Assessment of Functional Status of Estrogen Receptors in Breast Cancer by Positron Emission Tomography

Breast Cancer Clinical Trial

Official title:

Assessment of Functional Status of Estrogen Receptors in Breast Cancer by Positron Emission Tomography

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02455453
• Other study ID #: 201411005
• Secondary ID: 5R01CA195450-03
• Status: Completed
• Phase: Phase 2
• Start date: April 28, 2015
• Est. completion date: January 3, 2019

Study information

• Verified date: January 2020
• Source: Washington University School of Medicine
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the uptake of a radioactive tracer 21-18F-fluoro-16α,17α-[(R)-(1'-α-furylmethylidene)dioxy]-19-norpregn-4-ene-3,20-dione (FFNP) uptake, which binds to breast cancer progesterone receptors (PgRs) on a PET/CT scan before and after administration of estradiol for one day (estrogen challenge) to determine if the change in uptake is a predictor of response to endocrine therapy (ET) in patients with hormone-sensitive estrogen receptor positive (ER+), human epidermal growth factor receptor 2-negative (HER2-) breast cancer. Estradiol is the most potent of the naturally occurring estrogens, and can be administered to treat menopausal symptoms and also sometimes to treat metastatic breast cancer. The investigators propose to study patients with biopsy-proven newly diagnosed, locally advanced, metastatic, or recurrent breast cancer who are going to be treated with endocrine therapy (ET) (tamoxifen,aromatase inhibitors or fulvestrant as standard of care therapy.

Subjects will undergo a total of two FFNP-PET/CT scans; one before and a second one immediately following the one day estradiol challenge before the start of standard of care ET. The estradiol challenge will consist of administering a total of 6 mg of estradiol orally (three doses of 2 mg each) given at approximately 8 hour intervals and over a 24 hour period.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 47
• Est. completion date: January 3, 2019
• Est. primary completion date: January 3, 2019
• Accepts healthy volunteers: No
• Gender: Female
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Patient must be postmenopausal defined as meeting one or more of the following:

• Age = 60 years

• Amenorrheic for at least 12 months

• Surgically sterile- having undergone bilateral oophorectomy,

• FSH level in postmenopausal range according to institutional standards (note follicle-stimulating hormone (FSH) laboratory testing must be ordered as standard of care to determine optimal treatment and should not be ordered simply to confirm eligibility to this study)

• OR Pre-menopausal for whom standard estradiol treatment (ET) is planned with ovarian suppression (imaging on study should be completed prior to start of ovarian suppression)

• Patient must have histological or cytological confirmed breast cancer and fall into one of the following categories:

• New diagnosis with plans for at least 6 months of neoadjuvant ET or any amount of neoadjuvant ET if surgery is planned as this will be used for response assessment .

• Patients with newly diagnosed metastatic breast cancer or patient with known metastatic disease who has progressed while on therapy (no washout period is needed if the patient was treated with AIs or chemotherapy, but 2 months washout period is needed if the patient was treated with tamoxifen) who are going to be treated with ET.

• Patient must have any one of the following types of breast cancer (primary or metastatic): ER+/PgR+/HER2- or ER+/PgR-/HER2-.

• ER+ is defined as Allred score of at least 4 and greater.

• PgR+ is defined as Allred score of at least 4 and greater.

• Immunohistochemistry (IHC) is the primary assay methodology for HER2. HER2- refers to HER2 of 0, 1+ by IHC or negative by fluorescence in situ hybridization (FISH)

• Patient must have at least one measurable lesion according to RECIST 1.1 by radiological evaluation (ultrasound, mammography, MRI, CT, PET) or physical examination.

• Patients with evaluable osseous metastasis that are lytic or mixed lytic-sclerotic are eligible.

• Patients with hepatic lesions may be eligible provided the location of the lesion is peripheral or not too close to hepatic ducts. Decision on hepatic lesion eligibility will be made by the principal investigator or sub-investigator after careful review of all available imaging to ensure evaluation of the lesion will not be obscured by normal hepatobiliary excretion of 18F-FFNP.

• Patient must be able to understand and willing to sign a written informed consent document.

• Prior chemotherapy or endocrine therapy is allowed

• The patient must have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-2 or, based on the judgment of the treating medical oncologist, can tolerate imaging and at least 6 months of ET

• The patient should have a life expectancy of > 6 months.

Exclusion Criteria:

• Patient with other invasive malignancies, with the exception of non-melanoma skin cancer or cervical carcinoma in-situ, who had (or have) any evidence of the other cancer present within the last 5 years

• Unable to tolerate up to 60 min of PET imaging per imaging session.

• Patients with non-measurable non-evaluable lesions such as pleural effusion are not eligible to participate.

• Patients with vertebral lesions that, in the opinion of the Principal Investigator and the treating medical oncologist, pose an imminent risk for cord compression.

Related Conditions & MeSH terms

• Breast Cancer
• Breast Neoplasms

Intervention

Drug:
• 18F-FFNP

Device:
• CTI/Siemens Biograph 40 PET/CT Scanner
Will include (1) 18-FDG-PET/CT scan Will include (2) 18F-FFNP-PET/CT scans

Drug:
• Estradiol

• 18F-FDG

Locations

Country	Name	City	State
United States	Washington University School of Medicine	Saint Louis	Missouri

Sponsors (2)

Lead Sponsor	Collaborator
Washington University School of Medicine	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in Primary Tumor FFNP Uptake Before and After Estradiol Challenge as Measured by Percent Change in Standardized Uptake Value (SUV)		Completion of second FFNP-PET/CT scan (up to 4 weeks)
Primary	Change in Secondary Tumor FFNP Uptake Before and After Estradiol Challenge as Measured by Percent Change in Standardized Uptake Value (SUV)		Completion of second FFNP-PET/CT scan (up to 4 weeks)
Secondary	Heterogeneity of Tumor FFNP Uptake as Measured by Number of Participants With Heterogenous Response	As measured visually in known lesion by recording presence or absence of uptake with note of any changes between scans	Completion of second FFNP-PET/CT scan (up to 4 weeks)

External Links

•   Alvin J. Siteman Cancer Center at Barnes-Jewish Hospital and Washington University School of Medicine