Background: Uterine fibroids represent the leading indication for roughly 600,000 hysterectomies performed annually in the United States. There is no satisfactory long-term medical therapy for fibroids, which disproportionately affect black women. Preliminary data from our open label study show that oral administration of mifepristone 5 mg per day is associated with significant improvement in fibroid symptoms and nearly 50% reduction in fibroid size. However, findings from this study were limited by absence of a placebo control group, absence of blinding, and absence of a validated, disease-specific quality of life outcome measure.
Aims : We propose a six-month randomized, double-blinded, placebo-controlled trial of low-dose mifepristone. Seventy women with moderate to severely symptomatic fibroids, confirmed by ultrasonography, will be randomly allocated to receive mifepristone 5 mg per day or an identical appearing placebo. The primary outcome measure will be change in disease-specific quality of life based on the recently validated Uterine Fibroid Symptom Quality of Life questionnaire. Secondary outcomes include change in global health status, fibroid size, pain, bleeding, and adverse effects including endometrial hyperplasia. We also propose to test the hypothesis that administration of mifepristone will be associated with significant reductions in fibroid blood flow, which in turn, will be associated with reductions in fibroid volume. Significance: The study offers the promise for a safe, effective medical treatment for symptomatic fibroids that could potentially benefit millions of women world-wide, prevent thousands of hysterectomies and reduce health care costs. The study may also offer valuable insight into a mechanism by which mifepristone reduces fibroid size.

Agency
National Institute of Health (NIH)
Institute
Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD)
Type
Research Project (R01)
Project #
1R01HD042578-01A1
Application #
6616933
Study Section
Reproductive Endocrinology Study Section (REN)
Program Officer
Parrott, Estella C
Project Start
2003-07-25
Project End
2005-05-31
Budget Start
2003-07-25
Budget End
2004-05-31
Support Year
1
Fiscal Year
2003
Total Cost
$273,516
Indirect Cost
Name
University of Rochester
Department
Family Medicine
Type
Schools of Dentistry
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Fiscella, Julietta; Bonfiglio, Thomas; Winters, Paul et al. (2011) Distinguishing features of endometrial pathology after exposure to the progesterone receptor modulator mifepristone. Hum Pathol 42:947-53
Feng, Changyong; Meldrum, Sean; Fiscella, Kevin (2010) Improved quality of life is partly explained by fewer symptoms after treatment of fibroids with mifepristone. Int J Gynaecol Obstet 109:121-4
Fiscella, Kevin; Eisinger, Steven H; Meldrum, Sean et al. (2006) Effect of mifepristone for symptomatic leiomyomata on quality of life and uterine size: a randomized controlled trial. Obstet Gynecol 108:1381-7