The effects of the selective progesterone receptor modulator asoprisnil on the morphology of uterine tissues after 3 months treatment in patients with symptomatic uterine leiomyomata

被引:102
|
作者
Williams, A. R. W.
Critchley, H. O. D.
Osei, J.
Ingamells, S.
Cameron, I. T.
Han, C.
Chwalisz, K.
机构
[1] Univ Edinburgh, Royal Infirm Edinburgh, Dept Pathol, Edinburgh EH16 4SA, Midlothian, Scotland
[2] Univ Edinburgh, Ctr Reprod Biol, Queens Inst Med Res, Edinburgh EH3 9EW, Midlothian, Scotland
[3] Univ Southampton, Princess Anne Hosp, DOHaD Div, Southampton, Hants, England
[4] TAP Pharmaceut Prod Inc, Lake Forest, IL USA
关键词
asoprisnil; cell-proliferation; endometrium; histopathology; progesterone receptor;
D O I
10.1093/humrep/dem026
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Asoprisnil is a selective progesterone receptor modulator with mixed progesterone agonist/antagonist activity which controls uterine bleeding via an endometrial effect. This study examined full-thickness endometrial, leiomyoma and myometrial morphology in hysterectomy specimens from patients with uterine leiomyomata, after treatment with asoprisnil for 3 months. METHODS: In this double-blind, randomized, placebo-controlled study, 33 subjects with uterine leiomyomata were randomized to receive asoprisnil 10, 25 mg or placebo for an average of 95 days prior to hysterectomy. Samples of endometrium, myometrium anti leiomyoma tissue were subjected to systematic morphological assessment with quantification of mitotic activity. RESULTS: In patients treated with 10 or 25 mg asoprisnil, a unique pattern called 'non-physiologic secretory effect' was evident in endometrium, recognizable through partially developed secretory glandular appearances and stromal changes. Endometrial thickness was decreased, and there were low levels of mitotic activity in endometrial glands and stroma. Unusual thick-walled muscular arterioles and prominent aggregations of thin-walled vessels were present in endometrial stroma, but not in myometrium or non-endometrial vascular beds. Mitotic activity was decreased in leiomyomata. CONCLUSIONS: Asoprisnil induces unique morphological changes and is associated with low levels of glandular and stromal proliferation in endometrium, and in leiomyomata. These changes are likely to contribute to the amenorrhoea experienced after exposure to the medication.
引用
收藏
页码:1696 / 1704
页数:9
相关论文
共 50 条
  • [41] Selective progesterone receptor modulator asoprisnil down-regulates collagen synthesis in cultured human uterine leiomyoma cells through up-regulating extracellular matrix metalloproteinase inducer
    Morikawa, Akira
    Ohara, Noriyuki
    Xu, Qin
    Nakabayashi, Koji
    DeManno, Deborah A.
    Chwalisz, Kristof
    Yoshida, Shigeki
    Maruo, Takeshi
    HUMAN REPRODUCTION, 2008, 23 (04) : 944 - 951
  • [42] Selective progesterone receptor modulator development and use in the treatment of leiomyomata and endometriosis (vol 26, pg 423, 2005)
    Chwalisz, K
    Perez, MC
    DeManno, D
    Winkel, C
    Schubert, G
    Elger, W
    ENDOCRINE REVIEWS, 2005, 26 (05) : 703 - 703
  • [43] Safety and efficacy of the selective progesterone receptor modulator asoprisnil for heavy menstrual bleeding with uterine fibroids: pooled analysis of two 12-month, placebo-controlled, randomized trials
    Stewart, E. A.
    Diamond, M. P.
    Williams, A. R. W.
    Carr, B. R.
    Myers, E. R.
    Feldman, R. A.
    Elger, W.
    Mattia-Goldberg, C.
    Schwefel, B. M.
    Chwalisz, K.
    HUMAN REPRODUCTION, 2019, 34 (04) : 623 - 634
  • [44] Markers of Cellular Proliferation, Apoptosis, Estrogen/Progesterone Receptor Expression and Fibrosis in Selective Progesterone Receptor Modulator (Ulipristal Acetate)-Treated Uterine Fibroids
    Szydlowska, Iwona
    Grabowska, Marta
    Nawrocka-Rutkowska, Jolanta
    Piasecka, Malgorzata
    Starczewski, Andrzej
    JOURNAL OF CLINICAL MEDICINE, 2021, 10 (04) : 1 - 13
  • [45] The effects of 1-month administration of asoprisnil (J867), a selective progesterone receptor modulator, in healthy premenopausal women
    Chwalisz, K
    Elger, W
    Stickler, T
    Mattia-Goldberg, C
    Larsen, L
    HUMAN REPRODUCTION, 2005, 20 (04) : 1090 - 1099
  • [46] Selective Progesterone Receptor Modulators for the Medical Treatment of Uterine Fibroids with a Focus on Ulipristal Acetate
    Rabe, Thomas
    Saenger, Nicole
    Ebert, Andreas D.
    Roemer, Thomas
    Tinneberg, Hans-Rudolf
    De Wilde, Rudy Leon
    Wallwiener, Markus
    BIOMED RESEARCH INTERNATIONAL, 2018, 2018
  • [47] The selective progesterone receptor modulator CDB4124 inhibits proliferation and induces apoptosis in uterine leiomyoma cells
    Luo, Xia
    Yin, Ping
    Coon, John S.
    Cheng, You-Hong
    Wiehle, Ronald D.
    Bulun, Serdar E.
    FERTILITY AND STERILITY, 2010, 93 (08) : 2668 - 2673
  • [48] Selective Progesterone Receptor Modulatores for uterine fibroid treatment - the statement of the Polish Gynecological Society Experts
    Debski, Romuald
    Kotarski, Jan
    Paszkowski, Tomasz
    Poreba, Ryszard
    Skrzypulec-Plinta, Violetta
    Spaczynski, Marek
    Szumilo, Justyna
    GINEKOLOGIA POLSKA, 2012, 83 (07) : 555 - 557
  • [49] The Selective Progesterone Receptor Modulator CDB4124 Inhibits Proliferation and Induces Apoptosis in Uterine Leiomyoma Cells.
    Luo, Xia
    Yin, Ping
    Coon, John S.
    Cheng, You-Hong
    Bulun, Serdar E.
    REPRODUCTIVE SCIENCES, 2010, 17 (03) : 271A - 271A
  • [50] Effects of levonorgestrel-releasing IUS and progesterone receptor modulator PRM CDB-2914 on uterine leiomyomas
    Maruo, Takeshi
    Ohara, Noriyuki
    Matsuo, Hiroya
    Xu, Qin
    Chen, Wei
    Sitruk-Ware, Regine
    Johansson, Elof D. B.
    CONTRACEPTION, 2007, 75 (06) : S99 - S103