Complete regression of locally advanced hepatocellular carcinoma induced by sorafenib allowing curative resection

Liver Int. 2011 May;31(5):740-3. doi: 10.1111/j.1478-3231.2010.02441.x. Epub 2011 Jan 11.

Abstract

We report two cases of locally advanced hepatocellular carcinoma (HCC) with portal vein tumour thrombosis (PVTT) who complete regression by sorafenib treatment allowed curative resection. Two male adult (59 and 57 years) cirrhotic patients with HCC associated with PVTT including one with lymph node involvement had elevated α-fetoprotein level (AFP) (867 and 17 000) and were treated with standard sorafenib treatment during 10 and 12 months respectively. Size decrease of the main tumour, disappearance of PVTT and normalization of AFP allowed curative surgical resection. No viable tumour cells were found in the specimen and the two patients are currently alive without recurrence 12 and 16 months after surgery. These first two cases of complete tumour necrosis after sorafenib treatment allow us to reconsider surgical treatment in patients with unresectable HCC responding to this medical treatment.

Publication types

  • Case Reports

MeSH terms

  • Antineoplastic Agents / administration & dosage*
  • Benzenesulfonates / administration & dosage*
  • Carcinoma, Hepatocellular / drug therapy*
  • Carcinoma, Hepatocellular / pathology
  • Carcinoma, Hepatocellular / surgery
  • Chemotherapy, Adjuvant
  • Hepatectomy*
  • Humans
  • Liver Neoplasms / drug therapy*
  • Liver Neoplasms / pathology
  • Liver Neoplasms / surgery
  • Male
  • Middle Aged
  • Neoadjuvant Therapy
  • Neoplasm Invasiveness
  • Niacinamide / analogs & derivatives
  • Phenylurea Compounds
  • Portal Vein / pathology*
  • Protein Kinase Inhibitors / administration & dosage*
  • Pyridines / administration & dosage*
  • Sorafenib
  • Time Factors
  • Tomography, X-Ray Computed
  • Treatment Outcome
  • Venous Thrombosis / drug therapy*
  • Venous Thrombosis / pathology
  • alpha-Fetoproteins / metabolism

Substances

  • AFP protein, human
  • Antineoplastic Agents
  • Benzenesulfonates
  • Phenylurea Compounds
  • Protein Kinase Inhibitors
  • Pyridines
  • alpha-Fetoproteins
  • Niacinamide
  • Sorafenib