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Endometriosetherapie mit Enantone®-Gyn Monats-Depot

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Leuprorelinacetat — Ein neues GnRH-Analogon

Zusammenfassung

Durch die rasche Entwicklung der verschiedenen Gonadotropin- Releasinghormon-Analoga (GnRH-Analoga) haben sich für die medikamentöse Behandlung der Endometriose neue Möglichkeiten ergeben. Die Gabe des GnRH-Analogons bewirkt einen reversiblen Hypoöstrogenismus durch die Down-Regulation der hypothalamisch- ovariellen Achse. In zahlreichen Studien konnte der günstige Einfluß von GnRH-Analoga auf die Endometriose dokumentiert werden [1–7]. In der vorliegenden, nicht vergleichenden, multizentrischen Phase-3-Studie wird über die Ergebnisse einer Untersuchung bei 104 Frauen mit Endometriose berichtet, die während einer Dauer von 6 Monaten mit dem GnRH-Analogon Leuprorelinacetat (Enantone®-Gyn Monats-Depot) behandelt wurden. Bei 70 dieser Patientinnen konnte bereits eine Follow-up-Periode von einem halben Jahr überblickt werden. Es war das Ziel dieser Studie, die Wirksamkeit, Sicherheit und Verträglichkeit von Leuprorelinacetat zu überprüfen.

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Literatur

  1. Shaw RW, Fraser HM, Boyle H (1983) Intranasal treatment with luteinising hormone releasing hormone agonist in women with endometriosis. Br Med J 287: 1667

    Article  CAS  Google Scholar 

  2. Lemay A, Maheux R, Faure N, Jean C, Fazekas ATA (1984) Reversible hypogonadism induced by a luteinizing hormone-releasing hormone ( LH-RH) agonist (buserelin) as a new therapeutic approach for endometriosis. Fertil Steril 41: 863–871

    PubMed  CAS  Google Scholar 

  3. Schriock E, Monroe SE, Heinzl M, Jaffe RB (1985) Treatment of endometriosis with a potent agonist ol gonadotropin-releasing hormone (nafarelin). Fertil Steril 44: 583–588

    PubMed  CAS  Google Scholar 

  4. Franssen AMHW, Rolland R, Chadha DR, Willemsen WNP, Vemer HM (1986) Treatment with a luteinising hormone-releasing hormone analogue (buserelin) in danazol-resistant endometriosis patients. Eur J Obstet Gynecol Reprod Biol 23: 379

    Article  PubMed  CAS  Google Scholar 

  5. Franssen AMHW, Kauer FM, Chadha DR, Zijlstra JA, Rolland R (1989) Endometriosis: treatment with gonadotropin-releasing hormone agonist Buserelin. Fertil Steril 51: 401–408

    PubMed  CAS  Google Scholar 

  6. Steingold KA, Cedars M, Lu JKH, Rändle D, Judd HL, Meldrum DR (1987) Treatment of endometriosis with a long acting gonadotropin-releasing hormone agonist. Obstet Gynecol 69: 403

    PubMed  CAS  Google Scholar 

  7. Henzl MR, Corson SL, Mohissi K, Buttram VC, Berqvist C, Jacobson J (1988) Administration of nasal nafarelin as compared with oral danazol for endometriosis. N Engl J Med 318: 485

    Article  PubMed  CAS  Google Scholar 

  8. The American Fertility Society (1985) Revised American Fertility Society classification of endometriosis: 1985. Fertil Steril 43: 351–352

    Google Scholar 

  9. Gerhard I, Bechtold E, Eggert-Kruse W, Heberling D, Runnebaum B (1990) Value of endometrial biopsies and serum hormone determinations in women with infertility. Hum Reprod 5: 906–914

    PubMed  CAS  Google Scholar 

  10. Gerhard I, Becker T, Eggert-Kruse W, Klinga K, Runnebaum B (1991) Thyroid and ovarian function in infertile women. Hum Reprod 6: 338–345

    PubMed  CAS  Google Scholar 

  11. Yamazaki I, Okada H (1980) A radioimmunoassay for a highly active luteinizing hormone-releasing hormone analogue and relation between the serum level of the analogue and that of gonadotropin. Endocrinol Jp 27: 593–605

    Article  CAS  Google Scholar 

  12. Dlugi AM, Miller JD, Knittle J (1990) Lupron depot (leuprolide acetate for depot suspension) in the treatment of endometriosis: a randomized, placebo- controlled, double-blind study. Fertil Steril 54: 419–427

    PubMed  CAS  Google Scholar 

  13. Dlugi AM, Rufo S, D’Amigo JF, Seibel MM (1988) A comparison of the effects of Buserelin versus danazol on plasma lipoproteins during treatment of pelvic endometriosis. Fertil Steril 49: 913–916

    PubMed  CAS  Google Scholar 

  14. Dmowski WP, Radwanska E, Binor Z, Tumman I, Pepping P (1989) Ovarian suppression induced with Buserelin or Danazol in the management of endometriosis. A randomized comparative study. Fertil Steril 51: 395–400

    PubMed  CAS  Google Scholar 

  15. Kiesel L, Thomas K, Tempone A, Trabant H, Widra W, Runnebaum B (1989) Efficacy and safety of Buserelin treatment in women with endometriosis — a multicentre open-label study. Gynecol Endocrinol 3 [Suppl 2]: 5–19

    Google Scholar 

  16. Johansen JS, Riis BJ, Hassager C, Moen M, Jacobson J. Christiansen C (1988) The effect of a gonadotropin-releasing hormone agonist analog (nafarelin) on bone metabolism. J Clin Endocrinol Metab 67: 701–706

    Article  PubMed  CAS  Google Scholar 

  17. Matta WH, Shaw RW, Hesp R, Evans R (1988) Reversible trabecular bone-density loss following induced hypoestrogenism with the GnRH analogue Buserelin in premenopausal women. Clin Endocrinol 29: 45–52

    Article  CAS  Google Scholar 

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© 1992 Springer-Verlag Berlin Heidelberg

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Gerhard, I., von Holst, T., Runnebaum, B. (1992). Endometriosetherapie mit Enantone®-Gyn Monats-Depot. In: Runnebaum, B., Breckwoldt, M. (eds) Leuprorelinacetat — Ein neues GnRH-Analogon. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-77666-3_6

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  • DOI: https://doi.org/10.1007/978-3-642-77666-3_6

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-540-55721-0

  • Online ISBN: 978-3-642-77666-3

  • eBook Packages: Springer Book Archive

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