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Metastatic hormone-sensitive and castration resistant prostate cancer registry: CAPRI 3.0

Metastatic hormone-sensitive and castration resistant prostate cancer registry: CAPRI 3.0

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON24783
Enrollment
10000
Registered
2021-03-16
Start date
2021-01-01
Completion date
Unknown
Last updated
2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Metastatic hormone-sensitive and castration resistant prostate cancer.

Interventions

None.

Sponsors

Radboud University Medical Center
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: Patients who were treated in a participating hospital after 01-01-2016 and have: - metastatic HSPC, defined as involvement of lymph nodes, bones or viscera on radiological assessment or as defined by either the treating doctor/physician (i.e. palliative treatment with surgical or medical castration) - metastatic CRPC, defined by the treating doctor/physician or the definition of the European Urology Association (EAU)[10], as prostate cancer that is progressing despite medical or surgical castration (i.e. castrate levels of testosterone (= 50 ng/dL or <1.7 nmol/L)

Exclusion criteria

Exclusion criteria: None.

Design outcomes

Primary

MeasureTime frame
The main objective is to assess effectiveness, efficiency and quality of treatments in HSPC and CRPC patients in the Netherlands.

Secondary

MeasureTime frame
- To describe the population of HSPC and CRPC patients; - To assess treatment patterns and outcomes of systemic anti-cancer treatment in HSPC and CRPC; - Focus on systemic treatment (including hormonal therapy, chemotherapy, bone directed therapy, immunotherapy, targeted therapy), radiotherapy, radionuclides and surgery; - Focus on relevant and readily available outcomes (including overall survival, treatment duration, biochemical response, severe adverse events); - To assess guideline adherence of diagnostic evaluation and anti-cancer treatment; - To assess access of patients to treatment innovations, mainly clinical trials and new treatment options; - To evaluate differences in real-world populations and trial populations.

Contacts

Public ContactDianne Bosch

Radboudumc

dianne.bosch@radboudumc.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)