TY - JOUR
T1 - The biology of cancer-related fatigue
T2 - a review of the literature
AU - Saligan, Leorey N.
AU - Olson, Karin
AU - Filler, Kristin
AU - Larkin, David
AU - Cramp, Fiona
AU - Sriram, Yennu
AU - Escalante, Carmen P.
AU - del Giglio, Auro
AU - Kober, Kord M.
AU - Kamath, Jayesh
AU - Palesh, Oxana
AU - Mustian, Karen
N1 - Funding Information:
This research was supported by the Multinational Association of Supportive Care in Cancer and the Division of Intramural Research, National Institute of Nursing Research, National Institutes of Health, and Grants NCI K07CA120025, UG1 CA189961 and R01 CA181064.
Publisher Copyright:
© 2015, Springer-Verlag Berlin Heidelberg (Outside the USA).
PY - 2015/8/29
Y1 - 2015/8/29
N2 - Purpose: Understanding the etiology of cancer-related fatigue (CRF) is critical to identify targets to develop therapies to reduce CRF burden. The goal of this systematic review was to expand on the initial work by the National Cancer Institute CRF Working Group to understand the state of the science related to the biology of CRF and, specifically, to evaluate studies that examined the relationships between biomarkers and CRF and to develop an etiologic model of CRF to guide researchers on pathways to explore or therapeutic targets to investigate. Methods: This review was completed by the Multinational Association of Supportive Care in Cancer Fatigue Study Group–Biomarker Working Group. The initial search used three terms (biomarkers, fatigue, cancer), which yielded 11,129 articles. After removing duplicates, 9145 articles remained. Titles were assessed for the keywords “cancer” and “fatigue” resulting in 3811 articles. Articles published before 2010 and those with samples <50 were excluded, leaving 75 articles for full-text review. Of the 75 articles, 28 were further excluded for not investigating the associations of biomarkers and CRF. Results: Of the 47 articles reviewed, 25 were cross-sectional and 22 were longitudinal studies. More than half (about 70 %) were published recently (2010–2013). Almost half (45 %) enrolled breast cancer participants. The majority of studies assessed fatigue using self-report questionnaires, and only two studies used clinical parameters to measure fatigue. Conclusions: The findings from this review suggest that CRF is linked to immune/inflammatory, metabolic, neuroendocrine, and genetic biomarkers. We also identified gaps in knowledge and made recommendations for future research.
AB - Purpose: Understanding the etiology of cancer-related fatigue (CRF) is critical to identify targets to develop therapies to reduce CRF burden. The goal of this systematic review was to expand on the initial work by the National Cancer Institute CRF Working Group to understand the state of the science related to the biology of CRF and, specifically, to evaluate studies that examined the relationships between biomarkers and CRF and to develop an etiologic model of CRF to guide researchers on pathways to explore or therapeutic targets to investigate. Methods: This review was completed by the Multinational Association of Supportive Care in Cancer Fatigue Study Group–Biomarker Working Group. The initial search used three terms (biomarkers, fatigue, cancer), which yielded 11,129 articles. After removing duplicates, 9145 articles remained. Titles were assessed for the keywords “cancer” and “fatigue” resulting in 3811 articles. Articles published before 2010 and those with samples <50 were excluded, leaving 75 articles for full-text review. Of the 75 articles, 28 were further excluded for not investigating the associations of biomarkers and CRF. Results: Of the 47 articles reviewed, 25 were cross-sectional and 22 were longitudinal studies. More than half (about 70 %) were published recently (2010–2013). Almost half (45 %) enrolled breast cancer participants. The majority of studies assessed fatigue using self-report questionnaires, and only two studies used clinical parameters to measure fatigue. Conclusions: The findings from this review suggest that CRF is linked to immune/inflammatory, metabolic, neuroendocrine, and genetic biomarkers. We also identified gaps in knowledge and made recommendations for future research.
KW - Cancer-related fatigue
KW - Genetic
KW - Inflammation
KW - Metabolic
KW - Neuroendocrine
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U2 - 10.1007/s00520-015-2763-0
DO - 10.1007/s00520-015-2763-0
M3 - Review article
C2 - 25975676
AN - SCOPUS:84933179314
SN - 0941-4355
VL - 23
SP - 2461
EP - 2478
JO - Supportive Care in Cancer
JF - Supportive Care in Cancer
IS - 8
ER -