Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, MI.
Department of Biostatistics, University of Michigan School of Public Health, Ann Arbor, MI.
Clin Breast Cancer. 2018 Apr;18(2):168-174.e2. doi: 10.1016/j.clbc.2017.12.012. Epub 2017 Dec 27.
Adherence to aromatase inhibitor (AI) therapy is poor, often because of treatment-emergent side effects, including musculoskeletal symptoms, fatigue, and insomnia. In the present analysis, we examined the sleep patterns and daytime function both objectively using actigraphy and subjectively using validated questionnaires in women initiating AI therapy.
Postmenopausal women with stage 0-III hormone receptor-positive breast cancer who were initiating AI therapy were eligible. The patients wore actigraphy devices for 10 consecutive days and completed questionnaires at baseline before the initiation of AI and after 3 months of AI therapy. Associations between the baseline demographics and symptoms, changes in patient-reported outcomes and actigraphy measures from baseline to 3 months of AI therapy and discontinuation of AI therapy were examined using sign tests, logistic regression models, Spearman's correlation, and linear mixed models.
Forty-two patients (86%) completed the baseline assessments and 23 patients (47%) completed both the baseline and the 3-month assessments. Objectively measured daytime function as measured by total daytime activity decreased during the 3 months after starting AI (232,566 activity count vs. 204,205 activity count; P = .023), and the decrease was more evident in women with higher baseline physical function. Reduced daytime activity correlated with increased fatigue (ρ = -0.49; P = .017).
Daytime function decreased after initiation of AI therapy and correlated moderately with increased fatigue, although no association was identified with changes in pain or sleep quality. Additional studies are required to understand why function is reduced, which could have implications for interventions to improve patient tolerance of, and persistence with, AI therapy.
芳香化酶抑制剂(AI)治疗的依从性较差,通常是因为治疗中出现的副作用,包括肌肉骨骼症状、疲劳和失眠。在本分析中,我们使用活动记录仪客观地检查了睡眠模式和白天的功能,并用经过验证的问卷主观地检查了开始 AI 治疗的女性。
有资格参加的是接受 0-III 期激素受体阳性乳腺癌治疗的绝经后妇女,开始 AI 治疗。患者佩戴活动记录仪连续 10 天,并在开始 AI 治疗前和 AI 治疗 3 个月后完成问卷。使用符号检验、逻辑回归模型、Spearman 相关和线性混合模型检查基线人口统计学和症状与患者报告的结果和从基线到 AI 治疗 3 个月期间活动记录仪测量值的变化之间的关联,以及 AI 治疗的停药。
42 名患者(86%)完成了基线评估,23 名患者(47%)完成了基线和 3 个月的评估。白天功能的客观测量值(总白天活动量)在开始 AI 后的 3 个月内下降(232566 个活动计数比 204205 个活动计数;P=0.023),基线身体功能较高的女性下降更为明显。白天活动量减少与疲劳增加相关(ρ=-0.49;P=0.017)。
开始 AI 治疗后白天功能下降,与疲劳增加中度相关,尽管与疼痛或睡眠质量的变化无关。需要进一步的研究来了解为什么功能会下降,这可能对改善患者对 AI 治疗的耐受性和坚持性的干预措施有影响。