Background Cabergoline is a long-acting dopamine-agonist drugthat suppresses prolactin secretion and restores gonadal functionin women with hyperprolactinemic amenorrhea. We designed a studyto compare its safety and efficacy with those of bromocriptine,which has been the standard therapy.
Methods A total of 459 women with hyperprolactinemic amenorrheawere treated with either cabergoline (0.5 to 1.0 mg twice weekly)or bromocriptine (2.5 to 5.0 mg twice daily), administered ina double-blind fashion for 8 weeks and subsequently in an openfashion for 16 weeks, during which adjustments in the dose weremade according to the response. Of the 459 women, 279 had microprolactinomas,3 had macroprolactinomas, 1 had a craniopharyngioma, 167 hadidiopathic hyperprolactinemia, and the remainder had an emptysella. Clinical and biochemical status was assessed at 2-weekintervals for 8 weeks and monthly thereafter for a total of6 months, with an additional assessment at 14 weeks.
Results Stable normoprolactinemia was achieved in 186 of the223 women treated with cabergoline (83 percent) and 138 of the236 women treated with bromocriptine (59 percent, P<0.001).Seventy-two percent of the women treated with cabergoline and52 percent of those treated with bromocriptine had ovulatorycycles or became pregnant during treatment (P<0.001). Amenorrheapersisted in 7 percent of the cabergoline-treated women and16 percent of the bromocriptine-treated women. Adverse effectswere recorded in 68 percent of the women taking cabergolineand 78 percent of those taking bromocriptine (P = 0.03); 3 percentdiscontinued taking cabergoline, and 12 percent stopped takingbromocriptine (P<0.001) because of drug intolerance. Gastrointestinalsymptoms were significantly less frequent, less severe, andshorter-lived in the women treated with cabergoline.
Conclusions Cabergoline is more effective and better toleratedthan bromocriptine in women with hyperprolactinemic amenorrhea.
Source Information
From the Section of Endocrinology, Metabolism, and Diabetes, University of Wales College of Medicine, Cardiff, United Kingdom (J.W., I.I., M.F.S.); Pharmacia, Farmitalia Carlo Erba, Milan, Italy (G.P., A.P.); and the Endocrine Unit, Fatebenefratelli Hospital, Milan, Italy (C.I.F.). Members of the Cabergoline Comparative Study Group are listed in the Appendix.
Address reprint requests to Dr. Scanlon at the Department of Medicine, University of Wales College of Medicine, Heath Park, Cardiff CF4 4XN, Wales, United Kingdom.
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