Hepatocellular Carcinoma Clinical Trial
Official title:
A Novel Immunotherapy PD-1 Antiboty to Suppress Recurrence of Hepatocellular Carcinoma Combined With Portal Vein Thrombus After Hepatic Resection
Hepatic resection is the most effective curative treatment for resectable HCC, whereas
frequent recurrence usually impaired the efficacy of hepatic resection and contributed poor
survivals. PVTT has been certified as an independent risk of early recurrence.
Although TACE has been used to decrease the intraheptic recurrence. However, the intraheptic
recurrence rate remains high and meanwhile it is uncapable to suppress extrahepatic
recurrence. In addition, systematic therapy the small molecular target antiangiogenesis
medicine sorafenib were used to prevent recurrence. Unfortunately, the STORM trial shows that
postoperative antiangiogenesis therapy was failed to suppress recurrence and prolong survival
period for HCC patients. Thus, novel effective systematic therapy to suppress postoperative
recurrence is in urgent need.
At present, the PD-1 antibody has presented a promising and safe therapeutic result of
unresectable HCC and provided good survival benefit for advanced HCC patients. Consistent
with this, we proposed a hypothesis that a novel immunetherapy using the PD-1 antibody could
suppress postoperative recurrence and prolong HCC patients survival period effectively.
Hepatic resection is the most effective curative treatment for resectable hepatocellular
carcinoma (HCC), whereas frequent recurrence usually impaired the efficacy of hepatic
resection and contributed poor survivals. Portal vein tumor thrombus (PVTT) has been
certified as an independent risk of early recurrence (≤2years after hepatic resection).
Although Transarterial Chemoembolization (TACE) has been used as an effective local adjuvant
treatment to decrease the intraheptic recurrence. However, the intraheptic recurrence rate
remains high and meanwhile it is uncapable to suppress extrahepatic recurrence. In addition,
systematic therapy the small molecular target antiangiogenesis medicine sorafenib were used
to prevent recurrence. Unfortunately, the double blind randomized STORM trial shows a
negative result that postoperative antiangiogenesis therapy was failed to suppress recurrence
and prolong survival period for HCC patients. Thus, novel effective systematic therapy to
suppress postoperative recurrence is in urgent need.
At present, the PD-1 antibody has presented a promising and safe therapeutic result of
unresectable HCC and provided good survival benefit for advanced HCC patients. Consistent
with this, we proposed a hypothesis that a novel immunetherapy using the PD-1 antibody could
suppress postoperative recurrence and prolong HCC patients survival period effectively.
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