Department of Medical Oncology, School of Medicine, Tekirdag Namik Kemal University, Tekirdağ, Turkey.
Department of Medical Oncology, School of Medicine, Marmara University, Istanbul, Turkey.
Support Care Cancer. 2023 May 10;31(6):330. doi: 10.1007/s00520-023-07791-7.
The primary aim of this study was to compare tamoxifen versus aromatase inhibitors (AI) in terms of urinary incontinence (UI) in premenopausal female patients receiving adjuvant hormone therapy for breast cancer. A secondary aim was to investigate the prevalence and the affecting factors of UI.
This study was designed as a multicenter, cross-sectional that included consecutive premenopausal breast cancer patients ≤50 years of age receiving tamoxifen (with/without LHRHa) or AI (with LHRHa) for at least 6 months, between June 2021 and September 2022. Patients with urinary incontinence before hormone treatments and metastatic patients were excluded from the study. Turkish validation of The International Consultation on Incontinence Modular Questionnaire Urinary Incontinence Short Form (ICIQ UI-SF) was used to determine the UI. Using logistic regression methods, we analyzed potential predictive factors for UI.
A total of 206 breast cancer patients were included in this study. A total of 120 (58.2%) patients were receiving tamoxifen plus LHRHa, 40 (19.4%) patients were receiving aromatase inhibitor plus LHRHa, and 46 (22.3%) patients were receiving tamoxifen only. In this study, the prevalence of urinary incontinence was found to be 35.9% (n:74). 41% of the patients receiving tamoxifen and 15.0% of those receiving aromatase inhibitors had complaints of urinary incontinence. There was a statistically significant difference between patients receiving tamoxifen or aromatase inhibitor in terms of urinary incontinence (p=0.001). In the univariate analysis established to predict UI, parity (≥2 vs <2) (OR = 3.23, 95% CI: 1.62-6.46, p= 0.001), tamoxifen (vs AI) (OR = 3.97, 95% CI: 1.58-9.98, p= 0.003), age ( ≥40 vs. <40) (OR = 2.80, 95% CI: 1.37-5.71, p= 0.005), vaginal deliveries (≥2 vs. <2) (OR = 3.28, 95% CI: 1.44-7.46, p= 0.005), hypertension (OR = 3.59, 95% CI: 1.43-9.02, p= 0.007), diuretic use (OR = 2.55, 95% CI: 1.09-5.95, p= 0.031) ), and body mass index (≥25 vs <25) (OR = 1.94, 95% CI: 1.05-3.63), p= 0.034) was found to be predictive. Tamoxifen (OR = 4.71, 95% CI: 1.77-12.56, p= 0.002), hypertension (OR = 3.48, 95% CI: 1.27-9.52, p= 0.015), and age (OR = 2.35, 95% CI: 1.10-5.02, p= 0.027) remained independent predictors for incontinence in multivariate analyses.
We found that tamoxifen had increased the risk of urinary incontinence compared to aromatase inhibitors in patients receiving hormone therapy for breast cancer. In addition, we showed that age and hypertension were also independent predictors for UI. In the context of quality of life, we recommend close follow-up of these patients, as drug adherence may be affected in the event of urinary incontinence.
本研究的主要目的是比较绝经前女性接受乳腺癌辅助激素治疗时,他莫昔芬与芳香化酶抑制剂(AI)在尿失禁(UI)方面的差异。次要目的是调查 UI 的患病率和影响因素。
本研究设计为多中心、横断面研究,纳入了 2021 年 6 月至 2022 年 9 月期间≤50 岁、接受他莫昔芬(联合/不联合 LHRHa)或 AI(联合 LHRHa)至少 6 个月的绝经前乳腺癌患者。排除了激素治疗前有尿失禁和转移性患者。使用国际尿失禁咨询问卷尿失禁模块简表(ICIQ UI-SF)的土耳其验证版来确定 UI。我们使用逻辑回归方法分析了 UI 的潜在预测因素。
本研究共纳入 206 例乳腺癌患者。共有 120 例(58.2%)患者接受他莫昔芬加 LHRHa,40 例(19.4%)患者接受 AI 加 LHRHa,46 例(22.3%)患者接受他莫昔芬单药治疗。本研究中,尿失禁的患病率为 35.9%(n:74)。接受他莫昔芬和 AI 的患者中,分别有 41%和 15.0%有尿失禁症状。在接受他莫昔芬或 AI 的患者中,尿失禁的发生率存在统计学显著差异(p=0.001)。在建立的预测 UI 的单因素分析中,产次(≥2 次与<2 次)(OR=3.23,95%CI:1.62-6.46,p=0.001)、他莫昔芬(与 AI)(OR=3.97,95%CI:1.58-9.98,p=0.003)、年龄(≥40 岁与<40 岁)(OR=2.80,95%CI:1.37-5.71,p=0.005)、阴道分娩次数(≥2 次与<2 次)(OR=3.28,95%CI:1.44-7.46,p=0.005)、高血压(OR=3.59,95%CI:1.43-9.02,p=0.007)、利尿剂使用(OR=2.55,95%CI:1.09-5.95,p=0.031)和体重指数(≥25 与<25)(OR=1.94,95%CI:1.05-3.63,p=0.034)与 UI 相关。在多因素分析中,他莫昔芬(OR=4.71,95%CI:1.77-12.56,p=0.002)、高血压(OR=3.48,95%CI:1.27-9.52,p=0.015)和年龄(OR=2.35,95%CI:1.10-5.02,p=0.027)仍然是 UI 的独立预测因素。
我们发现,与接受乳腺癌辅助激素治疗的患者相比,他莫昔芬增加了尿失禁的风险。此外,我们还表明,年龄和高血压也是 UI 的独立预测因素。在生活质量方面,我们建议密切关注这些患者,因为如果发生尿失禁,可能会影响药物依从性。