Targeting Progesterone Signaling for Breast Cancer Prevention in BRCA1 Carriers: a Pilot Study
Overview
- Phase
- Not Applicable
- Intervention
- Mifepristone 200 MG
- Conditions
- BRCA1 Mutation
- Sponsor
- Indiana University
- Locations
- 2
- Primary Endpoint
- Impact of mifepristone
- Status
- Withdrawn
- Last Updated
- 3 years ago
Overview
Brief Summary
The purpose of this study is to examine how a single dose of MIFEPREX® (mifepristone) affects the breast tissue in patients with BRCA1 (a gene that normally acts to restrain the growth of cells in the breast, but if it mutates may lead to breast cancer) mutations undergoing a planned prophylactic mastectomy (having one or both breasts removed).
Detailed Description
This is a single arm, prospective, observational trial enrolling up to 10 patients within Indiana University Simon Comprehensive Cancer Center. Eligible women will be consented to undergo breast biopsy 2-6 days prior to prophylactic mastectomy and take one dose of mifepristone 2 days prior to prophylactic mastectomy. If the initial biopsy is obtained on Day -2, the mifepristone should be taken AFTER the biopsy. Tissue from the ipsilateral breast will be taken at the time of mastectomy. Primary Objective To determine the impact of a single 200 mg dose of mifepristone on gene expression and metabolomic alterations in breast tissue of women with BRCA1 mutations who are planning prophylactic mastectomy.
Investigators
Tarah J Ballinger, MD
Assistant Professor Clinical Medicine
Indiana University
Eligibility Criteria
Inclusion Criteria
- •≥18 old at the time of informed consent
- •Known pathogenic germline BRCA1 mutation. The mutation must have been discovered by a CLIA- approved next generation sequencing panel (such as Myriad, Invitae, Ambry, etc) and confirmed by the PI.
- •Planning to undergo prophylactic risk reducing mastectomy
- •Premenopausal, defined as:
- •At least one ovary remains in situ, AND
- •Estradiol \> 20 or last menstrual period within the prior 3 months
- •Prior hysterectomy is allowed as long as at least one ovary remains in place
- •Must not be pregnant or nursing
- •a. Must have a negative urine pregnancy test for registration and between -6 to day -2 prior to receiving mifepristone
- •Ability to provide written informed consent and HIPAA authorization
Exclusion Criteria
- •Patients may not have used progesterone-only contraceptives (i.e. Depo- Provera) within the last 6 months. Combination estrogen/progesterone or estrogen only contraceptives are allowed.
- •Presence of an intrauterine device
- •Personal history of breast or ovarian cancer
- •Active heavy smoker, defined as 10 or more cigarettes per day on any occasion in the past 30 days
- •Uncontrolled chronic medical condition, including insulin dependent diabetes, NYHA class II, III or IV congestive heart failure, unstable angina, history of myocardial infarction, chronic pulmonary conditions including uncontrolled asthma (symptoms \> 2 days/week) or dyspnea requiring oxygen, peripheral vascular disease, symptomatic anemia, uncontrolled psychiatric conditions, chronic kidney disease, or liver disease (cirrhosis, NAFLD, etc.)
- •Requiring ongoing therapy with strong CYP3A4 inhibitor, steroids, or immunosuppressants (i.e. tacrolimus, cyclosporine, etc.). Please see appendix for full list of excluded co-medications. If questions, please ask the PI.
- •History of life- threatening allergic reaction to local anesthesia (lidocaine, xylocaine).
- •Contraindications including but not limited to allergic reactions to mifepristone or other prostaglandins, or inherited porphyrias
- •For the purposes of invasive breast biopsies, women must not be receiving therapeutic anticoagulation or antiplatelet agents
Arms & Interventions
mifepristone + surgery
Mifepristone is taken orally as a one-time only dose between 48 and 56 hours before your planned prophylactic mastectomy surgery
Intervention: Mifepristone 200 MG
mifepristone + surgery
Mifepristone is taken orally as a one-time only dose between 48 and 56 hours before your planned prophylactic mastectomy surgery
Intervention: Prophylactic mastectomy
Outcomes
Primary Outcomes
Impact of mifepristone
Time Frame: From baseline (day -2 to day -6) to Breast surgery (day 0)
To determine the impact of a single 200 mg dose of mifepristone on gene expression and metabolomic alterations in breast tissue of women with BRCA1 mutations.