IMiDs,A Novel Group of Small Molecule Drugs with Potent,Clinical Activity against a Variety of Hemat

来源 :BIT Life Sciences 1st Annual World Cancer Congess-2008(2008中 | 被引量 : 0次 | 上传用户:lu123127
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  On the basis of its immunomodulatory and antiangiogenic properties thalidomide has undergone clinical evaluation in various malignancies, including multiple myeloma, myelodysplastic syndromes, and other hematological and solid tumors.To date it has been awarded regulatory approval for use in multiple myeloma in both the USA and recently in Europe.Structural analogs of thalidomide have been synthesized in order to explore potential molecular targets of thalidomide, as well as to identify new therapeutic areas.One class of analogs (IMiDs) is several thousand times more potent than thalidomide in regulating cytokines, stimulating T-cell proliferation, inhibiting angiogenesis, etc.Lenalidomide (Revlimid(R)) is an immunomodulatory and anti-angiogenic, second generation IMiD analog of thalidomide.Preclinical testing, including pharmacology, PK and toxicity studies has led to the identification of Revlimid as a potent drug candidate for use in oncology.Revlimid is an oral agent with an enhanced activity profile compared to thalidomide and is a compound with multiple activities of potential relevance to cancer.
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