Copyright
©The Author(s) 2015.
World J Gastroenterol. Jul 28, 2015; 21(28): 8478-8491
Published online Jul 28, 2015. doi: 10.3748/wjg.v21.i28.8478
Published online Jul 28, 2015. doi: 10.3748/wjg.v21.i28.8478
System | Description | When used |
Milan Criteria[4], 1996 | Single tumor ≤ 5 cm, or 2-3 tumors ≤ 3 cm, and no vascular invasion and/or extrahepatic spread. | Staging HCC |
UCSF Criteria[5], 2001 | Single tumor ≤ 6.5 cm, or 2-3 lesions, none exceeding 4.5 cm, with total tumor diameter ≤ 8 cm, no vascular invasion and/or extrahepatic spread. | Staging HCC |
Model for End-Stage Liver Disease Score (MELD)[107], 2000 | Specific equation looking at the variables of bilirubin, INR and serum creatinine. | Transplant prioritization, End-stage liver disease severity by estimating 3 mo mortality |
Barcelona Clinic Liver Cancer (BCLC) Staging[108], 1999 | Variables include tumor stage, liver functional status, physical status, and cancer-related symptoms | Widely accepted treatment algorithm of HCC |
Child-Pugh-Turcott[109,110], 1964-1972 | Variables include bilirubin, albumin, INR, Ascites and presence of encephalopathy | Prognosis/severity of liver disease including cirrhosis |
Tumor-Node-Metastasis[111], 1997 | Variables include the classic tumor size/location, lymph node positivity, and presence of metastasis. | Standard and poorly predictive staging system not currently in use |
Okuda[112], 1985 | Variables include albumin, ascites, bilirubin, and tumor stage (more or less than 50% of liver area involved) | Properly stratified patients with advanced/symptomatic stage and is useful to identify end-stage patients. Lacks early stage predictive capacity |
Japan Integrated Staging (JIS)[113], 2000 | Combines TMN with Child-Pugh | Prognostic staging system for hepatocellular carcinoma |
Drug name | Method of action | Clinical phase |
Lenvatinib | VEGFR, PDGFR, FGFR, RET and c-Kit inhibitor | III, ongoing as 1st line |
Brivanib | VEGFR2 and FGFR tyrosine kinases | III, negative as 1st line |
Everolimus | mTOR inhibitor | III, negative |
Tivantinib | c-MET inhibitor | III, ongoing as 2nd line |
Linifanib | RTK, VEGF and PDGF inhibitor | III, negative as 1st line |
Sorafenib (as adjuvant) | Raf/MEK/ERK inhibitor | III, negative |
Ramucirumab | VEGFR2 | II and III, negative |
Foretinib | c-MET inhibitor | II |
Refametinib | MEK1/2 inhibitor | II |
Mapatumumab | TRAIL-receptor (death receptor 4) | II |
Selumetinib | MAPK/ERK inhibitor | II |
Erlotinib | EGFR tyrosine kinase inhibitor | II |
Lapatinib | EGFR and HER2/neu inhibitor | II |
Cabozantinib | VEGFR2, c-MET, RET, KIT, FLT4, AXL | III |
MSC2156119J | c-MET/HGF | Ib/II |
Lenalidomide | Immunomodulatory | II |
- Citation: Schlachterman A, Jr WWC, Hilgenfeldt E, Mitra A, Cabrera R. Current and future treatments for hepatocellular carcinoma. World J Gastroenterol 2015; 21(28): 8478-8491
- URL: https://www.wjgnet.com/1007-9327/full/v21/i28/8478.htm
- DOI: https://dx.doi.org/10.3748/wjg.v21.i28.8478