LH-RH agonist (Buserelin): treatment of endometriosis

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Buserelin treatment of endometriosis showed implant regression in 73% of patients, with a 40% pregnancy rate in infertile patients, and suppressed estradiol and progesterone, indicating anovulatory cycles.

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This study investigated intranasal LH-RH (GnRH) agonist buserelin in 64 patients with histologically verified endometriosis treated for 6 months at 900 μg/day. Follow-up surgery reported regression of endometriotic implants in 73% of cases, with adhesions appearing unaffected, and among 45 patients with prior infertility the uncorrected pregnancy rate was 40% while histology-confirmed recurrence was 9.4%. Endocrine testing showed marked estradiol suppression and progesterone decline consistent with anovulatory cycles, with decreased LH and prolactin but unchanged FSH; limited endocrine/bone-medicine markers (calcitonin and PTH fragments) and multiple metabolic panels showed no negative metabolic effects, while HDL increased and most subjective complaints were attributed to hypoestrogenism. This paper is centrally about endometriosis — evaluating buserelin’s effects on implant regression, recurrence, endocrine suppression, and side effects in treated patients.

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Abstract

To investigate the effects of the LH-RH agonist Buserelin [D-Ser (But)6 des-Gly10-LHRH ethylamide] on endometriosis, 64 patients were treated with 900 micrograms/d Buserelin intranasally over 6 months after histological verification of the disease. As shown by the follow-up operation at the end of treatment, 73% of cases showed regression of implants, whereas adhesions seemed to be unaffected. The uncorrected pregnancy rate of the 45 patients with a history of infertility was 40%, while the overall recurrence rate--confirmed by histological examination--was 9.4%. The endocrine parameters demonstrated a highly significant suppression of estradiol (E2) and a sharp decline of progesterone (Prog), indicating anovulatory cycles. Follicle-stimulating hormone (FSH) was unchanged, while luteinizing hormone (LH) and prolactin (Prl) decreased significantly. The androgenic parameters testosterone (T), dehydroepiandrosterone sulfate (DHEA-S), and sex-hormone-binding globulin (SHBG) revealed no relevant changes. Influence on bone metabolism could not be detected by measuring calcitonin and parathyroid hormone fragments (PTH-C and PTH-MM). Negative metabolic effects were absent in terms of hematology, clotting system, liver enzymes, renal parameters and lipid metabolism. Remarkable was a significant increase of high-density-lipoprotein cholesterol (HDL). Subjective complaints were mostly attributed to the therapy-induced hypoestrogenism. We consider Buserelin to be an effective drug in the treatment of endometriosis, with a low incidence of relevant side effects.
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Summary To investigate the effects of the LH-RH agonist Buserelin [D-Ser (But)6 des — Gly10 — LHRH ethylamide] on endometriosis, 64 patients were treated with 900 μg/d Buserelin intranasally over 6 months after histological verification of the disease. As shown by the follow-up operation at the end of treatment, 73% of cases showed regression of implants, whereas adhesions seemed to be unaffected. The uncorrected pregnancy rate of the 45 patients with a history of infertility was 40%, while the overall recurrence rate —confirmed by histological examination — was 9.4%. The endocrine parameters demonstrated a highly significant suppression of estradiol (E2) and a sharp decline of progesterone (Prog), indicating anovulatory cycles. Folliclestimulating hormone (FSH) was unchanged, while luteinizing hormone (LH) and prolactin (Prl) decreased significantly. The androgenic parameters testosterone (T), dehydroepiandrosterone sulfate (DHEA-S), and sex-hormone-binding globulin (SHBG) revealed no relevant changes. Influence on bone metabolism could not be detected by measuring calcitonin and parathyroid hormone fragments (PTH-C and PTH-MM). Negative metabolic effects were absent in terms of hematology, clotting system, liver enzymes, renal parameters and lipid metabolism. Remarkable was a significant increase of high-density-lipoprotein cholesterol (HDL). Subjective complaints were mostly attributed to the therapy — induced hypoestrogenism. We consider Buserelin to be an effective drug in the treatment of endometriosis, with a low incidence of relevannt side effects. Similar content being viewed by others References Abbasi R, Hodgen GD (1986) Predicting the predisposition to osteoporosis. JAMA 255:1600–1604 American Fertility Society (1979) Classification of endometriosis. 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AFS, p 2 Waibel S, Bremen T, Schiffl R, Scharla S, Wüster C, Ziegler R, Minne HW, Leyendecker G (1988) Bone density in patients treated with GnRH agonists for myomata and endometriosis. International Symposium on GnRH Analogues in Cancer and Human Reproduction, Geneva. (Gynecological endocrinology, vol 2) Parthenon, London, p 106 Author information Authors and Affiliations Rights and permissions About this article Cite this article Cirkel, U., Schweppe, K.W., Ochs, H. et al. LH-RH agonist (Buserelin): treatment of endometriosis. Arch Gynecol Obstet 246, 139–151 (1989). https://doi.org/10.1007/BF00934075 Received: Accepted: Issue date: DOI: https://doi.org/10.1007/BF00934075

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endometriosis

MeSH descriptors

Buserelin Endometriosis Uterine Neoplasms Buserelin Buserelin Endometriosis Female Gonadotropin-Releasing Hormone Gonadotropin-Releasing Hormone Humans Uterine Neoplasms

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