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Review Article| Volume 21, ISSUE 6, P1141-1156, December 2007

Management of Newly Diagnosed Myeloma

  • S. Vincent Rajkumar
    Correspondence
    Corresponding author. Division of Hematology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905.
    Affiliations
    Division of Hematology, Department of Internal Medicine, Mayo Clinic and Foundation, 200 First Street SW, Rochester, MN 55905, USA

    College of Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA
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  • Antonio Palumbo
    Affiliations
    Division of Hematology, University of Turin, Azienda Ospedaliera S. Giovanni Battista, Ospedale Molinette, Turin, Italy
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      The treatment of multiple myeloma has changed dramatically in the last decade with the introduction of thalidomide, bortezomib, and lenalidomide. Patients eligible for autologous stem cell transplantation (ASCT) are treated with non-alkylating agent–containing regimens as initial therapy; typically thalidomide-dexamethasone or lenalidomide-dexamethasone. For patients not eligible for ASCT, the current standard of care is melphalan, prednisone, and thalidomide. Ongoing trials will soon assess if combinations including melphalan and prednisone plus bortezomib or MP plus lenalidomide may be considered an attractive option. Patients who have risk factors, such as deletion 13 or translocation t(4;14) or t(14;16), are candidates for novel, more aggressive treatments.
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