4.7 Article

Does tumor necrosis factor-alpha (TNF-α) play a role in post-chemotherapy cerebral dysfunction?

Journal

BRAIN BEHAVIOR AND IMMUNITY
Volume 30, Issue -, Pages S99-S108

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.bbi.2012.07.015

Keywords

Breast cancer; Cognitive complaints; Chemotherapy; Proinflammatory cytokines; TNF-alpha; Neuropsychological testing; Brain imaging

Funding

  1. Breast Cancer Research Foundation (BCRF) [NIH/NCI R01 CA 109650]
  2. an American Society Clinical Research Professorship
  3. UCLA Older Americans Independence Center (OAIC)
  4. OAIC Inflammatory Biology Core [NIH/NIA P30-AG028748]
  5. Norman Cousins Center [PNI. R01-AG034588, R01-AG026364, R01-CA119159, R01-HL079955, R01-HL095799, P30-AG028748, UL RR 033176]

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Post-chemotherapy treated cancer patients frequently report cognitive difficulties. The biology of this phenomenon is poorly understood, with uncertainty about possible direct toxic effects on the brain, secondary effects from systemic inflammation, host factors/genetic predisposition to cognitive complaints, or hormonal changes influencing cognitive function. To elucidate possible mechanisms associated with post-treatment cognitive dysfunction among breast cancer survivors, in 2007 we established a prospective, longitudinal, observational cohort study of early stage breast cancer patients, recruited at the end of initial treatments (primary treatment exposure included surgery, +/- radiation, +/- chemotherapy), and prior to the initiation of adjuvant endocrine therapy. We assessed cognitive complaints, neuropsychological (NP) test performance, markers of inflammation, and brain imaging at baseline, 6 months and 12 months after enrollment. In this analysis of data from the first 93 patients enrolled in the cohort study, we focus on the relationship of circulating levels of proinflammatory cytokines to cerebral functioning and chemotherapy exposure. Among the proinflammatory cytokines tested (IL-1ra, sTNE-RII, CRP, and IL-6) at baseline, only sTNE-RII was increased among chemotherapy exposed patients, with a significant decline in the year after treatment (p = 0.003). Higher baseline sTNE-RII in chemotherapy patients was significantly associated with increased memory complaints. In chemotherapy exposed patients, the longitudinal decline in sTNE-RII was significantly correlated with fewer memory complaints over 12 months (r = -0.34, p = 0.04). Higher baseline sTNE-RII was also associated with relatively diminished brain metabolism in the inferior frontal cortex (r = -0.55, p = 0.02), as well as relatively increased inferior frontal metabolism after 1 year, in chemotherapy-exposed subjects. These preliminary findings suggest that post-chemotherapy increases in TNF-alpha, may be playing an important role in the manifestations of cognitive complaints in breast cancer survivors. (C) 2012 Elsevier Inc. All rights reserved.

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