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Clinical development of panobinostat in classical Hodgkin's lymphoma.

Abstract
Deacetylase (DAC) inhibitors are promising new anticancer drugs that have complex mechanisms of action, including induction of cell-cycle arrest and apoptosis, inhibition of angiogenesis and induction of a favorable anti-tumor immune response. Panobinostat, a potent inhibitor of DAC 1-11 enzymatic activity, has demonstrated a significant in vitro antiproliferative activity against classical Hodgkin's lymphoma (cHL) cell lines in addition to a promising clinical activity in early Phase I studies in patients with relapsed cHL. In a recently completed large Phase II study in patients with relapsed cHL, panobinostat reduced tumor measurements in 74% of patients, including 23% partial and 4% complete remissions. In this article, we review the status of panobinostat drug development and compare its activity to those of other DAC inhibitors in patients with relapsed cHL. Future investigations should focus on designing rational combination regimens and identifying predictive markers that will assist in selecting patients who are likely to benefit from this novel therapy.
AuthorsYasuhiro Oki, Amanda Copeland, Anas Younes
JournalExpert review of hematology (Expert Rev Hematol) Vol. 4 Issue 3 Pg. 245-52 (Jun 2011) ISSN: 1747-4094 [Electronic] England
PMID21668391 (Publication Type: Journal Article, Review)
Chemical References
  • Benzamides
  • Histone Deacetylase Inhibitors
  • Hydroxamic Acids
  • Indoles
  • Pyridines
  • Pyrimidines
  • entinostat
  • Vorinostat
  • Panobinostat
  • mocetinostat
  • Histone Deacetylases
Topics
  • Benzamides (chemistry, pharmacokinetics, therapeutic use)
  • Clinical Trials as Topic
  • Drug Evaluation, Preclinical
  • Histone Deacetylase Inhibitors (chemistry, pharmacokinetics, therapeutic use)
  • Histone Deacetylases (chemistry, metabolism)
  • Hodgkin Disease (drug therapy)
  • Humans
  • Hydroxamic Acids (chemistry, pharmacokinetics, therapeutic use)
  • Indoles
  • Panobinostat
  • Pyridines (chemistry, pharmacokinetics, therapeutic use)
  • Pyrimidines (chemistry, pharmacokinetics, therapeutic use)
  • Vorinostat

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