Vulvovaginal atrophy in women with and without a history of breast cancer: Baseline data from the PatiEnt satisfactiON studY (PEONY) in Italy.

Journal: Maturitas

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Affiliated Institutions:  IRCCS Azienda Ospedaliero-Universitaria di Bologna, Gynecology and Physiopathology of Human Reproduction, Bologna, Italy. Electronic address: cristina.meriggiola@unibo.it. Department of Obstetrics and Gynecology, Catholic University, Policlinico Universitario A. Gemelli IRCCS, Roma, Italy. Electronic address: paola.villa@unicatt.it. Department of Cardiovascular Endocrinology and Metabolism, Gynaecological and Cardiovascular Endocrinology and Osteoporosis Unit, "Gabriele Monasterio" Foundation and Italian National Research Council (CNR) Pisa, Pisa, Italy. Electronic address: silvia.maffei@ftgm.it. Section of Gynecology and Obstetrics, Department of Woman and Child Health, Careggi University Hospital, Florence, Italy. Electronic address: becorpia@aou-careggi.toscana.it. Shionogi S.r.l., Roma, Italy. Electronic address: t.dipaolantonio@shionogi.eu. CORESEARCH - Center for Outcomes Research and Clinical Epidemiology, Pescara, Italy. Electronic address: nicolucci@coresearch.it. Obstetrics and Gynaecology Department, IRRCS San Raffaele Hospital, Vita-Salute San Raffaele University, Milan, Italy. Electronic address: salvatore.stefano@hsr.it. Department of Clinical, Surgical, Diagnostic and Pediatric Sciences, University of Pavia, Pavia, Italy; Research Center for Reproductive Medicine and Gynecological Endocrinology - Menopause Unit, IRCCS S. Matteo Foundation, Pavia, Italy. Electronic address: nappi@rossellanappi.com.

Abstract summary 

To assess clinical characteristics of postmenopausal women with moderate/severe vulvovaginal atrophy, as well as its impact on sexual function, well-being, and quality of life, and to provide an overview of most used treatments.Ongoing longitudinal, observational study conducted in 17 Italian gynecology centers, involving women already treated or initiating a local vaginal estrogen therapy or ospemifene. We report baseline data for women with and without a history of breast cancer. Participants filled in self-reported questionnaires at study entry.Severity of vulvovaginal atrophy; ongoing treatments; patient-reported outcomes, including severity of symptoms, Day-to-Day Impact of Vaginal Aging (DIVA), Female Sexual Function Index (FSFI), Female Sexual Distress Scale-Revised (FSDS-R), and SF-12® Health Survey.Overall, 334 women (20.4 % with a history of breast cancer) started or continued local therapy (61.1 %) or ospemifene (38.8 %) at study entry. Vulvovaginal atrophy was severe in 28.6 %, and was responsible for severe symptoms, particularly vulvar dryness with burning or irritation and pain during sexual intercourse. Both sexual dysfunction (FSFI≤26) (81.5 %) and sexual distress (FSDS-R ≥ 11) (74.4 %) were common. A reduction in the SF-12 mental component score was documented. Women with breast cancer more often had severe vulvovaginal atrophy (41.2 %), had more severe symptoms, and the impact of vaginal symptoms on emotional well-being, sexual functioning and self-concept/body image was greater. The majority of them (83.8 %) received ospemifene as a treatment.Moderate/severe vulvovaginal atrophy is a common, often neglected condition with an impact on QoL and sexuality, particularly in women with a history of breast cancer. It is important to alleviate the burden associated with the disease.

Authors & Co-authors:  Meriggiola Villa Maffei Becorpi Di Paolantonio Nicolucci Salvatore Nappi

Study Outcome 

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Citations : 
Authors :  9
Identifiers
Doi : 10.1016/j.maturitas.2024.107950
SSN : 1873-4111
Study Population
Women,Female
Mesh Terms
Other Terms
Breast cancer;Local estrogens;Nonhormonal local treatments;Ospemifene;Vulvovaginal atrophy
Study Design
Study Approach
Country of Study
Publication Country
Ireland