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KAMAKSHI V. RAO, PHARM.D., BCOP, is Hematology/Oncology Clinical Specialist, Department of Pharmacy, University of North Carolina Hospitals and Clinics, 101 Manning Drive, CB 7600, Chapel Hill, NC 27514 (kvrao{at}unch.unc.edu).

Purpose. The pharmacology, clinical use, adverse effects, dosage and administration, and cost of lenalidomide in the treatment of multiple myeloma (MM) are reviewed. Summary. Lenalidomide is an analogue of thalidomide and has been shown to be more potent than thalidomide in the stimulation of T-cell, interleukin-2, and interferon- production. Both drugs have direct cytotoxic effects on myeloma cells and are capable of inducing apoptosis. They are also capable of reducing angiogenesis through the inhibition of the secretion of vascular endothelial growth factor (VEGF). Inhibition of VEGF leads to alterations in the microvasculature of the bone marrow environment and inhibits myeloma cell growth and proliferation. Unlike thalidomide, lenalidomide has almost no sedative or constipative properties and induces only minimal neurotoxicity; however, there is concern about lenalidomide’s teratogenic potential. Phase I, II, and III trials have been carried out with lenalidomide in patients with relapsed or refractory MM, and the drug has shown impressive response rates in relapsed disease. The combination of lenalidomide and dexamethasone has shown superior patient survival. Lenalidomide’s efficacy in newly diagnosed MM is currently being studied. Neutropenia and thrombocytopenia were found to be the most common grade 3 or higher toxicities. Rates of these toxicities varied among trials and may have been affected by the setting in which lenalidomide was used (i.e., relapsed or refractory disease versus newly diagnosed MM). Conclusion. Lenalidomide, a thalidomide analogue, has produced good results when used with dexamethasone in patients with relapsed or refractory MM. Lenalidomide is associated with hematologic toxicities, and participation in a restricted-distribution program is required of prescribers, pharmacies, and patients because of the drug’s teratogenic potential. Index terms: Antineoplastic agents; Combined therapy; Costs; Dexamethasone; Dosage; Drug administration; Lenalidomide; Mechanism of action; Multiple myeloma; Pregnancy; Steroids, cortico-; Teratogenicity

 

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				I. G. Glezerman, T. Kewalramani, and K. Jhaveri Reversible Fanconi syndrome due to lenalidomide NDT Plus, August 1, 2008; 1(4): 215 - 217. [Full Text] [PDF]