BRCA1/2 and Effect of Mifepristone on the Breast
Study Details
Study Description
Brief Summary
Ovarian steroids, as well as their synthetic counterparts gestagens and estrogens have a role in breast cell proliferation and the development of breast cancer. Here, the effect of a progesterone receptor modulator, mifepristone, on cell proliferation in human breast tissue in vivo will be studied in women with BRCA-1 or -2 mutations. Our preliminary results implicate a possible protective effect of mifepristone in breast epithelium. The ability of mifepristone to block breast epithelial cell proliferation may prevent tumorigenesis and may also prove beneficial when used for contraceptive purposes and on other indications. The proposed project concerns a Randomized Controlled Trial on mifepristone versus placebo treatment of women with BRCA-1or -2 mutations with a high risk/incidence of breast cancer and ovarian cancer.
Condition or Disease | Intervention/Treatment | Phase |
---|---|---|
Phase 2 |
Detailed Description
Objectives • Research objective To study the safety and effect of treatment with mifepristone, a progesterone receptor modulator, on epithelial cell proliferation in human breast tissue in women with BRCA-1 or -2 mutations prior to protective mastectomy.
Project description
• Hypothesis/ Theory Mifepristone treatment exerts an antiproliferative, protective effect on breast tissue in women with BRCA-1 or -2 mutations
Study Design Randomized, double blind, placebo controlled trial. Women will be recruited among patients with BRCA-1 or -2 mutations scheduled for prophylactic mastectomy. Included women will be randomized to a 3-month treatment with mifepristone, 50 mg (Mifegyne, Exelgyn, Paris, France) or placebo taken orally every second day. Breast biopsies will be obtained in the luteal phase prior to start of treatment and again during surgery.
Study Design
Arms and Interventions
Arm | Intervention/Treatment |
---|---|
Experimental: Mifepristone treatment with oral mifepristone 50 mg every second day for 12 weeks in 30 women with BRCA 1 or 2 mutation |
Drug: Mifepristone
Randomised controlled trial of Mifepristone and placebo comparator Triobe
|
Placebo Comparator: TrioBe treatment with a quarter of a tablet of TrioBe every second day for 12 weeks |
Drug: Mifepristone
Randomised controlled trial of Mifepristone and placebo comparator Triobe
|
Outcome Measures
Primary Outcome Measures
- epithelial cell proliferation in breast tissue [3 months]
Changes from baseline after 12 weeks of mifepristone treatment in epithelial cell proliferation by measuring expression of genes specifically in the pathways involving apoptotic and cell proliferation by microarray study, including PTEN, Bcl-2 and Ki-67 along with steroid receptors.
Secondary Outcome Measures
- Vital signs and safety lab analysis [3 months]
Safety data includes vital signs, general- and gynecological-, incl breast - examinations, safety lab (hematology (blood status+CRP), kidney function (Na, K, krea) liver function (ASAT, ALAT, ALP, GT, bilirubin) , thyroid function (TSH,T3,T4), hormonal values FSH ,LH , PRL, SHBG, testosterone, E2 (sensitive) progesterone, urine dipstick and pregnancy test (prior to start). Endometrial histology will be investigated in biopsies obtained at baseline and at surgery. Women with BRCA-1/-2 mutations are followed according to the existing clinical routine with regard to ovarian cancer screening.
- Side effects and Adverse Events [3 months]
Side effects of mifepristone are mild and the only significant side effect reported in previous clinical trials with the same regimen has been mild flushes. All side effects and SAE/AE as well as any concomitant medication will be recoded by the participating patients in a dairy.
- Endometrial effects [3 months]
Bleeding patterns and endometrial morphologywill be studied. Endometrial histology and progesterone receptor modulator associated changes will be investigated in biopsies obtained at baseline and at surgery. Bleeding pattern will be registered during the study period by the participating women.
- Ovarian effects [3 months]
Women with BRCA-1/-2 mutations are followed according to the existing clinical routine with regard to ovarian cancer screening.
- Breast symptom evaluation [3months]
Breast symptom evaluation will be registered at baseline and during the study by a breast symptom score.
Eligibility Criteria
Criteria
Inclusion criteria:
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Pre-menopausal women, >/= 18 years of age
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with good general health and
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regular menstrual cycles (25-35 days) who are willing and
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able to participate after giving informed consent.
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women having BRCA1/2 mutation and have decided to undergo risk reducing mastectomy
Exclusion criteria includes:
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Any hormonal treatment used within 2 months prior to study start and
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Any contraindication to mifepristone
Contacts and Locations
Locations
Site | City | State | Country | Postal Code | |
---|---|---|---|---|---|
1 | Department of Woman and Child Health Karolinska University Hospital | Stockholm | Sweden | 17176 |
Sponsors and Collaborators
- Karolinska Institutet
Investigators
- Principal Investigator: Kristina Gemzell Danielsson, Professor, Dept of Womens and Childrens Health Karolinska Institutet
- Study Chair: Angelique Flöter Rådestad, MD PhD, Dept of Womens and Childrens Health, Karolinska Institutet
Study Documents (Full-Text)
None provided.More Information
Publications
- Engman M, Skoog L, Söderqvist G, Gemzell-Danielsson K. The effect of mifepristone on breast cell proliferation in premenopausal women evaluated through fine needle aspiration cytology. Hum Reprod. 2008 Sep;23(9):2072-9. doi: 10.1093/humrep/den228. Epub 2008 Jun 24.
- Isern AE, Loman N, Malina J, Olsson H, Ringberg A. Histopathological findings and follow-up after prophylactic mastectomy and immediate breast reconstruction in 100 women from families with hereditary breast cancer. Eur J Surg Oncol. 2008 Oct;34(10):1148-54. doi: 10.1016/j.ejso.2008.03.002. Epub 2008 Apr 23.
- Kauff ND, Brogi E, Scheuer L, Pathak DR, Borgen PI, Hudis CA, Offit K, Robson ME. Epithelial lesions in prophylactic mastectomy specimens from women with BRCA mutations. Cancer. 2003 Apr 1;97(7):1601-8.
- Poole AJ, Li Y, Kim Y, Lin SC, Lee WH, Lee EY. Prevention of Brca1-mediated mammary tumorigenesis in mice by a progesterone antagonist. Science. 2006 Dec 1;314(5804):1467-70.
- 2012-003703-35