Effects of the progesterone receptor modulator VA2914 in a continuous low dose on the hypothalamic-pituitary-ovarian axis and endometrium in normal women: a …
N Chabbert-Buffet, A Pintiaux-Kairis… - The Journal of Clinical …, 2007 - academic.oup.com
N Chabbert-Buffet, A Pintiaux-Kairis, P Bouchard
The Journal of Clinical Endocrinology & Metabolism, 2007•academic.oup.comContext: Progestin-only pills, the main hormonal alternative to ethinyl estradiol-containing
pills in women bearing vascular risk factors, are poorly tolerated due to irregular bleeding. In
contrast, progesterone receptor modulators can inhibit ovulation, alter endometrial
receptivity, and improve cycle control. Objective: We evaluated the effects of a new
progesterone receptor modulator, VA2914, administered continuously for 3 months, on
ovulation and endometrial maturation. Design, Settings, and Patients: Forty-six normal …
pills in women bearing vascular risk factors, are poorly tolerated due to irregular bleeding. In
contrast, progesterone receptor modulators can inhibit ovulation, alter endometrial
receptivity, and improve cycle control. Objective: We evaluated the effects of a new
progesterone receptor modulator, VA2914, administered continuously for 3 months, on
ovulation and endometrial maturation. Design, Settings, and Patients: Forty-six normal …
Abstract
Context: Progestin-only pills, the main hormonal alternative to ethinyl estradiol-containing pills in women bearing vascular risk factors, are poorly tolerated due to irregular bleeding. In contrast, progesterone receptor modulators can inhibit ovulation, alter endometrial receptivity, and improve cycle control.
Objective: We evaluated the effects of a new progesterone receptor modulator, VA2914, administered continuously for 3 months, on ovulation and endometrial maturation.
Design, Settings, and Patients: Forty-six normal women were included in a prospective, placebo-controlled, randomized trial, conducted in four referral centers.
Intervention: VA2914 (2.5, 5, or 10 mg/d) was administered continuously for 84 d. Pelvic ultrasound (treatment d 67 and 77), hormonal monitoring (FSH, LH, estradiol, and progesterone on treatment d 59, 63, 67, 70, 74, 77, 80, and 84), and endometrial biopsy (treatment d 77) were performed.
Main Outcome Measure: Ovulation inhibition was assessed by the absence of progesterone values above 3 ng/ml at any time during treatment month 3.
Results: Anovulation was observed in 81.8% women in the 5-mg group and 80% in the 10-mg group, and amenorrhea occurred in 81.2 and 90% of cases in the 5- and 10-mg groups. We did not detect any cases of endometrial hyperplasia despite estradiol levels that remained in the physiological follicular phase range throughout treatment cycle 3.
Conclusions: Continuous low-dose VA2914 can induce amenorrhea and inhibit ovulation without down-regulating estradiol levels or inducing endometrial hyperplasia in normal women. Long-term studies with a larger population are required to confirm the contraceptive efficacy of this regimen.
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