORRKOPING HOSP,NORRKOPING,SWEDEN
[43] REG HOSP OREBRO,OREBRO,SWEDEN
[44] OSTERSUND HOSP,OSTERSUND,SWEDEN
[45] CENT HOSP SKOVDE,S-54185 SKOVDE,SWEDEN
[46] KAROLINSKA HOSP,S-10401 STOCKHOLM,SWEDEN
[47] MED CTR VALLINGBY,STOCKHOLM,SWEDEN
[48] TROLLHATTAN HOSP,TROLLHATTAN,SWEDEN
[49] UDDEVALLA CENT HOSP,UDDEVALLA,SWEDEN
[50] UNIV UPPSALA HOSP,UPPSALA,SWEDEN
关键词
D O I
10.1016/S0090-4295(99)80291-X
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Objectives. To study if placebo-induced improvement in men with symptomatic benign prostatic hyperplasia (BPH) is maintained over 2 years, and to study the efficacy and safety from intervention with finasteride 5 mg for 24 months. Methods. This was a multicenter, double-blind, placebo-controlled study involving 707 patients with moderate symptoms of BPH enrolled at 59 centers in five Scandinavian countries. Following enrollment and a 4-week single-blind placebo run-in period, patients were randomized to receive finasteride 5 mg once daily or placebo for 24 months. Urinary symptoms, urinary flow rate, prostate volume, postvoiding residual urinary volume, and serum concentrations of prostate-specific antigen together with laboratory safety parameters were measured at entry and at months 12 and 24. Interim physical and laboratory examinations were performed when indicated clinically. Results. In finasteride-treated patients the total symptom score improved throughout the study, with a significant difference between the two groups at 24 months (P less than or equal to 0.01), whereas in placebo-treated patients, there was an initial improvement in the symptom score but no change from baseline at 24 months. The maximum urinary flow rate decreased in the placebo group, but improved in the finasteride group, resulting in a between-group difference of 1.8 mL/s at 24 months (P less than or equal to 0.01). The mean change in prostate volume was +12% in the placebo group versus -19% in the finasteride-treated group (P < 0.01). Finasteride was generally well tolerated throughout the 2-year study period. Conclusions. The efficacy of therapy with finasteride 5 mg in improving both symptoms and maximum urinary flow rate and reducing prostate volume has been shown to be maintained during 24 months while patients receiving placebo experienced a return to baseline or deterioration of these parameters during the study. These results demonstrate that finasteride can reverse the natural progression of BPH.
引用
收藏
页码:631 / 637
页数:7
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