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Uterine fibroids: an update on current and emerging medical treatment options
Uterine fibroids are the most common gynecological disorder, classically requiring surgery when symptomatic. Although attempts at finding a nonsurgical cure date back to centuries, it is only around the middle of the last century that serious attempts at a medical treatment were carried out. Initial...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Dove Medical Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350833/ https://www.ncbi.nlm.nih.gov/pubmed/30774352 http://dx.doi.org/10.2147/TCRM.S147318 |
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author | Farris, Manuela Bastianelli, Carlo Rosato, Elena Brosens, Ivo Benagiano, Giuseppe |
author_facet | Farris, Manuela Bastianelli, Carlo Rosato, Elena Brosens, Ivo Benagiano, Giuseppe |
author_sort | Farris, Manuela |
collection | PubMed |
description | Uterine fibroids are the most common gynecological disorder, classically requiring surgery when symptomatic. Although attempts at finding a nonsurgical cure date back to centuries, it is only around the middle of the last century that serious attempts at a medical treatment were carried out. Initially, both progestins and estrogen–progestin combinations have been utilized, although proof of their usefulness is lacking. A major step forward was achieved when peptide analogs of the GnRH were introduced, first those with superagonist properties and subsequently those acting as antagonists. Initially, the latter produced side effects preventing their routine utilization; eventually, this problem was overcome following the synthesis of cetrorelix. Because both types of analogs produce hypoestrogenism, their use is limited to a maximum of 6 months and, for this reason, today they are utilized as an adjuvant treatment before surgery with overall good results. Over the last decade, new, nonpeptidic, orally active GnRH-receptor blockers have also been synthesized. One of them, Elagolix, is in the early stages of testing in women with fibroids. Another fundamental development has been the utilization of the so-called selective progesterone receptor modulators, sometimes referred to as “antiprogestins”. The first such compound to be applied to the long-term treatment of fibroids was Mifepristone; today, this compound is mostly used outside of Western Countries, where the substance of choice is Ulipristal acetate. Large clinical trials have proven the effectiveness of Ulipristal in the long-term medical therapy of fibroids, although some caution must be exercised because of the rare occurrence of liver complications. All selective progesterone receptor modulators produce unique endometrial changes that are today considered benign, reversible, and without negative consequences. In conclusion, long-term medical treatment of fibroids seems possible today, especially in premenopausal women. |
format | Online Article Text |
id | pubmed-6350833 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-63508332019-02-15 Uterine fibroids: an update on current and emerging medical treatment options Farris, Manuela Bastianelli, Carlo Rosato, Elena Brosens, Ivo Benagiano, Giuseppe Ther Clin Risk Manag Review Uterine fibroids are the most common gynecological disorder, classically requiring surgery when symptomatic. Although attempts at finding a nonsurgical cure date back to centuries, it is only around the middle of the last century that serious attempts at a medical treatment were carried out. Initially, both progestins and estrogen–progestin combinations have been utilized, although proof of their usefulness is lacking. A major step forward was achieved when peptide analogs of the GnRH were introduced, first those with superagonist properties and subsequently those acting as antagonists. Initially, the latter produced side effects preventing their routine utilization; eventually, this problem was overcome following the synthesis of cetrorelix. Because both types of analogs produce hypoestrogenism, their use is limited to a maximum of 6 months and, for this reason, today they are utilized as an adjuvant treatment before surgery with overall good results. Over the last decade, new, nonpeptidic, orally active GnRH-receptor blockers have also been synthesized. One of them, Elagolix, is in the early stages of testing in women with fibroids. Another fundamental development has been the utilization of the so-called selective progesterone receptor modulators, sometimes referred to as “antiprogestins”. The first such compound to be applied to the long-term treatment of fibroids was Mifepristone; today, this compound is mostly used outside of Western Countries, where the substance of choice is Ulipristal acetate. Large clinical trials have proven the effectiveness of Ulipristal in the long-term medical therapy of fibroids, although some caution must be exercised because of the rare occurrence of liver complications. All selective progesterone receptor modulators produce unique endometrial changes that are today considered benign, reversible, and without negative consequences. In conclusion, long-term medical treatment of fibroids seems possible today, especially in premenopausal women. Dove Medical Press 2019-01-23 /pmc/articles/PMC6350833/ /pubmed/30774352 http://dx.doi.org/10.2147/TCRM.S147318 Text en © 2019 Farris et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Review Farris, Manuela Bastianelli, Carlo Rosato, Elena Brosens, Ivo Benagiano, Giuseppe Uterine fibroids: an update on current and emerging medical treatment options |
title | Uterine fibroids: an update on current and emerging medical treatment options |
title_full | Uterine fibroids: an update on current and emerging medical treatment options |
title_fullStr | Uterine fibroids: an update on current and emerging medical treatment options |
title_full_unstemmed | Uterine fibroids: an update on current and emerging medical treatment options |
title_short | Uterine fibroids: an update on current and emerging medical treatment options |
title_sort | uterine fibroids: an update on current and emerging medical treatment options |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6350833/ https://www.ncbi.nlm.nih.gov/pubmed/30774352 http://dx.doi.org/10.2147/TCRM.S147318 |
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