FES (16α-[18F]-Fluoro-17β-estradiol)-PET: Towards a New Standard to Stage Locally Advanced and Recurrent, Estrogen Receptor Positive (ER+) Breast Cancer? Pilot Study to Compare [18F]FES-PET and [18F]FDG-PET

NCT03726931 | Completed DMC

• 1 other identifier: 2018.451
• Study Type: interventional
• Target: 40
• Locations: 1 country
• Sites: 1

Brief Summary

Accurate staging is of great importance in patients with clinically locally advanced primary breast cancer (LABC, stage III) or locoregional recurrent (LRR) breast cancer for making a correct treatment plan. According to current guidelines, staging is performed with positron emission tomography (PET) using the 2-\[18F\]fluoro-2-deoxy-D-glucose (\[18F\]FDG) PET tracer, combined with diagnostic computed tomography (CT). However, previous studies have shown that this technique (with the current PET tracer) might not be sufficient for accurate staging. Specifically in low grade, estrogen receptor positive (ER+) breast cancer metastases can be missed due to the low metabolic activity, leading to low uptake of \[18F\]FDG. Therefore, there is a clinical need to improve staging procedures. 16α-\[18F\]-fluoro-17β-estradiol (\[18F\]FES), an ER-targeted PET tracer, allows imaging of ER+ tumor lesions regardless of their metabolic activity. Patients with clinically LABC and LRR have a 25-50% risk of distant metastases. Correct identification of distant metastases allows adaptation of the treatment plan to avoid burdensome treatment with surgery, systemic and radiotherapy in order to maintain quality of life. In case of oligometastases, correct identification increases the likelihood for cure with local treatment. In the current study we will compare disease staging with \[18F\]FES- and \[18F\]FDG PET in patients with clinically LABC/LRR breast cancer. Objective: To determine whether \[18F\]FES PET/CT improves staging for women with clinically LABC or LRR, ER+/HER2- breast cancer as compared to standard \[18F\]FDG PET/CT. Study design: Multicenter prospective study with invasive measurements. Study population: 20 LABC and 20 LRR ER+/HER2- breast cancer patients. Main study parameters/endpoints: To determine the percentage of patients with a correctly changed treatment plan according to information obtained from \[18F\]FES PET/CT compared to \[18F\]FDG PET/CT at staging and at 6 months of follow-up; to determine the percentage of metastatic lesions detected and missed with \[18F\]FES PET/CT compared to \[18F\]FDG PET/CT (at staging and during follow-up). Nature and extent of the burden and risks associated with participation, benefit and group relatedness: Patients will receive an intravenous cannula for tracer injection and blood sampling, causing potentially transient discomfort at the site of the cannula insertion. Tumor biopsy will be performed from an easy accessible lesion and the most frequent complications that can occur are discomfort, bleeding and (local) infection. The risk of complications from a tumor biopsy is considered low: 0.24-1.6% and 0.11-0.48% for major complications and mortality, respectively. Radiation exposure from a \[18F\]FES PET and \[18F\]FDG PET scan usually ranges between 4-11 mSv and 7-8 mSv, respectively. Radiation exposure from a diagnostic CT scan ranges between 8-14 mSv. The total radiation burden is considered justifiable when compared to the information that can be obtained from this study, in this patient group with breast cancer. Imaging with \[18F\]FES PET may improve staging for patients with breast cancer as it may show tumor lesions that could not be identified with \[18F\]FDG PET, the current standard for staging. If this is the case, the initial treatment goal and intensity can be adjusted which can have beneficial effects for the patient.

Conditions

Breast Cancer

Outcome Measures

Primary Outcomes (4)

• Percentage of patients with a correctly changed treatment plan according to [18F]FES PET/CT compared to [18F]FDG PET/CT.

  Percentage of patients with a correctly changed treatment plan according to information obtained with \[18F\]FES PET/CT compared to \[18F\]FDG PET/CT at staging.

  2 years

• Percentage of metastatic lesions detected with [18F]FES PET/CT compared to [18F]FDG PET/CT.

  Percentage of metastatic lesions detected with \[18F\]FES PET/CT compared to \[18F\]FDG PET/CT at staging.

  2 years

• Percentage of missed metastases with [18F]FES PET/CT compared to [18F]FDG PET/CT.

  Percentage of missed metastases with \[18F\]FES PET/CT compared to \[18F\]FDG PET/CT (at staging and developed during follow-up).

  2 years

• Percentage of correct treatment plans as well as diagnostic confidence after 6 months of follow-up based on the added information obtained with [18F]FES PET/CT compared to [18F]FDG PET/CT.

  Percentage of correct treatment plans as well as diagnostic confidence after 6 months of follow-up as determined by the adjudication committee based on the added information obtained with \[18F\]FES PET/CT compared to \[18F\]FDG PET/CT.

  2 years

Secondary Outcomes (19)

• [18F]FES/[18F]FDG uptake related to size of the lesion

  2 years

• [18F]FES/[18F]FDG uptake related to location of the lesion.

  2 years

• [18F]FES/[18F]FDG uptake related to histological subtype.

  2 years

• [18F]FES/[18F]FDG uptake related to grade.

  2 years

• [18F]FES/[18F]FDG uptake related to ER expression level.

  2 years

Study Arms (1)

[18F]FES

EXPERIMENTAL

All patients will receive an additional PET/CT scan: \[18F\]FES PET/CT scan.

Diagnostic Test: 18F-Fluorestradiol PET/CT scan

Interventions

18F-Fluorestradiol PET/CT scan DIAGNOSTIC_TEST

\[18F\]FES PET/CT scan will be performed after administration of radioactive labelled estrogen.

Also known as: [18F]FES PET/CT scan

[18F]FES

Eligibility Criteria

• Age: 18 Years+
• Sex: female
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Clinically LABC (stage III) or LRR breast cancer (all histological types) with ER+, HER2- and low grade according to Bloom Richardson criteria (grade 1-2)
• Females aged 18 years or older at screening
• Eastern Cooperative Oncology Group Performance Status (ECOG PS) of 0-2
• In case \[18F\]FDG PET/CT has already been performed, patients can be included \<21 days after this scan
• Estimated glomerular filtration rate (eGFR) ≥30 ml/min
• Written and signed informed consent

You may not qualify if:

• History with another cancer within the last 5 years, except non-melanoma skin cancer
• Undergoing treatment for current breast cancer such as (neo)adjuvant chemotherapy, hormonal therapy (only in case of Tamoxifen), radiotherapy or investigational drug therapy
• Pregnancy or lactating women

Sponsors & Collaborators

• Amsterdam UMC, location VUmc: lead

Study Sites (1)

VU University Medical Center

Amsterdam, North Holland, Netherlands

Location

Related Publications (1)

• Iqbal R, Menke-van der Houven van Oordt CW, Oprea-Lager DE, Booij J. [18F]FES uptake in the pituitary gland and white matter of the brain. Eur J Nucl Med Mol Imaging. 2021 Aug;48(9):3009-3010. doi: 10.1007/s00259-021-05281-8. Epub 2021 Mar 17. No abstract available.

  PMID: 33730173 DERIVED

MeSH Terms

Conditions

Breast Neoplasms

Condition Hierarchy (Ancestors)

Neoplasms by Site; Neoplasms; Breast Diseases; Skin Diseases; Skin and Connective Tissue Diseases

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: DIAGNOSTIC
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: PRINCIPAL INVESTIGATOR
• PI Title: MD PhD, Medical Oncologist and Principal Investigator

Model Details: In this multicenter observational study with invasive measurements, patients with clinically ER+/HER2- LABC and LRR breast cancer will be included. All patients will undergo the current 'standard' diagnostic procedures including a histological biopsy of the primary tumor, cytology of axillary lymph nodes and imaging procedures with mammography, ultrasound of breast and axilla, magnetic resonance imaging (MRI) breast and whole body \[18F\]FDG PET combined with diagnostic chest/abdominal CT. In addition, all patients will undergo the 'experimental' imaging procedure with \[18F\]FES PET/CT. After evaluation of the obtained scans (independently for both scans), an 'experimental histological biopsy' of a lymph node metastasis will be obtained and clinically relevant \[18F\]FDG+ and/or \[18F\]FES+ lesions and/or suspicious lesions on CT will be biopsied according to standard clinical practice for pathological analyses.

Study Record Dates

• First Submitted: October 16, 2018
• First Posted: November 1, 2018
• Study Start: November 13, 2018
• Primary Completion: January 29, 2023
• Study Completion: January 29, 2023
• Last Updated: May 3, 2023

Record last verified: 2023-05

Locations

NL (1)