Neoadjuvant Androgen Deprivation Therapy for Prostate Volume Reduction, Lower Urinary Tract Symptom Relief and Quality of Life Improvement in Men with Intermediate- to High-risk Prostate Cancer: A Randomised Non-inferiority Trial of Degarelix versus Goserelin plus Bicalutamide

被引:61
作者
Mason, M. [1 ]
Maldonado Pijoan, X. [2 ]
Steidle, C. [3 ]
Guerif, S. [4 ]
Wiegel, T. [5 ]
van der Meulen, E. [6 ]
Bergqvist, P. B. F. [6 ]
Khoo, V. [7 ,8 ]
机构
[1] Cardiff Univ, Sect Oncol & Palliat Med, Velindre Hosp, Cardiff CF14 2TL, S Glam, Wales
[2] Hosp Univ Vall dHebron, Serv Oncol Radioterap, Barcelona, Spain
[3] Northeast Indiana Res, Ft Wayne, IN USA
[4] CHU, Brachytherapy Unit, PRC, Poitiers, France
[5] Univ Hosp, Dept Radiat Oncol, Ulm, Germany
[6] Ferring Pharmaceut AS, Copenhagen, Denmark
[7] Royal Marsden NHS Fdn Trust, London, England
[8] Inst Canc Res, London SW3 6JB, England
关键词
Prostate cancer; prostate volume reduction; short-term androgen deprivation; urinary symptom management; RADIATION-THERAPY; HORMONAL-THERAPY; BRACHYTHERAPY; RADIOTHERAPY; HYPERPLASIA; CARCINOMA;
D O I
10.1016/j.clon.2012.09.010
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Aims: The treatment of intermediate- to high-risk prostate cancer with radical radiotherapy is usually in combination with neoadjuvant androgen deprivation therapy. The aim of the present trial was to investigate whether degarelix achieves comparable efficacy with that of goserelin, plus bicalutamide as neoadjuvant therapy before radiotherapy. Materials and methods: The study was a randomised, parallel-arm, active-controlled, open-label trial in 244 men with a UICC prostate cancer TNM category T2b-T4, N0, M0, Gleason score >= 7, or prostate-specific antigen >= 10 ng/ml and a total prostate volume >30 ml, who were scheduled to undergo radical radiotherapy and in whom neoadjuvant androgen deprivation therapy was indicated. Eligible patients received treatment with either monthly degarelix (240/80 mg) or goserelin (3.6 mg) for 12 weeks, the latter patients also receiving bicalutamide (50 mg) for 17 days initially. The primary efficacy measure was the mean percentage reduction in total prostate volume from baseline at week 12 measured by transrectal ultrasound. The severity and relief of lower urinary tract symptoms were assessed by the International Prostate Symptom Score questionnaire. Quality of life was assessed by the eighth question of the International Prostate Symptom Score. About 50% of the patients had moderate to severe lower urinary tract symptoms at baseline. Results: The total prostate volume decreased significantly from baseline to week 12 in both treatment groups, reaching 36.0 +/- 14.5% in degarelix-treated patients and 35.3 +/- 16.7% in goserelin-treated patients (adjusted difference: -0.3%; 95% confidence interval: -4.74; 4.14%). At the end of the therapy, more degarelix- than goserelin-treated patients reported International Prostate Symptom Score decreases of >= 3 points (37% versus 27%, P = 0.21). In addition, in patients with a baseline International Prostate Symptom Score of >= 13, the magnitude of the decrease was larger in degarelix- (n = 53) versus goserelin-treated patients (n = 17) (6.04 versus 3.41, P = 0.06). Conclusions: The efficacy of degarelix in terms of prostate shrinkage is non-inferior to that of goserelin plus bicalutamide. The added benefits of degarelix in terms of more pronounced lower urinary tract symptom relief in symptomatic patients could be the reflection of differences in the direct effects on extrapituitary receptors in the lower urinary tract [Clinicaltrials.gov ID: NCT00833248]. (C) 2012 The Royal College of Radiologists. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:190 / 196
页数:7
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