TY - JOUR
T1 - Systemic treatment of advanced hepatocellular carcinoma
T2 - From disillusions to new horizons
AU - Hollebecque, Antoine
AU - Malka, David
AU - Ferté, Charles
AU - Ducreux, Michel
AU - Boige, Valérie
N1 - Publisher Copyright:
© 2014 Elsevier Ltd. All rights reserved.
PY - 2015/1/1
Y1 - 2015/1/1
N2 - Hepatocellular carcinoma (HCC) is an aggressive malignancy, which accounts for a third of all cancer deaths globally each year. The management of patients with HCC is complex, as both the tumour stage and any underlying liver disease must be considered conjointly. Since the approval of sorafenib in advanced HCC, several phase III clinical trials have failed to demonstrate any superiority over sorafenib in the frontline setting, and no agent has been shown to impact outcomes after sorafenib failure. This review will focus on the range of experimental therapeutics for patients with advanced HCC and highlight the successes and failures of these treatments as well as areas for future development. Specifics such as dose limiting toxicity and safety profile in patients with liver dysfunction related to the underlying chronic liver disease should be considered when developing therapies in HCC. Finally, robust validated and reproducible surrogate end-points as well as predictive biomarkers should be defined in future randomised trials.
AB - Hepatocellular carcinoma (HCC) is an aggressive malignancy, which accounts for a third of all cancer deaths globally each year. The management of patients with HCC is complex, as both the tumour stage and any underlying liver disease must be considered conjointly. Since the approval of sorafenib in advanced HCC, several phase III clinical trials have failed to demonstrate any superiority over sorafenib in the frontline setting, and no agent has been shown to impact outcomes after sorafenib failure. This review will focus on the range of experimental therapeutics for patients with advanced HCC and highlight the successes and failures of these treatments as well as areas for future development. Specifics such as dose limiting toxicity and safety profile in patients with liver dysfunction related to the underlying chronic liver disease should be considered when developing therapies in HCC. Finally, robust validated and reproducible surrogate end-points as well as predictive biomarkers should be defined in future randomised trials.
KW - Drug development
KW - Hepatocellular carcinoma
KW - Molecular biomarkers
KW - Molecular targeted agents
KW - Signalling pathway
KW - Sorafenib
KW - Systemic treatment
UR - http://www.scopus.com/inward/record.url?scp=84922681438&partnerID=8YFLogxK
U2 - 10.1016/j.ejca.2014.12.005
DO - 10.1016/j.ejca.2014.12.005
M3 - Article
C2 - 25559615
AN - SCOPUS:84922681438
SN - 0959-8049
VL - 51
SP - 327
EP - 339
JO - European Journal of Cancer
JF - European Journal of Cancer
IS - 3
ER -