A randomized placebo-controlled trial of bupropion for Cancer-related fatigue: Study design and procedures

被引:8
|
作者
Jim, Heather S. L. [1 ]
Hoogland, Aasha, I [1 ]
Han, Hyo Sook [1 ]
Culakova, Eva [2 ]
Heckler, Charles [2 ]
Janelsins, Michelle [2 ]
Williams, Geoffrey C. [2 ]
Bower, Julienne [3 ]
Cole, Stephen [3 ]
Desta, Zeruesenay [4 ]
Babilonia, Margarita Bobonis [1 ]
Morrow, Gary [2 ]
Peppone, Luke [2 ]
机构
[1] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL 33612 USA
[2] Univ Rochester, Med Ctr, Rochester, NY 14642 USA
[3] Univ Calif Los Angeles, Los Angeles, CA USA
[4] Indiana Univ Sch Med, Indianapolis, IN 46202 USA
关键词
Fatigue; Bupropion; Breast cancer; Randomized controlled trial; Protocol; QUALITY-OF-LIFE; COGNITIVE-BEHAVIORAL THERAPY; PATIENT-REPORTED OUTCOMES; NECROSIS-FACTOR-ALPHA; BREAST-CANCER; DOUBLE-BLIND; FUNCTIONAL ASSESSMENT; PHYSICAL-ACTIVITY; PROMIS MEASURES; IN-VITRO;
D O I
10.1016/j.cct.2020.105976
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Background: Cancer-related fatigue is a significant problem and is associated with poor quality of life. Behavioral interventions include exercise and cognitive-behavioral therapy, which survivors may be unwilling or unable to adopt. Pharmacologic interventions (e.g., selective serotonin reuptake inhibitors) have been disappointing. One potential therapy is the antidepressant bupropion, a norepinephrine-dopamine reuptake inhibitor that targets both inflammation and the hypothalamic-pituitary-adrenal axis. The current study is intended to provide a rigorous test of the efficacy and tolerability of bupropion for cancer-related fatigue. Methods: A randomized, double-blind, placebo-controlled trial will examine the effects of bupropion on cancer-related fatigue. The trial will be conducted nationwide through the University of Rochester Medical Center (URMC) National Cancer Institute Community Oncology Research Program (NCORP). Disease-free breast cancer survivors (n = 422) who completed chemotherapy and/or radiotherapy 12-60 months previously and report significant fatigue will be randomized 1:1 to receive bupropion (300 mg/day) or placebo. Outcomes will be assessed at baseline and the 12-week follow-up. The primary outcome, fatigue, will be measured with the Functional Assessment of Chronic Illness Therapy - Fatigue (FACIT-F). Secondary outcomes include quality of life, depression, and drug tolerability. Exploratory outcomes include cognition and symptomatology. Potential biological mechanisms and genetic moderators of cancer-related fatigue will also be explored. Discussion: This study is the first placebo-controlled trial to our knowledge to evaluate bupropion for cancer-related fatigue. Positive results could revolutionize the treatment of cancer-related fatigue, as bupropion is safe, inexpensive, widely-available, and may be more tolerable and acceptable for many patients than current, limited treatment options.
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页数:9
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