Comparison endometrial of the efficacy and safety of two estradiol val e rate/d i enogest com bi nations and Kliogest" for continuous combined hormone replacement therapy in postmenopausal women

Objective To compare the efficacy and endometrial safety of two estradiol valeratel dienogest combinations with Kliogest@ in the treatment of postmenopausal symptoms. Design Methods Patients were randomized to estradiol valerate 2.0 mg/dienogest 2.0 mg (Climodien@), estradiol valerate 2.0 mgldienogest 3.0 mg (EZVal2DNG 3); or estradiol 2.0 mg/estriol 1.0 mghorethisterone acetate 1.0 mg (KliogesP) once daily for 1 year. The primary efficacy variable was the Kupperman index. Endometrial safety was determined primarily by biopsy. Results and Conclusions Climodien and E2Val 2/DNG 3 were therapeutically equivalent to Kliogest (mean changes in Kupperman index -20.1, -19.0 and -18.3, respectively). No statistically significant differences existed between treatment groups in the severity of postmenopausal symptoms. The incidences of endometrial atrophy were similar in all groups. Climodien appeared to be superior to Kliogest in terms of vaginal bleeding pattern, whereas E2Val2/DNG 3 was associated with a slightly higher incidence and greater intensity of vaginal bleeding. The incidences of adverse events were similar in all groups. A greater proportion of women in the Kliogest and E2Val 2/DNG 3 groups experienced vaginal bleeding, whereas breast problems were more common with Climodien. Climodien and EZVal 2/DNG 3 induced desirable changes in insulin-like growth factor I (decrease) and sex hormone binding globulin (increase) that were not seen with Kliogest. This was a double-blind, randomized, multicenter study.