Pilot study: rapamycin in advanced hepatocellular carcinoma

Aliment Pharmacol Ther. 2010 Sep;32(6):763-8. doi: 10.1111/j.1365-2036.2010.04404.x.

Abstract

Background: The PI3K/Akt/mTOR signal pathway is involved in hepatocarcinogenesis. Rapamycin (=sirolimus), a specific mTOR inhibitor, leads to G(1) arrest of many malignant cell lines and currently, analogues of rapamycin are being investigated as a cancer chemotherapeutic adjuvant.

Aim: To study the toxicity and tolerability of rapamycin therapy in patients with advanced hepatocellular carcinoma (HCC).

Methods: Between June 2005 and February 2007, patients with advanced HCC, not eligible for any established therapy, were included in the study.

Results: Eighteen patients (F/M: 5/13) with compensated liver cirrhosis (Child A n = 11, Child B n = 5, Child C n = 2) and histologically proven HCC were included in this study. According to the BCLC staging system, most of the patients enrolled had an advanced HCC: BCLC stage B: n = 2, Barcelona Clinic Liver-Cancer (BCLC) stage C: n = 14, BCLC stage D: n = 2. Overall, therapy with rapamycin was well tolerated. Most common toxicities were thrombocytopaenia and anaemia. We did not observe any partial or complete tumour response. At 3 months, two patients had stable disease and at 6 months, all patients had progressed. The median overall survival was 5.27 months, median time to progression was 3 months.

Conclusion: Rapamycin is well tolerated in patients with advanced HCC, but only minimally effective.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Carcinoma, Hepatocellular / drug therapy*
  • Disease Progression
  • Female
  • Humans
  • Immunosuppressive Agents / therapeutic use*
  • Liver Cirrhosis / drug therapy*
  • Liver Neoplasms / drug therapy*
  • Male
  • Middle Aged
  • Pilot Projects
  • Sirolimus / therapeutic use*
  • Treatment Outcome

Substances

  • Immunosuppressive Agents
  • Sirolimus