Saligan Leorey N, Olson Karin, Filler Kristin, Larkin David, Cramp Fiona, Yennurajalingam Sriram, Escalante Carmen P, del Giglio Auro, Kober Kord M, Kamath Jayesh, Palesh Oxana, Mustian Karen
National Institute of Nursing Research, National Institutes of Health, 9000 Rockville Pike, Building 3, Room 5E14, Bethesda, MD, 20892, USA,
Support Care Cancer. 2015 Aug;23(8):2461-78. doi: 10.1007/s00520-015-2763-0. Epub 2015 May 15.
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.
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.
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.
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.
了解癌症相关疲劳(CRF)的病因对于确定开发减轻CRF负担疗法的靶点至关重要。本系统评价的目的是在国家癌症研究所CRF工作组的初步工作基础上进行拓展,以了解与CRF生物学相关的科学现状,特别是评估研究生物标志物与CRF之间关系的研究,并建立CRF的病因模型,以指导研究人员探索相关途径或研究治疗靶点。
本评价由癌症疲劳研究组-生物标志物工作组的多国支持性癌症护理协会完成。最初的搜索使用了三个术语(生物标志物、疲劳、癌症),共检索到11129篇文章。去除重复项后,剩余9145篇文章。对标题进行“癌症”和“疲劳”关键词评估,得到3811篇文章。排除2010年以前发表的文章和样本量小于50的文章,剩余75篇文章进行全文评审。在这75篇文章中,有28篇因未研究生物标志物与CRF的关联而被进一步排除。
在评审的47篇文章中,25篇为横断面研究,22篇为纵向研究。超过一半(约70%)是最近(2010 - 2013年)发表的。几乎一半(45%)的研究纳入了乳腺癌患者。大多数研究使用自我报告问卷评估疲劳,只有两项研究使用临床参数测量疲劳。
本评价的结果表明,CRF与免疫/炎症、代谢、神经内分泌和遗传生物标志物有关。我们还确定了知识空白,并对未来研究提出了建议。