Dynamic and Test-retest Whole Body [18F]FES PET Imaging in Patients With Metastatic ER+ Breast Cancer

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

16a-18F-fluoro-17b-estradiol (\[18F\]FES) is radioactive labeled estradiol, developed for in vivo visualization of the estrogen receptor (ER) using positron emission tomography (PET). To date, \[18F\]FES PET has been mainly explored as a diagnostic imaging tool to assess ER expression, thereby identifying locations of disease and their potential sensitivity to endocrine therapy, respectively. The primary aim of this project is to extend the application of \[18F\]FES PET as a baseline diagnostic imaging biomarker for ER expression to use it as an (early) treatment response marker. However, for such an application, visual assessment alone may not be sufficient and a more rigorous quantitative image analysis is needed. Therefore, in this project we shall first derive the optimal pharmacokinetic model for full quantitative analysis of \[18F\]FES uptake and, subsequently, we shall assess the validity of simplified, clinically feasible, quantitative parameters of \[18F\]FES uptake in 5 patients with metastatic estrogen receptor positive (ER+) breast cancer (part A). In addition, the repeatability of these simplified parameters will then be investigated in another 10 patients (part B).

Eligibility
Participation Requirements
Sex: Female
Minimum Age: 18
Healthy Volunteers: f
View:

• Histologically proven metastatic ER+ (\>10% positive stained cells using immunohistochemistry) breast cancer on the latest biopsy

• Postmenopausal females aged 18 years or older at screening. Postmenopausal status is defined as one of the following:

‣ age ≥60 years

⁃ age \<60 years and amenorrhea for \>12 months in the absence of interfering hormonal therapies (such as LH-RH agonists and ER-antagonists)

⁃ patient age \<60 years using LH-RH agonists should continue LH- RH-agonists until after the PET procedures

⁃ previous bilateral oophorectomy or medically confirmed ovarian failure

• \[18F\]FDG PET, CT and/or a bone scan should be performed as part of routine clinical staging (≤4 weeks prior to screening)

• Patients should have metastases in the scanning field of view, all located outside of the liver

• Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0-2

• Estimated glomerular filtration rate (eGFR) ≥30 ml/min

• Written and signed informed consent

Locations
Other Locations
Netherlands
Amsterdam UMC - location VUmc
RECRUITING
Amsterdam
Contact Information
Primary
Catherina W Menke-van der Houven van Oordt, MD PhD
dm-onco@amsterdamumc.nl
+31 (0)20 4444 773
Backup
Data-management Medical Oncology
dm-onco@amsterdamumc.nl
+31 (0)20 4444 773
Time Frame
Start Date: 2021-10-11
Estimated Completion Date: 2025-04
Participants
Target number of participants: 15
Treatments
Experimental: Part A: dynamic FES PET imaging
All patients included in part A will receive a dynamic FES PET/CT scan.
Experimental: Part B: whole body static FES PET imaging
All patients included in part B will receive a whole body static FES PET/CT scan twice within 1 week.
Related Therapeutic Areas
Sponsors
Leads: Amsterdam UMC, location VUmc

This content was sourced from clinicaltrials.gov