Progress with Metabolomic Blood Tests for Gastrointestinal Cancer Diagnosis—An Assessment of Biomarker Translation

生物标志物 医学 癌症 结直肠癌 生物标志物发现 胃肠道癌 转化研究 内科学 肿瘤科 生物信息学 病理 蛋白质组学 生物 生物化学 基因 化学
作者
Katerina-Vanessa Savva,Bibek Das,Stefan Antonowicz,George B. Hanna,Christopher J. Peters
出处
期刊:Cancer Epidemiology, Biomarkers & Prevention [American Association for Cancer Research]
卷期号:31 (12): 2095-2105 被引量:13
标识
DOI:10.1158/1055-9965.epi-22-0307
摘要

Abstract There is an urgent need for cost-effective, non-invasive tools to detect early stages of gastrointestinal cancer (colorectal, gastric, and esophageal cancers). Despite many publications suggesting circulating metabolites acting as accurate cancer biomarkers, few have reached the clinic. In upper gastrointestinal cancer this is critically important, as there is no test to complement gold-standard endoscopic evaluation in patients with mild symptoms that do not meet referral criteria. Therefore, this study aimed to describe and solve this translational gap. Studies reporting diagnostic accuracy of metabolomic blood-based gastrointestinal cancer biomarkers from 2007 to 2020 were systematically reviewed and progress of each biomarker along the discovery–validation–adoption pathway was mapped. Successful biomarker translation was defined as a composite endpoint, including patent protection/FDA approval/recommendation in national guidelines. The review found 77 biomarker panels of gastrointestinal cancer, including 25 with an AUROC >0.9. All but one was stalled at the discovery phase, 9.09% were patented and none were clinically approved, confirming the extent of biomarker translational gap. In addition, there were numerous “re-discoveries,” including histidine, discovered in 7 colorectal studies. Finally, this study quantitatively supports the presence of a translational gap between discovery and clinical adoption, despite clear evidence of highly performing biomarkers with significant potential clinical value.
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