Fatigue After Breast Cancer Treatment: Biobehavioral Predictors of Fatigue Trajectories

被引:104
作者
Bower, Julienne E. [1 ,2 ,3 ,4 ]
Wiley, Joshua [5 ]
Petersen, Laura [4 ]
Irwin, Michael R. [1 ,2 ,3 ]
Cole, Steve W. [2 ,3 ,6 ]
Ganz, Patricia A. [4 ,7 ,8 ]
机构
[1] Univ Calif Los Angeles, Dept Psychol, 1285 Franz Hall, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Cousins Ctr Psychoneuroimmunol, Semel Inst, Los Angeles, CA 90095 USA
[3] Univ Calif Los Angeles, Dept Psychiat & Biobehav Sci, Los Angeles, CA 90095 USA
[4] Univ Calif Los Angeles, Jonsson Comprehens Canc Ctr, Div Canc Prevent & Control Res, Los Angeles, CA 90095 USA
[5] Monash Univ, Clayton, Vic, Australia
[6] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90095 USA
[7] UCLA, Sch Med, Los Angeles, CA 90024 USA
[8] UCLA, Sch Publ Hlth, Los Angeles, CA 90024 USA
基金
美国国家卫生研究院;
关键词
fatigue; cancer trajectory; biobehavioral; risk factor; DEPRESSIVE SYMPTOM TRAJECTORIES; CHILDHOOD ADVERSITY; ADJUVANT CHEMOTHERAPY; BEHAVIORAL SYMPTOMS; PROSPECTIVE COHORT; RADIATION-THERAPY; RISK-FACTORS; WOMEN; STRESS; SURVIVORS;
D O I
10.1037/hea0000652
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: Fatigue is a common side effect of cancer treatment, but there is considerable variability in fatigue severity and persistence among survivors. This study aimed to characterize longitudinal trajectories of fatigue after breast cancer treatment and to identify predictors of varying fatigue trajectories. Methods: Women (N = 191) from the Mind-Body Study completed assessments after primary treatment for early stage breast cancer and at regular follow-ups that occurred up to 6 years after treatment (M = 4.3 years). Growth mixture models were used to characterize fatigue trajectories, and demographic, medical, and biobehavioral risk factors were examined as predictors of trajectory group. Results: Five trajectories were identified, characterized as High, Recovery, Late, Low, and Very Low fatigue. The High and Recovery groups (40% of sample) evidenced elevated fatigue at posttreatment that declined in Recovery but persisted in the High group. In bivariate analyses, trajectory groups differed significantly on depressive symptoms, sleep disturbance, childhood adversity, body mass index, and the inflammatory marker soluble TNF receptor type II, which were higher in the High and/or Recovery groups. In multivariate models, depressive symptoms and childhood adversity distinguished High and Recovery from other groups. Rates of chemotherapy were higher in the Recovery than in the High or Late group, whereas rates of endocrine therapy were higher in the High than in the Recovery group. Conclusions: There are distinct longitudinal trajectories of fatigue after breast cancer treatment. Psychological factors are strongly associated with adverse fatigue trajectories, and together with treatment exposures may increase risk for cancer-related fatigue.
引用
收藏
页码:1025 / 1034
页数:10
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