University of California Davis School of Medicine, Davis, USA.
Department of Public Health Sciences, University of California Davis, One Shields Ave., Med Sci 1C, Davis, CA, 95616, USA.
Breast Cancer Res Treat. 2022 Jan;191(1):125-135. doi: 10.1007/s10549-021-06425-y. Epub 2021 Oct 25.
We compared trajectories of vasomotor symptoms (VMS) and their risk factors in women with breast cancer (BrCa) to those of cancer-free controls.
Data were from 15 nearly annual follow-up visits (1996-2017) of the multi-racial/ethnic cohort of midlife women enrolled in the Study of Women's Health Across the Nation (SWAN). We compared women with incident BrCa to controls for patterns of VMS, controlling for risk factors identified in bivariate analyses using multivariable longitudinal analyses.
Characteristics at study entry largely did not differ between cases (n = 151) and controls (n = 2161). Adjusted prevalence of any VMS increased significantly among cases from diagnosis to 2.75 years post diagnosis [per-year adjusted odds ratio (aOR) = 1.76, 95% confidence interval (CI) 1.39-2.24], peaking at 2.75 years post diagnosis, whereas prevalence was stable among controls in this interval [aOR = 1.04, 95% CI 0.99-1.11]. Beyond 2.75 years post diagnosis, prevalence declined significantly in cases [aOR = 0.72, 95% CI 0.61-0.84] and less in controls [aOR = 0.96, 95% CI 0.92-1.00]. Patterns were similar for frequent VMS. Adjustment for tamoxifen use slightly reduced the per-year OR for any prevalent VMS post diagnosis, partially explaining excess VMS in cases. Other treatments were unassociated with VMS.
Patterns of prevalent VMS reporting differed significantly between cases and controls, particularly post diagnosis, the latter only partially explained by tamoxifen use among cases. Risk factors for VMS largely did not differ between cases and controls.
我们比较了乳腺癌(BrCa)女性与无癌对照者的血管舒缩症状(VMS)轨迹及其危险因素。
数据来自参加全国妇女健康研究(SWAN)的中年多民族/族裔队列的 15 次几乎每年一次的随访(1996-2017 年)。我们将新诊断的 BrCa 女性与对照者进行了 VMS 模式比较,并使用多变量纵向分析控制了双变量分析中确定的危险因素。
病例组(n=151)和对照组(n=2161)在研究开始时的特征基本没有差异。从诊断到诊断后 2.75 年,病例组任何 VMS 的调整后患病率显著增加[每年调整后的优势比(aOR)=1.76,95%置信区间(CI)1.39-2.24],在诊断后 2.75 年达到峰值,而在这段时间内,对照组的患病率保持稳定[aOR=1.04,95%CI 0.99-1.11]。在诊断后 2.75 年以后,病例组的患病率显著下降[aOR=0.72,95%CI 0.61-0.84],对照组下降较少[aOR=0.96,95%CI 0.92-1.00]。频繁 VMS 的模式也相似。调整他莫昔芬的使用后,诊断后任何 VMS 的每年 aOR 略有降低,部分解释了病例组 VMS 的增加。其他治疗方法与 VMS 无关。
病例组和对照组之间报告的 VMS 流行模式差异显著,特别是在诊断后,而病例组仅部分解释为他莫昔芬的使用。VMS 的危险因素在病例组和对照组之间基本没有差异。