Radium-223
Conditions
Interventions
This registry aims to evaluate the efficacy of Radium-223 treatment in a non-study population of CRPC patients treated earlier with Docetaxel and patients not treated earlier with Docetaxel and effica
Sponsors
Netherlands Cancer Institute-Antoni van Leeuwenhoek hospital
Eligibility
Inclusion criteria
Inclusion criteria: 1. At the physicians discretion
Exclusion criteria
Exclusion criteria: 1. At the physicians discretion
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1.To evaluate the efficacy of Radium-223 treatment in a non-study population by effects on Symptomatic Skeletal Event (SSE) 2. Evaluate Radium-223 treatment efficacy by patient reported analgesic use and pain outcome | — |
Secondary
| Measure | Time frame |
|---|---|
| 1. Evaluate Radium-223 treatment efficacy in a non-study population of CRPC patients by clinical parameters. 2. Evaluate Radium-223 treatment tolerability in a non-study population of CRPC patients. 3. Evaluate the efficacy of the first subsequent therapy by clinical parameters 6. Identification of predictive clinical and explorative biomarkers of Radium-223 efficacy | — |
Contacts
Public ContactS.K. Badrising
Netherlands Cancer Institute (NKI-AvL)
Outcome results
None listed