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Clinical Trial
. 2000 Apr-Jun;4(2):97-101.

Delayed oral estradiol combined with leuprolide increases endometriosis-related pain

Affiliations
Clinical Trial

Delayed oral estradiol combined with leuprolide increases endometriosis-related pain

B S Hurst et al. JSLS. 2000 Apr-Jun.

Abstract

Objectives: To determine if low-dose estrogen replacement can be added to GnRH agonist therapy after three months to reduce hypoestrogenic symptoms while allowing continued relief of pain in patients with endometriosis.

Materials and methods: Thirteen women with endometriosis and pain were treated with six months of leuprolide acetate in a prospective, randomized double-blind placebo controlled study. After three months of therapy, six subjects initiated oral estradiol 1 mg daily, and seven received an identical placebo.

Results: Dysmenorrhea improved in both groups, and dyspareunia significantly improved in the GnRH agonist plus placebo group. The mean pain scores of the oral estrogen group tended to be higher than the placebo group, and hot flushes tended to be less severe with estrogen treatment. However, differences observed between the study and placebo groups did not reach statistical significance.

Conclusion: In a prospective, randomized study, low-dose estrogen replacement increases endometriosis-related pain during GnRH agonist therapy. The study was terminated after the first 13 subjects due to the concerning trend toward recurrent symptoms in women who received oral estradiol during GnRH agonist therapy for endometriosis-related pain. With the trend toward increasing pain with estrogen add-back therapy, a larger study would not seem to be justifiable.

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Figures

Figure 1.
Figure 1.
Plots of the means and standard errors for dysmenorrhea. Week -4 indicates the pretreatment visit (time period one). Week 0 indicates the start of leuprolide therapy (time period two). Week 12 is the start of oral estradiol or placebo in addition to leuprolide (time period three).
Figure 2.
Figure 2.
Plots of the means and standard errors for dyspareunia. Week 4 indicates the pretreatment visit (time period one). Week 0 indicates the start of leuprolide therapy (time period two). Week 12 is the start of oral estradiol or placebo in addition to leuprolide (time period three).

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