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Androgen receptor and estrogen receptor imaging in metastatic breast cancer patients

Androgen receptor and estrogen receptor imaging in metastatic breast cancer patients - AR imaging metastatic breast cancer

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON39731
Enrollment
20
Registered
2013-11-13
Start date
2014-09-16
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

breast cancer

Interventions

PET scan (twice)

Sponsors

Universitair Medisch Centrum Groningen
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: 1. Metastatic breast cancer, with at least one known metastasis outside of the liver 2. Presence of a lesion that is safely accessible for tumor biopsy (may be liver lesion) 3. Postmenopausal status defined as one of the following: a. age >=60 years b. previous bilateral oophorectomy c. age 12 months in the absence of interfering hormonal therapies (such as LH-RH agonists and ER-antagonists) d. patients age 12 months and FSH >24 U/L and LH >14 U/L e. patient age

Exclusion criteria

Exclusion criteria: 1. Use of estrogen receptor ligands, including tamoxifen, fulvestrant or estrogens, or androgen receptor ligands, during the 6 weeks before entry into the study 2. Life-expectancy

Design outcomes

Primary

MeasureTime frame
The sensitivity and specificity of FDHT PET and FES PET to visualize and quantify AR- and ER-expression respectively, when compared to imunnohistochemistry on the biopsied metastasis.

Secondary

MeasureTime frame
- the heterogeneity of FDHT and FES uptake among metastases within an individual patient, as well as the inter-patient differences. - interobserver variation in PET interpretation between two independent observers from both study sites (VUMC and UMCG)

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)