Tivantinib: a new promising mesenchymal-epithelial transition factor inhibitor in the treatment of hepatocellular carcinoma

Future Oncol. 2013 Feb;9(2):153-65. doi: 10.2217/fon.12.188.

Abstract

Tivantinib (ARQ 197) is an orally administered, selective small molecule that inhibits mesenchymal-epithelial transition factor (MET) via a novel, ATP-independent binding mechanism. Preclinical studies demonstrated that tivantinib has a broad-spectrum anti-tumor activity, especially in cells expressing high levels of MET. A randomized Phase II study in second-line hepatocellular carcinoma showed statistically significant improvement in time to progression with tivantinib compared to a placebo. Noteworthy, a significant pronounced benefit in time to progression and overall survival was observed in MET-high patients. In addition, MET expression was defined as a negative prognostic factor. The most frequent adverse events were hematologic events. A Phase III study in the MET-high hepatocellular carcinoma is actively recruiting patients. Phase II and III studies in non-small-cell lung cancer and colorectal cancer are ongoing.

MeSH terms

  • Animals
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / chemistry
  • Antineoplastic Agents / pharmacology
  • Antineoplastic Agents / therapeutic use*
  • Carcinoma, Hepatocellular / drug therapy*
  • Clinical Trials, Phase I as Topic
  • Clinical Trials, Phase II as Topic
  • Drug Evaluation, Preclinical
  • Humans
  • Liver Neoplasms / drug therapy*
  • Pyrrolidinones / adverse effects
  • Pyrrolidinones / chemistry
  • Pyrrolidinones / pharmacology
  • Pyrrolidinones / therapeutic use*
  • Quinolines / adverse effects
  • Quinolines / chemistry
  • Quinolines / pharmacology
  • Quinolines / therapeutic use*
  • Treatment Outcome

Substances

  • ARQ 197
  • Antineoplastic Agents
  • Pyrrolidinones
  • Quinolines