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
  • [21] Pretreatment of Uterine Fibroids Using a Selective Progesterone Receptor Modulator - Ulipristal Acetate
    Thompson, M.
    Wong, M.
    Opemuyi, I.
    Madipola, N.
    Ramadan, T.
    Nnochiri, A.
    Guttman, J.
    20TH WORLD CONGRESS ON CONTROVERSIES IN OBSTETRICS, GYNECOLOGY & INFERTILITY (COGI), 2015, : 205 - 210
  • [22] Effect of a Selective Progesterone Receptor Modulator on Induction of Apoptosis in Uterine Fibroids In Vivo
    Horak, Petr
    Mara, Michal
    Dundr, Pavel
    Kubinova, Kristyna
    Kuzel, David
    Hudecek, Robert
    Chmel, Roman
    INTERNATIONAL JOURNAL OF ENDOCRINOLOGY, 2012, 2012
  • [23] Selective progesterone receptor modulators for fertility preservation in women with symptomatic uterine fibroids
    Ali, Mohamed
    Al-Hendy, Ayman
    BIOLOGY OF REPRODUCTION, 2017, 97 (03) : 337 - 352
  • [24] Selective Progesterone Receptor Modulator(ulipristal acetate - a new option in the pharmacological treatment of uterine fibroids in women
    Szamatowicz, Marian
    Kotarski, Jan
    GINEKOLOGIA POLSKA, 2013, 84 (03) : 219 - 222
  • [25] Predictive Factors of Response to Selective Progesterone Receptor Modulator (Ulipristal Acetate) in the Pharmacological Treatment of Uterine Fibroids
    Szydlowska, Iwona
    Marciniak, Aleksandra
    Nawrocka-Rutkowska, Jolanta
    Ryl, Aleksandra
    Starczewski, Andrzej
    INTERNATIONAL JOURNAL OF ENVIRONMENTAL RESEARCH AND PUBLIC HEALTH, 2020, 17 (03)
  • [26] The potential of selective progesterone receptor modulators for the treatment of uterine fibroids
    Bestel, Elke
    Donnez, Jacques
    EXPERT REVIEW OF ENDOCRINOLOGY & METABOLISM, 2014, 9 (01) : 79 - 92
  • [27] Functional evidence for two distinct mechanisms of action of progesterone and selective progesterone receptor modulator on uterine leiomyomas
    Milewska, Gabriela
    Ponikwicka-Tyszko, Donata
    Bernaczyk, Piotr
    Lupu, Oana
    Szamatowicz, Michal
    Sztachelska, Maria
    Pilaszewicz-Puza, Agata
    Koda, Mariusz
    Bielawski, Tomasz
    Zbucka-Kretowska, Monika
    Pawelczyk, Adam
    Tomaszewski, Jakub
    Li, Xiangdong
    Huhtaniemi, Ilpo
    Wolczynski, Slawomir
    Rahman, Nafis A.
    FERTILITY AND STERILITY, 2024, 122 (02) : 341 - 351
  • [28] Does the Selective Progesterone Receptor Modulator Ulipristal Normalize the Uterine Cavity in Women with Leiomyoma
    Levy, Gary
    Avila, Nilo
    Armstrong, Alicia Y.
    Nieman, Lynnette
    REPRODUCTIVE SCIENCES, 2011, 18 (03) : 95A - 95A
  • [29] Effects of Ulipristal Acetate, a Selective Progesterone Receptor Modulator, on Activin and Myostatin System Expression and Function in Uterine Leiomyoma
    Ciarmela, Pasquapina
    Carrarelli, Patrizia
    Islam, Md Soriful
    Tosti, Claudia
    Castellucci, Mario
    Petraglia, Felice
    REPRODUCTIVE SCIENCES, 2012, 19 (S3) : 159A - 160A
  • [30] A novel selective progesterone receptor modulator asoprisnil (J867) inhibits proliferation and induces apoptosis in cultured human uterine leiomyoma cells in the absence of comparable effects on myometrial cells
    Chen, W
    Ohara, N
    Wang, JY
    Xu, Q
    Liu, J
    Morikawa, A
    Sasaki, H
    Yoshida, S
    Demanno, DA
    Chwalisz, K
    Maruo, T
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2006, 91 (04): : 1296 - 1304