Prostate cancer Cancer
Conditions
Interventions
This is an epidemiological, observational, multicentre, national study. A cohort of patients diagnosed with PCa in 2010 included in the ?Epidemiological study of the estimation of the incidence of PCa
Sponsors
Astelas Pharma S.A. (Spain)
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: Patient that was included in the study with code CaP01-10 with newly diagnosed, histopathologically confirmed PCa in any stage, between 1 January and 31 December 2010
Exclusion criteria
Exclusion criteria: Patients who have withdrawn their informed consent to take part in the study
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. Biochemical progression-free survival at 1, 2 and 3 years after being diagnosed in 2010 2. Clinical progression-free survival at 1, 2 and 3 years after being diagnosed in 2010 | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Patient?s clinical variables at the time of diagnosis associated with the 1 and 3 year survival 2. Therapeutic approach 3. Cancer-specific survival and overall survival | — |
Countries
Spain
Outcome results
None listed