2020
Efficacy and safety of vilaprisan in women with uterine fibroids: Data from the phase 2b randomized controlled trial ASTEROID 2
GEMZELL-DANIELSSON, Kristina, Oskari HEIKINHEIMO, Janos ZATIK, Robert POKA, Tomasz RECHBERGER et. al.Základní údaje
Originální název
Efficacy and safety of vilaprisan in women with uterine fibroids: Data from the phase 2b randomized controlled trial ASTEROID 2
Autoři
GEMZELL-DANIELSSON, Kristina (752 Švédsko), Oskari HEIKINHEIMO (246 Finsko), Janos ZATIK (348 Maďarsko), Robert POKA (348 Maďarsko), Tomasz RECHBERGER (616 Polsko), Robert HUDEČEK (203 Česká republika, domácí), Kathrin PETERSDORF (276 Německo), Francisco RAMIREZ (276 Německo), Thomas FAUSTMANN (276 Německo), Esther GROETTRUP-WOLFERS a Christian SEITZ (276 Německo, garant)
Vydání
EUROPEAN JOURNAL OF OBSTETRICS & GYNECOLOGY AND REPRODUCTIVE BIOLOGY, AMSTERDAM, ELSEVIER SCIENCE BV, 2020, 0301-2115
Další údaje
Jazyk
angličtina
Typ výsledku
Článek v odborném periodiku
Obor
30214 Obstetrics and gynaecology
Stát vydavatele
Německo
Utajení
není předmětem státního či obchodního tajemství
Odkazy
Impakt faktor
Impact factor: 2.435
Kód RIV
RIV/00216224:14110/20:00116813
Organizační jednotka
Lékařská fakulta
UT WoS
000573036000002
Klíčová slova anglicky
Vilaprisan; Heavy menstrual bleeding; Uterine fibroids; Amenorrhea; Selective progesterone receptor modulator
Příznaky
Mezinárodní význam, Recenzováno
Změněno: 11. 11. 2020 11:19, Mgr. Tereza Miškechová
Anotace
V originále
Objective: To assess the efficacy of vilaprisan compared with placebo in the management of the symptoms of uterine fibroids (UF), with a secondary objective to provide a descriptive comparison with ulipristal acetate. Study design: The randomized, parallel-group, double-blind, placeboand active-controlled, multicenter ASTEROID 2 trial assessed the efficacy and safety of vilaprisan versus placebo and ulipristal acetate for two 12-week treatment periods in women with >1 UF experiencing heavy menstrual bleeding (HMB). The primary endpoint compared the efficacy of vilaprisan with placebo at 12 weeks, assessed as the absence of bleeding/spotting by bleeding diary. Secondary endpoints compared the efficacy of vilaprisan with ulipristal acetate. Results of the first 12-week treatment period are reported here. Results: Women (mean age 42.5 years) were enrolled from 1 June 2015. At baseline, mean menstrual blood loss per 28 days was 214.1 mL and the volume of the three largest UF was 106.2 mL. In total, 155 women completed the initial 12-week treatment period. Complete absence of bleeding/spotting until the end of the 12-week treatment period was achieved by 62.9 % of women receiving vilaprisan versus 0.0 % with placebo (p < .001); 55.4 % of women treated with ulipristal acetate reported absence of bleeding/spotting. The predefined HMB response (80 mL and 50 % reduction from baseline during the last 28 days of treatment) was observed in 95.7 % of subjects treated with vilaprisan and 86.5 % of subjects treated with ulipristal acetate. Vilaprisan and ulipristal acetate treatment reduced the sum of the volume of the three largest UF by 29.9 % and 23.8 %, respectively, whereas an increase of 6.3 % was observed in the placebo group. No safety concerns, including multiple laboratory parameters, were identified. Conclusion: Daily administration of vilaprisan 2 mg induced amenorrhea, controlled bleeding, decreased UF size, and was well tolerated in women with HMB associated with UF. (C) 2020 Published by Elsevier B.V.