Sexual dysfunction among gynecologic cancer survivors in a population-based cohort study

被引:0
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作者
Chun-Pin Chang
Christina M. Wilson
Kerry Rowe
John Snyder
Mark Dodson
Vikrant Deshmukh
Michael Newman
Alison Fraser
Ken Smith
Ankita Date
Joseph B. Stanford
David Gaffney
Kathi Mooney
Mia Hashibe
机构
[1] University of Utah School of Medicine,Division of Public Health, Department of Family and Preventive Medicine
[2] and Huntsman Cancer Institute,School of Nursing
[3] University of Alabama at Birmingham,Department of Obstetrics and Gynecology
[4] Intermountain Healthcare,Pedigree and Population Resource, Population Sciences
[5] University of Utah School of Medicine,Division of Public Health, Department of Family & Preventive Medicine
[6] University of Utah Health Sciences Center,Department of Radiation Oncology
[7] Huntsman Cancer Institute,College of Nursing, and Huntsman Cancer Institute
[8] University of Utah School of Medicine,undefined
[9] University of Utah School of Medicine,undefined
[10] and Huntsman Cancer Institute,undefined
[11] University of Utah,undefined
来源
Supportive Care in Cancer | 2023年 / 31卷
关键词
Sexual dysfunction; Sexual health; Gynecologic cancer; Ovarian cancer; Endometrial cancer; Cervical cancer; Survivors;
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摘要
Treatment for gynecologic cancer is associated with sexual dysfunction, which may present during and/or after treatment. The aim of this study was to investigate the risk of sexual dysfunction among gynecologic cancer survivors compared to cancer-free women in a population-based cohort study. We identified a cohort of 4863 endometrial, ovarian, and cervical cancer survivors diagnosed between 1997 and 2012 in the Utah Cancer Registry. Up to five cancer-free women were matched to cancer survivors (N = 22,693). We used ICD-9 codes to identify sexual dysfunction. Cox proportional hazards models were used to estimate hazard ratios (HRs) and 95% confidence intervals (CIs) for sexual dysfunction with adjustment for potential confounders. Approximately 6.6% of gynecologic cancer survivors had sexual dysfunction diagnoses 1–5 years after cancer diagnosis. Gynecologic cancer survivors had higher risks of overall sexual dysfunction (HR: 2.51, 95% CI: 2.16, 2.93), dyspareunia (HR: 3.27, 95% CI: 2.63, 4.06), and vaginal dryness (HR: 2.63, 95% CI: 2.21, 3.12) compared to a general population of women, 1–5 years after cancer diagnosis. Sexual dysfunction was associated with advance cancer stage (HRRegional vs. Localized: 1.61, 95% CI: 1.19, 2.31), radiation therapy (HR: 1.73, 95% CI: 1.29, 2.31), and chemotherapy (HR: 1.80, 95% CI: 1.30, 2.50). This large cohort study confirms that there is an increased risk of sexual dysfunction among gynecologic cancer survivors when compared to the general population. Further investigation is needed to address the risk factors for sexual dysfunction and to improve patient-provider communication, diagnosis, documentation, and treatment of sexual dysfunction among gynecologic cancer survivors.
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