Prostate Cancer Clinical Trial
Official title:
A Phase IV, Multicenter, National, Non-comparative, Open-label Study of Cabazitaxel, Combined With Prednisone and Prophylaxis of Neutropenia Complications in the Second-line Treatment of Patients With Metastatic Castration-resistant Prostate Cancer and After Failure of Docetaxel-based Chemotherapy. Descriptive Assessment of the Circulating Tumor Cells in This Context.
Primary Objective:
- To assess effectiveness of prophylactic treatment of hematological complications (grade ≥
3 neutropenia) resulting from cabazitaxel treatment for 21 days after treatment initiation.
Secondary Objectives:
- PSA response rate;
- Descriptive assessment of CTC (circulating Tumor Cells);
- Rates of grade ≥ 3 neutropenia and febrile neutropenia and grade ≥3 diarrhea over the
treatment period;
- Description of the Health Quality of Life of the patients;
- Incidence of adverse events.
Screening: 15 days Treatment: until disease progression Post-treatment Follow-up: 12 months ;
Endpoint Classification: Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment
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