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Intermittent LHRH therapy in the management of castrate-resistant prostate cancer (CRPCa): results of a multi-institutional randomized prospective clinical trial.
Organ, Michael; Wood, Lori; Wilke, Derek; Skedgel, Chris; Cheng, Tina; North, Scott; Thompson, Kara; Winch, Susan; Rendon, Ricardo.
Afiliação
  • Organ M; Departments of *Urology †Medicine and Urology ‡Radiation Oncology §Atlantic Clinical Cancer Research Unit (ACCRU), Capital Health #Medicine **Urology, Centre for Clinical Research, Dalhousie University, Halifax, NS ∥Department of Medical Oncology, University of Calgary, Tom Baker Cancer Center, Calgary ¶Department of Oncology, University of Alberta, Cross Cancer Institute, Edmonton, AB, Canada.
Am J Clin Oncol ; 36(6): 601-5, 2013 Dec.
Article em En | MEDLINE | ID: mdl-22868247
BACKGROUND: Patients who develop castration-resistant prostate cancer (CRPCa) typically continue on androgen deprivation therapy (ADT). Whether these patients need to remain on ADT has not been well studied. We conducted a multicenter randomized trial to compare an intermittent versus continuous approach to ADT in CRPCa patients. Overall survival, health-related quality of life (QOL), and cost were the main endpoints. METHODS: CRPCa patients were randomized 2:1 to intermittent or continuous luteinizing hormone-releasing hormone agonists (LHRHa). Patients were followed with clinical assessments, laboratory investigations, and QOL questionnaires (EORTC QLQ-C30 or PROSQOLI) every 2 months. If the serum testosterone rose above castrate levels (1.75 nmol/L), LHRHa were reinitiated. The study was designed to close if >50% of patients needed to restart ADT in the intermittent arm. RESULTS: Thirty-one patients were followed with a median follow-up of 26.8 months-18 in the intermittent arm and 13 in the continuous. Twelve of 18 patients on the intermittent arm were reinitiated on LHRHa at a median time of 17.9 months. There was no difference in overall or cancer-specific survival between the 2 arms. There was no statistically significant difference in QOL between the 2 arms at 0 and 12 months. The total mean costs at 24 months were significantly lower in the intermittent arm ($3135 vs. $8253 Canadian dollars, P=0.0167) compared with the continuous. The main limitation of this study is the small sample size. CONCLUSIONS: We have observed that intermittent ADT in patients with CRPCa, using a testosterone of >1.75 ngmol/L as a trigger to reinitiate LHRHa, results in a substantial cost savings with no negative impact on oncologic and QOL outcomes.
Assuntos

Texto completo: 1 Coleções: 01-internacional Temas: Cuidados_paliativos / Geral / Tipos_de_cancer / Prostata Base de dados: MEDLINE Assunto principal: Hormônio Liberador de Gonadotropina / Neoplasias de Próstata Resistentes à Castração Tipo de estudo: Clinical_trials / Health_economic_evaluation / Observational_studies / Prognostic_studies Limite: Aged / Aged80 / Humans / Male / Middle aged Idioma: En Revista: Am J Clin Oncol Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Canadá

Texto completo: 1 Coleções: 01-internacional Temas: Cuidados_paliativos / Geral / Tipos_de_cancer / Prostata Base de dados: MEDLINE Assunto principal: Hormônio Liberador de Gonadotropina / Neoplasias de Próstata Resistentes à Castração Tipo de estudo: Clinical_trials / Health_economic_evaluation / Observational_studies / Prognostic_studies Limite: Aged / Aged80 / Humans / Male / Middle aged Idioma: En Revista: Am J Clin Oncol Ano de publicação: 2013 Tipo de documento: Article País de afiliação: Canadá