Tumor Markers for Hepatocellular Carcinoma: Simple and Significant Predictors of Outcome in Patients with HCC

被引:133
作者
Toyoda, Hidenori [1 ]
Kumada, Takashi [1 ]
Tada, Toshifumi [1 ]
Sone, Yasuhiro [2 ]
Kaneoka, Yuji [3 ]
Maeda, Atsuyuki [3 ]
机构
[1] Ogaki Municipal Hosp, Dept Gastroenterol, 4-86 Minaminokawa, Ogaki, Gifu 5038502, Japan
[2] Ogaki Municipal Hosp, Radiol, Ogaki, Gifu, Japan
[3] Ogaki Municipal Hosp, Surg, Gifu, Japan
关键词
Alpha-fetoprotein; Des-gamma-carboxy prothrombin; Hepatocellular carcinoma; Lens culinaris agglutinin-reactive fraction of alpha-fetoprotein; Prognosis; GAMMA-CARBOXY PROTHROMBIN; REACTIVE ALPHA-FETOPROTEIN; GD-EOB-DTPA; ENZYME-IMMUNOASSAY KIT; HEPATITIS-C; PROGNOSTIC-SIGNIFICANCE; SERUM-LEVELS; ABNORMAL PROTHROMBIN; CLINICAL-EVALUATION; EARLY-DIAGNOSIS;
D O I
10.1159/000367735
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The effectiveness of tumor markers in evaluating outcomes of patients with hepatocellular carcinoma (HCC) remains to be clarified. Summary: The usefulness of the HCC tumor markers, alpha-fetoprotein (AFP), Lens culinaris agglutinin-reactive fraction of alpha-fetoprotein (AFP-L3), and des-gamma-carboxy prothrombin (DCP) was reviewed. Elevations in these tumor markers at the time of HCC diagnosis correlate with disease progression as assessed by both imaging studies and pathologic examinations. The combination of these three tumor markers results in good predictive ability for patient survival after diagnosis. In addition, combination at the time of HCC diagnosis of these three tumor markers (as a measure of tumor progression) and serum albumin and bilirubin levels (as indicators of remnant liver function) can be used for HCC staging and further predicts prognosis in patients with HCC. Key Message: The prognosis of patients with HCC can be well discriminated based solely on serum markers. Staging of HCC with serum markers is objective; if stored serum samples are available, HCC stages can be standardized across different countries and time periods. Copyright (C) 2015 S. Karger AG, Basel
引用
收藏
页码:126 / 136
页数:11
相关论文
共 72 条
[1]  
[Anonymous], TNM CLASS MAL TUM
[2]  
[Anonymous], 2003, General Rules for the Clinical and Pathological Study ofPrimary Liver Cancer, V2nd
[3]   Management of Hepatocellular Carcinoma: An Update [J].
Bruix, Jordi ;
Sherman, Morris .
HEPATOLOGY, 2011, 53 (03) :1020-1022
[4]   Glypican-3: A novel serum and histochemical marker for hepatocellular carcinoma [J].
Capurro, M ;
Wanless, IR ;
Sherman, M ;
Deboer, G ;
Shi, W ;
Miyoshi, E ;
Filmus, J .
GASTROENTEROLOGY, 2003, 125 (01) :89-97
[5]   A new prognostic classification for predicting survival in patients with hepatocellular carcinoma [J].
Chevret, S ;
Trinchet, JC ;
Mathieu, D ;
Rached, AA ;
Beaugrand, M ;
Chastang, C .
JOURNAL OF HEPATOLOGY, 1999, 31 (01) :133-141
[6]   Serum alpha-fetoprotein levels in patients with advanced hepatitis C: Results from the HALT-C Trial [J].
Di Bisceglie, AM ;
Sterling, RK ;
Chung, RT ;
Everhart, JE ;
Dienstag, JL ;
Bonkovsky, HL ;
Wright, EC ;
Everson, GT ;
Lindsay, KL ;
Lok, ASF ;
Lee, WM ;
Morgan, TR ;
Ghany, MG ;
Gretch, DR .
JOURNAL OF HEPATOLOGY, 2005, 43 (03) :434-441
[7]   Hepatocellular carcinoma in cirrhotic patients: prospective comparison of US, CT and MR imaging [J].
Di Martino, Michele ;
De Filippis, Gianmaria ;
De Santis, Adriano ;
Geiger, Daniel ;
Del Monte, Maurizio ;
Lombardo, Concetta Valentina ;
Rossi, Massimo ;
Corradini, Stefano Ginanni ;
Mennini, Gianluca ;
Catalano, Carlo .
EUROPEAN RADIOLOGY, 2013, 23 (04) :887-896
[8]  
European Assoc Study Liver, 2012, EUR J CANCER, V48, P599, DOI [10.1016/j.ejca.2011.12.021, 10.1016/j.jhep.2011.12.001]
[9]   Biomarker-based prognosis in hepatocellular carcinoma: validation and extension of the BALAD model [J].
Fox, R. ;
Berhane, S. ;
Teng, M. ;
Cox, T. ;
Tada, T. ;
Toyoda, H. ;
Kumada, T. ;
Kagebayashi, C. ;
Satomura, S. ;
Johnson, P. J. .
BRITISH JOURNAL OF CANCER, 2014, 110 (08) :2090-2098
[10]   Tumor markers in early diagnosis, follow-up and management of patients with hepatocellular carcinoma [J].
Fujiyama, S ;
Tanaka, M ;
Maeda, S ;
Ashihara, H ;
Hirata, R ;
Tomita, K .
ONCOLOGY, 2002, 62 :57-63