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Characterizing mechanisms of sensitivity and resistance to anti-androgen therapy with whole-body molecular imaging.

Predictive and prognostic value of 18F-prostate specific membrane antigen PET-CT and 18F-fluorodihydrotestosterone PET-CT in patients with metastatic castration-resistant prostate cancer treated with androgen biosynthesis inhibitors.

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON26005
Enrollment
50
Registered
2019-07-18
Start date
2019-04-01
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 castration-resistant prostate cancer

Interventions

None listed

Sponsors

Amsterdam UMC, location VUmc
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: 1. Histologically confirmed prostate cancer adenocarcinoma 2. Eligible for abiraterone treatment as judged by the treating physician. 3. Castrate levels of serum testosterone 4. Progressive disease manifest by either imaging (bone imaging, MRI, CT, or PSMA PET-CT) or biochemical progression (PSA). 5. Visible lesions on CT, bone imaging, MRI, or PSMA PET-CT consistent with disease.

Exclusion criteria

Exclusion criteria: 1. Previous anaphylactic reaction to either FDHT or PSMA.

Design outcomes

Primary

MeasureTime frame
Prognostic value of 18F-PSMA and FDHT imaging in men with mCRPC who will undergo AR-directed therapy.

Secondary

MeasureTime frame
Utility of 18F-PSMA and FDHT imaging as response indicator biomarkers for patients with mCRPC undergoing treatment with androgen biosynthesis inhibitors such as abiraterone.

Contacts

Public ContactMatthijs Cysouw

Amsterdam UMC, location VUmc

m.cysouw@amsterdamumc.nl+31-020-4444837

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)