A benefit-risk assessment of medical treatment for uterine leiomyomas

被引:32
作者
De Leo, V [1 ]
Morgante, G [1 ]
La Marca, A [1 ]
Musacchio, MC [1 ]
Sorace, M [1 ]
Cavicchioli, C [1 ]
Petraglia, F [1 ]
机构
[1] Univ Siena, Dept Pediat Obstet & Reprod Med, I-53100 Siena, Italy
关键词
D O I
10.2165/00002018-200225110-00002
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
The growth of a uterine leiomyoma stops and regresses after the menopause suggesting that leiomyoma growth is dependent on ovarian steroids. Therefore, estrogen has received much attention as the major factor responsible for the development of uterine leiomyomas, but progesterone also plays an important role in development of this disease. Cytogenetic analyses of resected samples has revealed that about 40 to 50% of leiomyomas show karyotypically detectable chromosomal abnormalities. Gonadotrophin releasing hormone (GnRH) agonists exert their action through the suppression of endogenous gonadotrophins and gonadal steroid secretion. Significant reductions of uterine/leiomyoma volume under GnRH agonist therapy has been reported in several studies. However, the leiomyoma generally returns to its pretreatment volume within a few months after discontinuation of the GnRH agonist. To minimise the adverse effects of hypoestrogenism during GnRH agonist treatment, add back therapy can be used (estrogen-progestin, progestin alone and recently tibolone). Antiprogestins have a potential clinical utility in uterine leiomyomas. Mifepristone is a synthetic steroid with both antiprogesterone and antiglucocorticoid activities, that may have an inhibitory effect on growth of leiomyoma. Danazol is an isoxazole of 17beta-ethinyl testosterone, a synthetic steroid, which has a suppressive effect on sex hormone binding globulin concentrations, resulting in efficacy in the short-term treatment of uterine leiomyomas. Gestrinone is a tri-enic steroid with antiestrogen and anti progesterone properties and has been shown to reduce uterine volume and stop bleeding. Growth factors play a relevant role on the pathophysiology of uterine leiomyoma and probably the inhibition of the action of growth factors on the myometrium will be the basis for future therapy. A number of agents are under investigation for treating uterine leiomyoma. Agents developed from increasing genetic knowledge of this condition could represent, in the next few years, new trends in the medical treatment of uterine leiomyomas.
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页码:759 / 779
页数:21
相关论文
共 139 条
  • [1] PURIFICATION, AMINO ACID COMPOSITION AND N-TERMINUS OF HYPOTHALAMIC LUTEINIZING HORMONE RELEASING FACTOR (LRF) OF OVINE ORIGIN
    AMOSS, M
    BURGUS, R
    BLACKWELL, R
    VALE, W
    FELLOWS, R
    GUILLEMIN, R
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1971, 44 (01) : 205 - +
  • [2] [Anonymous], 1998, Hum Reprod, V13, P3023
  • [3] BARBIERI RL, 1979, FERTIL STERIL, V31, P182
  • [4] BARBIERI RL, 1982, FERTIL STERIL, V37, P737
  • [5] DANAZOL INHIBITS HUMAN ADRENAL 21-HYDROXYLATION AND 11-BETA-HYDROXYLATION INVITRO
    BARBIERI, RL
    OSATHANONDH, R
    CANICK, JA
    STILLMAN, RJ
    RYAN, KJ
    [J]. STEROIDS, 1980, 35 (03) : 251 - 263
  • [6] DANAZOL INHIBITS STEROIDOGENESIS IN RAT TESTIS INVITRO
    BARBIERI, RL
    CANICK, JA
    RYAN, KJ
    [J]. ENDOCRINOLOGY, 1977, 101 (06) : 1676 - 1682
  • [7] BARBIERI RL, 1977, FERTIL STERIL, V28, P809
  • [8] BARBIERI RL, 1990, PROG CLIN BIOL RES, V323, P241
  • [9] BAULIEU EE, 1993, CLIN APPLICATIONS MI, P71
  • [10] BERAL V, 1990, BMJ-BRIT MED J, V300, P1229