A concordance of multiple advances is changing the management of
hepatocellular carcinoma (HCC). These include: (1) identification of preventable and treatable causal factors, including
hepatitis B and
obesity (non-alcoholic steatotic
hepatitis [NASH]); (2) description of molecular and proteomic profiles for HCC prognosis, disease subtyping, and
drug selection; (3) identification of
circulating tumor cells for non-invasive molecular typing; (4) identification of tumor stem cells, for HCC subtyping and as treatment targets; (5) large numbers of multi-
kinase inhibitors that are currently undergoing clinical trial assessment and comparison; (6) an array of newer
therapies of different
drug classes, aimed at a wide range of targets in cell growth, apoptosis, autophagy, and
tumor invasion pathways; (7) newer regional
chemotherapy and
radiotherapy regimens and delivery systems; (8) the extension of
liver transplantation to larger HCCs and its wider availability through use of living-related organ donors; (9) new radiological techniques to assess the changes in HCC vascularity associated with angiogenic
drug actions; (10) re-evaluation of the importance of
tumor biopsy to obtain molecular signatures; (11) recognition of the importance of non-
tumor liver parenchyma for
tumor growth control and as a source of prognostic profiling in HCC patients; (12) the evaluation of
kinase- and other inhibitors in neo-adjuvant and adjuvant
therapy associated with resection and
liver transplant and minimization of transplant waiting list drop-out; (13) re-evaluation of the role or limitation of
tumor responses, since
kinase inhibitors can enhance survival without HCC size responses; and (14) the development of combination
therapies to enhance
tumor control rates, either using drugs targeting differing pathways, or
kinase-inhibitors combined with either
chemotherapy drugs or
yttrium 90.