Pharmacodynamic considerations of small molecule targeted therapy for treating B-cell malignancies in the elderly

Expert Opin Drug Metab Toxicol. 2015;11(9):1371-91. doi: 10.1517/17425255.2015.1055246. Epub 2015 Jul 11.

Abstract

Introduction: Small molecule inhibitors are currently in various stages of preclinical and clinical trials and are expected to revolutionize the treatment of many neoplastic diseases, including B-cell lymphoid malignancies.

Areas covered: This article reviews the chemical structure, mechanisms of action, pharmacodynamic and pharmacokinetic properties, as well as clinical applications of small molecules in the treatment of elderly patients with B-cell hematological malignancies. Bibliographic research covering mainly the period from 2010 until February 2015 was conducted on the MEDLINE database for articles in English. Proceedings of the American Society of Hematology, European Hematology Association and American Society of Clinical Oncology conferences held during the last 5 years were also included.

Expert opinion: In the last few years, several preclinical and clinical trials have evaluated many small weight organic molecules which downregulate B-cell receptor (BCR) signaling and act via inhibition of either BCR-associated kinases or cyclin-dependent kinases, or which are antagonists of members of the B-cell lymphoma 2 protein family. Pharmacokinetic profiles of these agents as well as dosage used and adverse events in patients with lymphoid malignancies have been established. Some of these inhibitors satisfy therapeutic modalities as suitable for the elderly patients, including those with chronic lymphocytic leukemia and non-Hodgkin's lymphoma.

Keywords: B-cell malignancies; clinical efficacy; dinaciclib; fostamatinib; ibrutinib; idelalisib; navitoclax; pharmacokinetics; small molecules; venetoclax.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Aged
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / pharmacokinetics
  • Antineoplastic Agents / pharmacology*
  • Down-Regulation / drug effects
  • Drug Design
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Lymphoproliferative Disorders / drug therapy*
  • Lymphoproliferative Disorders / pathology
  • Molecular Targeted Therapy*
  • Receptors, Antigen, B-Cell / genetics
  • Signal Transduction / drug effects

Substances

  • Antineoplastic Agents
  • Receptors, Antigen, B-Cell