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The Doylestown Algorithm: A Test to Improve the Performance of AFP in the Detection of Hepatocellular Carcinoma
Journal article   Open access   Peer reviewed

The Doylestown Algorithm: A Test to Improve the Performance of AFP in the Detection of Hepatocellular Carcinoma

Mengjun Wang, Karthik Devarajan, Amit G Singal, Jorge A Marrero, Jianliang Dai, Ziding Feng, Jo Ann S Rinaudo, Sudhir Srivastava, Alison Evans, Hie-Won Hann, …
Cancer prevention research (Philadelphia, Pa.), v 9(2), pp 172-179
Feb 2016
PMID: 26712941
url
https://europepmc.org/articles/pmc4740237View
Accepted (AM)Open Access (License Unspecified) Open
url
https://doi.org/10.1158/1940-6207.CAPR-15-0186View
Published, Version of Record (VoR) Open

Abstract

Algorithms alpha-Fetoproteins - analysis Biomarkers, Tumor - blood Carcinoma, Hepatocellular - blood Carcinoma, Hepatocellular - diagnosis Case-Control Studies Cohort Studies Follow-Up Studies Humans Immunoenzyme Techniques Liver Cirrhosis - blood Liver Cirrhosis - diagnosis Liver Neoplasms - blood Liver Neoplasms - diagnosis Logistic Models Neoplasm Staging Prognosis ROC Curve
Biomarkers for the early diagnosis of hepatocellular carcinoma (HCC) are needed to decrease mortality from this cancer. However, as new biomarkers have been slow to be brought to clinical practice, we have developed a diagnostic algorithm that utilizes commonly used clinical measurements in those at risk of developing HCC. Briefly, as α-fetoprotein (AFP) is routinely used, an algorithm that incorporated AFP values along with four other clinical factors was developed. Discovery analysis was performed on electronic data from patients who had liver disease (cirrhosis) alone or HCC in the background of cirrhosis. The discovery set consisted of 360 patients from two independent locations. A logistic regression algorithm was developed that incorporated log-transformed AFP values with age, gender, alkaline phosphatase, and alanine aminotransferase levels. We define this as the Doylestown algorithm. In the discovery set, the Doylestown algorithm improved the overall performance of AFP by 10%. In subsequent external validation in over 2,700 patients from three independent sites, the Doylestown algorithm improved detection of HCC as compared with AFP alone by 4% to 20%. In addition, at a fixed specificity of 95%, the Doylestown algorithm improved the detection of HCC as compared with AFP alone by 2% to 20%. In conclusion, the Doylestown algorithm consolidates clinical laboratory values, with age and gender, which are each individually associated with HCC risk, into a single value that can be used for HCC risk assessment. As such, it should be applicable and useful to the medical community that manages those at risk for developing HCC.

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Collaboration types
Domestic collaboration
Web of Science research areas
Oncology
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