Degarelix versus Goserelin ( plus Antiandrogen Flare Protection) in the Relief of Lower Urinary Tract Symptoms Secondary to Prostate Cancer: Results from a Phase IIIb Study (NCT00831233)

被引:43
作者
Anderson, John [1 ]
Al-Ali, Ghandi [2 ]
Wirth, Manfred [3 ]
Benejam Gual, Joan [4 ]
Gomez Veiga, Francisco [5 ]
Colli, Enrico [6 ]
van der Meulen, Egbert [7 ]
Persson, Bo-Eric [8 ]
机构
[1] Royal Hallamshire Hosp, Dept Urol, Sheffield S10 2JF, S Yorkshire, England
[2] VITURO Gesell Klin Studien, Urol Gesundheitszentrum, Leipzig, Germany
[3] Tech Univ Dresden, Univ Hosp Carl Gustav Carus Dresden, Dept Urol, D-01062 Dresden, Germany
[4] Hosp Manacor, Dept Urol, Manacor, Spain
[5] Univ A Coruna, Complexo Hosp, Dept Urol, La Coruna, Spain
[6] Ferring Pharmaceut, Global Clin Res & Dev, Copenhagen, Denmark
[7] Ferring Pharmaceut, Stat, Copenhagen, Denmark
[8] Ferring Pharmaceut, Urol Oncol, St Prex, Switzerland
关键词
Degarelix; Goserelin; Lower urinary tract symptoms; Prostate cancer; STIMULATING-HORMONE RECEPTOR; QUALITY-OF-LIFE; ANTAGONIST CETRORELIX; RADICAL PROSTATECTOMY; RADIATION-THERAPY; GNRH RECEPTOR; OPEN-LABEL; EXPRESSION; MEN; BRACHYTHERAPY;
D O I
10.1159/000345423
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
Introduction: No studies to date have assessed the efficacy/tolerability of degarelix in the relief of lower urinary tract symptoms (LUTS) secondary to prostate cancer (PrCa). Methods: Patients were randomised to degarelix 240/80 mg or goserelin 3.6 mg + bicalutamide flare protection (G+B); both treatments were administered for 3 months. The primary endpoint was change in International Prostate Symptom Score (IPSS) at week 12 compared with baseline. Results: This study was stopped early due to recruitment difficulties. 40 patients received treatment (degarelix n = 27; G+B n = 13); most had locally advanced disease and were highly symptomatic. Degarelix was non-inferior to G+B in reducing IPSS at week 12 in the full analysis set (p = 0.20); the significantly larger IPSS reduction in the per-protocol analysis (p = 0.04) was suggestive of superior reductions with degarelix. Significantly more degarelix patients had improved quality of life (IPSS question) at week 12 (85 vs. 46%; p = 0.01). Mean prostate size reductions at week 12 were 42 versus 25% for patients receiving degarelix versus G+B, respectively (p = 0.04; post hoc analysis). Most adverse events were mild/moderate; more degarelix patients experienced injection site reactions whereas more G+B patients had urinary tract infections/cystitis. Conclusion: In 40 men with predominantly locally advanced PrCa and highly symptomatic LUTS, degarelix was at least non-inferior to G+B in reducing IPSS at week 12. Copyright (C) 2012 S. Karger AG, Basel
引用
收藏
页码:321 / 328
页数:8
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