Fatigue is a common side effect of interferon (IFN) therapy, reported in 70
-100% of patients treated with IFN. The etiology of IFN-mediated fatigue (I
MF) is multifactorial, with endocrine failure, neuropsychiatric disturbance
, autoimmunity, and cytokine dysregulation potentially being contributors.
Thyroid dysfunction, associated with the development of autoantibodies, is
seen in 8-20% of patients receiving IFN-alpha. IFN-alpha also suppresses th
e hypothalamic-pituitary-adrenal axis. In addition, IFN-alpha therapy leads
to depression and cognitive slowing, and depressed patients are predispose
d to develop fatigue. Clinical management of IMF is challenging because the
syndrome is variable in onset and severity and the pathophysiology is poor
ly understood. Current management typically centers on dose reduction, but
ancillary nonpharmacologic measures may help improve symptoms. Other strate
gies include antidepressant or anxiolytic therapy and treatment of coexisti
ng hypothyroidism. Future studies utilizing IFN showd include quantitative
guidelines for grading and managing IMF. (C) 2001 American Cancer Society.