Development of castration resistance in prostate cancer patients treated with luteinizing hormone-releasing hormone analogues (LHRHa): results of the ANARESISTANCE study.


Por: Angulo JC, Ciria Santos JP, Gómez-Caamaño A, Poza de Celis R, González Sala JL, García Garzón JM, Galán-Llopis JA, Pérez Sampietro M, Perrot V and Planas Morin J

Publicada: 1 oct 2022 Ahead of Print: 4 sep 2022
Resumen:
PURPOSE: Evaluate the percentage of patients with prostate cancer treated with luteinizing hormone-releasing hormone analogues (LHRHa) that develop castration resistance after a follow-up period of 3 years. The secondary objective is to evaluate the variables potentially related to the progression to castration resistant prostate cancer (CRPC). METHODS: A post-authorization, nation-wide, multicenter, prospective, observational, and longitudinal study that included 416 patients treated with LHRHa between 2012 and 2017 is presented. Patients were followed for 3 years or until development of CRPC, thus completing a per-protocol population of 350 patients. A Cox regression analysis was carried out to evaluate factors involved in progression to CRPC. RESULTS: After 3 years of treatment with LHRHa 18.2% of patients developed CRPC. In contrast, in the subgroup analysis, 39.6% of the metastatic patients developed CRPC, compared with 8.8% of the non-metastatic patients. The patients with the highest risk of developing CRPC were those with a nadir prostate-specific antigen (PSA) > 2 ng/ml (HR 21.6; 95% CI 11.7-39.8; p < 0.001) and those receiving concomitant medication, most commonly bicalutamide (HR 1.8; 95% CI 1-3.1, p = 0.0431). CONCLUSIONS: The proportion of metastatic patients developing CRPC after 3 years of treatment with LHRHa is consistent with what has been previously described in the literature. In addition, this study provides new findings on CRPC in non-metastatic patients. Concomitant medication and nadir PSA are statistically significant predictive factors for the time to diagnosis of CRPC, the nadir PSA being the strongest predictor.

Filiaciones:
Angulo JC:
 Clinical Department, Universidad Europea de Madrid

 Hospital Universitario de Getafe, Madrid, Spain.

Ciria Santos JP:
 Radiation Oncology Service, Hospital Universitario Donostia, Donostia, Spain

Gómez-Caamaño A:
 Department of Radiation Oncology, Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, Spain

Poza de Celis R:
 Department of Radiation Oncology, Hospital Universitario Araba, Gasteiz, Spain

González Sala JL:
 Urology Service, Corporació Sanitària Parc Taulí, Sabadell, Spain

García Garzón JM:
 Urology Service, Hospital General de Llerena, Llerena, Spain

:
 Urology Service, Hospital General Universitario de Alicante, Alicante, Spain

Pérez Sampietro M:
 Ipsen Pharma, S.A.U, Barcelona, Spain

Perrot V:
 Ipsen Pharma, S.A.U, Barcelona, Spain

Planas Morin J:
 Urology Service, Hospital Universitario Vall d'Hebrón, Barcelona, Spain
ISSN: 07244983





WORLD JOURNAL OF UROLOGY
Editorial
SPRINGER, 233 SPRING ST, NEW YORK, NY 10013 USA, Alemania
Tipo de documento: Article
Volumen: 40 Número: 10
Páginas: 2459-2466
WOS Id: 000849672600001
ID de PubMed: 36057895
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