An open-label, Phase I study of cediranib (RECENTIN) in patients with acute myeloid leukemia

Leuk Res. 2010 Feb;34(2):196-202. doi: 10.1016/j.leukres.2009.07.020. Epub 2009 Aug 11.

Abstract

VEGFR and c-Kit signaling pathways may contribute to the pathophysiology of acute myeloid leukemia (AML). Thirty-five patients with AML received cediranib (RECENTIN), an oral, highly potent VEGF signaling inhibitor with c-Kit activity, at doses of < or =30 mg/day. The most common adverse events were diarrhea, hypertension and fatigue. Six patients experienced an objective response (3 each at 20 and 30 mg). Dose- and time-dependent reductions in sVEGFR-2 were observed, and there was a positive correlation between cediranib exposure and the change in plasma VEGF levels from baseline. Cediranib was generally well tolerated and showed preliminary evidence of activity as a monotherapy.

Publication types

  • Clinical Trial, Phase I
  • Multicenter Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • Diarrhea / chemically induced
  • Fatigue / chemically induced
  • Female
  • Humans
  • Hypertension / chemically induced
  • Leukemia, Myeloid, Acute / complications
  • Leukemia, Myeloid, Acute / drug therapy*
  • Male
  • Middle Aged
  • Pilot Projects
  • Proto-Oncogene Proteins c-kit / drug effects
  • Quinazolines / administration & dosage*
  • Quinazolines / adverse effects
  • Quinazolines / therapeutic use
  • Signal Transduction / drug effects
  • Treatment Outcome
  • Vascular Endothelial Growth Factor Receptor-2 / drug effects

Substances

  • Quinazolines
  • Proto-Oncogene Proteins c-kit
  • Vascular Endothelial Growth Factor Receptor-2
  • cediranib