Buchholz S, Mögele M, Lintermans A, Bellen G, Prasauskas V, Ortmann O, Grob P, Neven P, Donders G
Department of Obstetrics and Gynecology, University Medical Center , Regensburg , Germany.
Climacteric. 2015 Apr;18(2):252-9. doi: 10.3109/13697137.2014.991301. Epub 2015 Jan 20.
We investigated the effect of a combination of vaginal ultra-low-dose estriol with lactobacilli on the sexual functioning domain of quality of life during the treatment of breast cancer survivors on an aromatase inhibitor with vaginal atrophy.
This was an open-label, bicentric, exploratory, clinical study in 16 postmenopausal breast cancer survivors on aromatase inhibitors suffering from vaginal atrophy-induced sexual disorders. Atrophy symptoms were assessed by scoring with an 11-point estimation scale (0 = not at all, 10 = worst imaginable feeling). Sexuality parameters of quality of life and medication adherence were recorded in a patient's diary and in the Female Somatic Sexual Experience Instrument (FSSEI) questionnaire. Patients underwent an initial treatment for 4 weeks (one vaginal tablet of Gynoflor(®) containing 0.03 mg estriol daily), followed by maintenance therapy (three vaginal Gynoflor(®) tablets weekly) for 8 weeks.
Vaginal dryness continuously improved from a median score of 8 at entry to a score of 4 at the end of initial therapy, and a median score of 2 at the end of maintenance therapy. Normal sexual activity before breast cancer diagnosis was reported by 14 women (88%). At study entry, only three women (19%) were sexually active. At the end of the Gynoflor(®) regimen, ten women (63%) reported sexual activity, of which seven (44%) reported sexual intercourse. The FSSEI demonstrated a non-significant trend of improvement of parameters related to sexuality.
Local vaginal therapy with Gynoflor(®) in breast cancer survivors on aromatase inhibitors reporting atrophic vaginitis could be considered as a useful treatment for the quality of sexual life.
我们研究了阴道超低剂量雌三醇与乳酸菌联合使用对接受芳香化酶抑制剂治疗且患有阴道萎缩的乳腺癌幸存者生活质量中性功能领域的影响。
这是一项开放标签、双中心、探索性临床研究,纳入了16名接受芳香化酶抑制剂治疗且患有阴道萎缩引起的性功能障碍的绝经后乳腺癌幸存者。通过11分评估量表(0 = 完全没有,10 = 可想象到的最严重感觉)对萎缩症状进行评分。生活质量的性参数和药物依从性通过患者日记以及女性躯体性体验量表(FSSEI)问卷进行记录。患者接受为期4周的初始治疗(每天阴道内使用1片含0.03 mg雌三醇的Gynoflor(®)),随后进行为期8周的维持治疗(每周阴道内使用3片Gynoflor(®))。
阴道干燥症状从中位数8分持续改善至初始治疗结束时的4分,维持治疗结束时的中位数为2分。14名女性(88%)报告在乳腺癌诊断前有正常的性活动。研究开始时,只有3名女性(19%)有性活动。在Gynoflor(®)治疗方案结束时,10名女性(63%)报告有性活动,其中7名(44%)报告有性交。FSSEI显示与性相关参数有非显著的改善趋势。
对于报告有萎缩性阴道炎的接受芳香化酶抑制剂治疗的乳腺癌幸存者,使用Gynoflor(®)进行局部阴道治疗可被视为改善性生活质量的有效治疗方法。