The degree of readiness of selected biomarkers for the early detection of hepatocellular carcinoma: Notes from a recent workshop

被引:30
作者
Block, Timothy M. [1 ]
Marrero, Jorge [2 ]
Gish, Robert G. [3 ]
Sherman, Morris [4 ]
London, W. Thomas [5 ]
Srivastava, Sudhir [6 ]
Wagner, Paul D. [6 ]
机构
[1] Drexel Univ, Coll Med, Drexel Inst Biotechnol & Virol Res, Doylestown, PA USA
[2] Univ Michigan Hlth Syst, Ann Arbor, MI USA
[3] Calif Pacific Med Ctr, San Francisco, CA USA
[4] Univ Toronto, Toronto, ON M5S 1A1, Canada
[5] Fox Chase Canc Ctr, Philadelphia, PA 19111 USA
[6] NCI, Bethesda, MD 20892 USA
关键词
biomarkers; hepatocellular; carcinoma; fibrosis; cirrhosis;
D O I
10.3233/CBM-2008-4103
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
This opinion piece evaluates the degree of readiness of 13 candidate biomarkers or panels of biomarkers for the early detection of hepatocellular carcinoma (HCC), or for the staging of liver fibrosis. As candidate biomarkers for the early detection of disease are identified, it is important to understand where they are in the developmental pipeline and how they might be employed. HCC is a growing public health problem, and its early detection is believed to be important in its management. Current detection methods are limited in usefulness or practicality, and there is a need for better methods to diagnose liver disease. Therefore, a number of candidate biomarkers, considered to be attractive because of their advanced stage of development or inherent scientific value, were evaluated for specificity and sensitivity for detection of liver disease. Study design, confirmatory evidence and assay practicality associated with each of the biomarkers are considered. The comments in this review reflect the authors' opinions and are based on a recent workshop convened by the Hepatitis B Foundation of America and the US National Cancer Institute's Early Detection Research Network. It is emphasized that only a selected set of biomarkers was considered; thus, this review is not comprehensive and not intended to review all candidate HCC biomarkers.
引用
收藏
页码:19 / 33
页数:15
相关论文
共 60 条
[1]   ALPHA1 FETOGLOBULIN IN DIAGNOSIS OF HUMAN HEPATOMA [J].
ALPERT, ME ;
URIEL, J ;
DENECHAU.B .
NEW ENGLAND JOURNAL OF MEDICINE, 1968, 278 (18) :984-&
[2]   Making sense of latent TGFβ activation [J].
Annes, JP ;
Munger, JS ;
Rifkin, DB .
JOURNAL OF CELL SCIENCE, 2003, 116 (02) :217-224
[3]  
Aoyagi Y, 1998, CANCER, V83, P2076, DOI 10.1002/(SICI)1097-0142(19981115)83:10<2076::AID-CNCR5>3.0.CO
[4]  
2-L
[5]   CARBOHYDRATE-BASED MEASUREMENTS ON ALPHA-FETOPROTEIN IN THE EARLY DIAGNOSIS OF HEPATOCELLULAR-CARCINOMA [J].
AOYAGI, Y .
GLYCOCONJUGATE JOURNAL, 1995, 12 (03) :194-199
[6]   Use of targeted glycoproteomics to identify serum glycoproteins that correlate with liver cancer in woodchucks and humans [J].
Block, TM ;
Comunale, MA ;
Lowman, M ;
Steel, LF ;
Romano, PR ;
Fimmel, C ;
Tennant, BC ;
London, WT ;
Evans, AA ;
Blumberg, BS ;
Dwek, RA ;
Mattu, TS ;
Mehta, AS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2005, 102 (03) :779-784
[7]   Molecular viral oncology of hepatocellular carcinoma [J].
Block, TM ;
Mehta, AS ;
Fimmel, CJ ;
Jordan, R .
ONCOGENE, 2003, 22 (33) :5093-5107
[8]   HEPATITIS-B VIRUS (HBV) AND HEPATOCELLULAR-CARCINOMA - HBV DNA STATUS AND ITS IMPLICATIONS [J].
BRECHOT, C .
JOURNAL OF HEPATOLOGY, 1987, 4 (02) :269-279
[9]   Management of hepatoceullular carcinoma [J].
Bruix, J ;
Sherman, M .
HEPATOLOGY, 2005, 42 (05) :1208-1236
[10]   SERUM-ALPHA-FETOPROTEIN HETEROGENEITY AS A MEANS OF DIFFERENTIATING BETWEEN PRIMARY HEPATOCELLULAR-CARCINOMA AND HEPATIC SECONDARIES [J].
BUAMAH, PK ;
GIBB, I ;
BATES, G ;
WARD, AM .
CLINICA CHIMICA ACTA, 1984, 139 (03) :313-316