Publication:
Efficacy and safety of ultra-low dose 0.005% estriol vaginal gel for the treatment of vulvovaginal atrophy in postmenopausal women with early breast cancer treated with nonsteroidal aromatase inhibitors: a phase II, randomized, double-blind, placebo-controlled trial.

dc.contributor.authorHirschberg, Angelica Lindén
dc.contributor.authorSánchez-Rovira, Pedro
dc.contributor.authorPresa-Lorite, Jesús
dc.contributor.authorCampos-Delgado, Miriam
dc.contributor.authorGil-Gil, Miguel
dc.contributor.authorLidbrink, Elisabet
dc.contributor.authorSuárez-Almarza, Javier
dc.contributor.authorNieto-Magro, Concepción
dc.date.accessioned2023-02-08T14:41:08Z
dc.date.available2023-02-08T14:41:08Z
dc.date.issued2020
dc.description.abstractTo assess the efficacy and safety of ultra-low dose 0.005% estriol vaginal gel in women with breast cancer receiving nonsteroidal aromatase inhibitors (NSAIs) and experiencing treatment-related vulvovaginal symptoms and signs. Women with hormone receptor-positive early breast cancer receiving NSAIs were randomized to either estriol vaginal gel or placebo for 12 weeks. Vaginal maturation, vaginal pH, and total and individual scores of symptoms and signs of vulvovaginal atrophy were assessed at baseline and at weeks 3 and 12; sexual functioning was also evaluated using the Female Sexual Functioning Index (FSFI) questionnaire, as well as circulating estrogens, follicle-stimulating hormone (FSH) and luteinizing hormone (LH). Sixty-one women with a mean age of 59 years were included: 50 received 0.005% estriol vaginal gel and 11 received placebo. Active treatment significantly improved maturation value and pH, vaginal dryness and global scores of symptoms and signs. Active treatment also increased the total FSFI score and all the FSFI domains, with the exception of pain. Small oscillations were observed in FSH and LH, which remained within the postmenopausal range. Estriol levels increased initially and normalized by week 12, and estradiol and estrone remained mostly undetectable throughout the study. Ultra-low dose 0.005% estriol vaginal gel showed efficacy in improving the symptoms and signs of vulvovaginal atrophy. These results, together with minimal oscillations in hormonal levels throughout the treatment, support the use of ultra-low dose 0.005% estriol vaginal gel as a treatment option for vulvovaginal atrophy in women with breast cancer receiving NSAIs with an indication for treatment with vaginal estrogens. : Video Summary:http://links.lww.com/MENO/A531.
dc.identifier.doi10.1097/GME.0000000000001497
dc.identifier.essn1530-0374
dc.identifier.pmcPMC7188038
dc.identifier.pmid32049923
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7188038/pdf
dc.identifier.unpaywallURLhttps://journals.lww.com/menopausejournal/Fulltext/2020/05000/Efficacy_and_safety_of_ultra_low_dose_0_005_.7.aspx
dc.identifier.urihttp://hdl.handle.net/10668/15093
dc.issue.number5
dc.journal.titleMenopause (New York, N.Y.)
dc.journal.titleabbreviationMenopause
dc.language.isoen
dc.organizationHospital Universitario de Jaén
dc.page.number526-534
dc.pubmedtypeClinical Trial, Phase II
dc.pubmedtypeJournal Article
dc.pubmedtypeRandomized Controlled Trial
dc.pubmedtypeResearch Support, Non-U.S. Gov't
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subject.meshAdministration, Intravaginal
dc.subject.meshAromatase Inhibitors
dc.subject.meshAtrophy
dc.subject.meshBreast Neoplasms
dc.subject.meshEstriol
dc.subject.meshEstrogens
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshMiddle Aged
dc.subject.meshPostmenopause
dc.subject.meshTreatment Outcome
dc.subject.meshVagina
dc.subject.meshVaginal Creams, Foams, and Jellies
dc.titleEfficacy and safety of ultra-low dose 0.005% estriol vaginal gel for the treatment of vulvovaginal atrophy in postmenopausal women with early breast cancer treated with nonsteroidal aromatase inhibitors: a phase II, randomized, double-blind, placebo-controlled trial.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number27
dspace.entity.typePublication

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