Apalutamide, darolutamide and enzalutamide in nonmetastatic castration-resistant prostate cancer: a meta-analysis

Author:

Roumiguié Mathieu1ORCID,Paoletti Xavier23ORCID,Neuzillet Yann4ORCID,Mathieu Romain5ORCID,Vincendeau Sebastien6ORCID,Kleinclauss François7ORCID,Mejean Arnaud8ORCID,Guy Laurent9ORCID,Timsit Marc Olivier10ORCID,Lebret Thierry4ORCID

Affiliation:

1. Department of Urology, CHU-Institut Universitaire du Cancer de Toulouse, Toulouse, France

2. Department of Public health, University of Versailles, Saint-Quentin, France

3. Institut Curie, INSERM U900, Biostatistics for Personalized Medicine, Saint-Cloud, France

4. Department of Urology, Hôpital Foch, University of Paris-Saclay, Versailles Saint-Quentin-en-Yvelines, Suresnes, France

5. Department of Urology, Univ rennes, CHU Rennes, Inserm, EHESP, Irset – UMR_S 1085, F 35000 Rennes, France

6. Department of Urology, Centre Hospitalier Privé Saint Grégoire, Saint-Grégoire, France

7. Department of Urology, Andrology & Kidney Transplantation, University of Franche-Comté, Besançon, France

8. Department of Urology, Hôpital Europeen Georges-Pompidou (HEGP), AP-HP, Paris, France

9. Department of Urology, CHU Clermont-Ferrand, UMR1240 INSERM, Université Clermont-Auvergne, Clermont Ferrand, France

10. Department of Urology, Hôpital Europeen Georges-Pompidou (HEGP), AP-HP, INSERM, PARCC, Paris, France

Abstract

Aim: Comparison of the efficacy/safety/health-related quality of life of apalutamide, enzalutamide and darolutamide in Phase III clinical trials involving patients with nonmetastatic castration-resistant prostate cancer was performed. Materials & methods: Relevant studies were identified by searching PubMed as well as conference abstracts reporting updated overall survival. Three pivotal trials were identified, SPARTAN (apalutamide), PROSPER (enzalutamide) and ARAMIS (darolutamide), and form the basis of this analysis. Results: All three drugs significantly prolonged metastasis-free survival, prostate-specific antigen response and overall survival versus placebo, and were generally well tolerated. Conclusion: Drug selection will likely be influenced by tolerability/safety and other factors, such as the propensity for drug–drug interactions and the presence of comorbidities, that affect the risk–benefit balance in individual patients.

Publisher

Future Medicine Ltd

Subject

Cancer Research,Oncology,General Medicine

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