C61
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: patients with prostate cancer (mestatsizing, castration resistent), who start a treatment with Cabazitaxel, Age over 18 years, patient informed consent
Exclusion criteria
Exclusion criteria: patient who participate in another study, earlier treatment with Cabazitaxel
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| The primary aim is the description of routine application of Cabazitaxel and foregoing/subsequent therapy options for treatment of patients with mCRPC in established doctor´s practices with emphasis on oncological urology. | — |
Secondary
| Measure | Time frame |
|---|---|
| The secondary aim is the description of through the medical evalued effectiveness including response, control of desease, progressionfree survival, time to therapy failure and overall survival. | — |
Countries
Germany
Contacts
OnkoDataMed GmbH