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

Contemp Clin Trials. 2020 Apr:91:105976. doi: 10.1016/j.cct.2020.105976. Epub 2020 Mar 5.

Abstract

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.

Keywords: Breast cancer; Bupropion; Fatigue; Protocol; Randomized controlled trial.

Publication types

  • Clinical Trial Protocol
  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Age Factors
  • Antidepressive Agents, Second-Generation / administration & dosage
  • Antidepressive Agents, Second-Generation / adverse effects
  • Antidepressive Agents, Second-Generation / pharmacokinetics
  • Antidepressive Agents, Second-Generation / therapeutic use*
  • Breast Neoplasms / complications*
  • Bupropion / administration & dosage
  • Bupropion / adverse effects
  • Bupropion / pharmacokinetics
  • Bupropion / therapeutic use*
  • Cancer Survivors*
  • Cytochrome P-450 CYP2B6 / genetics
  • Delayed-Action Preparations
  • Depression / etiology
  • Double-Blind Method
  • Fatigue / drug therapy*
  • Fatigue / etiology*
  • Fatigue / genetics
  • Female
  • Health Behavior
  • Humans
  • Menopause
  • Quality of Life
  • Randomized Controlled Trials as Topic
  • Research Design
  • Socioeconomic Factors
  • Vinca Alkaloids

Substances

  • Antidepressive Agents, Second-Generation
  • Delayed-Action Preparations
  • Vinca Alkaloids
  • Bupropion
  • 2-(nitrooxy)ethyl apovincaminate
  • CYP2B6 protein, human
  • Cytochrome P-450 CYP2B6