AI Article Synopsis

  • Recent advancements in treating Waldenström's macroglobulinemia (WM) focus on novel therapeutic agents.
  • Key therapeutic targets include the PI3K/Akt/mTOR pathway, PKC pathways, NF-kB signaling, tyrosine kinases, and histone deacetylase inhibitors.
  • The review highlights the clinical development of these agents and their potential to improve WM treatment.

Article Abstract

Within the past few years, major advances in the preclinical and clinical testing of novel therapeutic agents have occurred in Waldenström's macroglobulinemia (WM). These include agents that target the PI3K/Akt/mTOR pathway, PKC pathways, NF-kB signaling pathway, as well as tyrosine kinases and histone deacetylase inhibitors. In this review, we summarize the current understanding of the clinical development of these agents in WM.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3133646PMC
http://dx.doi.org/10.3816/CLM.2009.n.022DOI Listing

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