Selective Progesterone Receptor Modulators for the Medical Treatment of Uterine Fibroids with a Focus on Ulipristal Acetate

Author:

Rabe Thomas1ORCID,Saenger Nicole2,Ebert Andreas D.3ORCID,Roemer Thomas4,Tinneberg Hans-Rudolf5,De Wilde Rudy Leon6ORCID,Wallwiener Markus7

Affiliation:

1. Deutsche Gesellschaft für Gynäkologische Endokrinologie und Fortpflanzungsmedizin, Germany

2. Klinikum für Frauenheilkunde und Geburtshilfe, Frankfurt/M, Germany

3. Praxis für Frauengesundheit, Gynäkologie und Geburtshilfe-Endometriosezentrum Berlin, Germany

4. Evangelisches Krankenhaus Weyertal gGmbH, Köln, Germany

5. Universitätsklinik Gießen und Marburg, Campus Gießen, Germany

6. Klinik für Frauenheilkunde, Geburtshilfe und Gynäkologische Onkologie; Universitätsklinik für Gynäkologie, Pius-Hospital Oldenburg, Germany

7. Universitäts-Frauenklinik Heidelberg, Germany

Abstract

Uterine fibroids are the most frequent benign tumours in women of child-bearing age. Their symptoms are diverse and the quality of life of the women affected can be significantly impaired. While treatment to date has been primarily by means of surgical intervention, selective progesterone receptor modulators (SPRMs) open up new medication-based treatment options. EMA’s Pharmacovigilance Risk Assessment Committee (PRAC) has recently completed its review of ESMYA® (ulipristal acetate, 5 mg), following reports of serious liver injury, including liver failure leading to transplantation in postmarketing settings. We will provide some information on the PRAC’s recommendations to minimize this risk. Nevertheless, the effectiveness and safety of the SPRM ulipristal acetate (UPA), both with regard to preoperative administration and with regard to an intermittent administration as long-term treatment for patients with symptomatic uterine fibroids, have been shown in several clinical studies (PEARL I–IV).

Publisher

Hindawi Limited

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine

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