LEADER 02312nam 2200517 a 450 001 9910790451003321 005 20230801221556.0 010 $a1-60805-297-4 035 $a(CKB)2670000000148694 035 $a(EBL)864207 035 $a(OCoLC)779141401 035 $a(SSID)ssj0000942934 035 $a(PQKBManifestationID)11492225 035 $a(PQKBTitleCode)TC0000942934 035 $a(PQKBWorkID)10976890 035 $a(PQKB)11670260 035 $a(OCoLC)785783102 035 $a(MiAaPQ)EBC864207 035 $a(EXLCZ)992670000000148694 100 $a20120315d2012 uy 0 101 0 $aeng 135 $aur|n|---||||| 181 $ctxt 182 $cc 183 $acr 200 00$aMultiple myeloma$b[electronic resource] $ea new era of treatment strategies /$feditors, Klaus Podar, Kenneth C. Anderson 210 $a[U.S.A.] $cBentham Science Publishers$d[2012] 215 $a1 online resource (217 p.) 300 $aDescription based upon print version of record. 311 $a1-60805-609-0 320 $aIncludes bibliographical references and index. 327 $asection 1. Multiple myeloma -- section 2. Treatment guidelines -- section 3. The bone marrow microenvironment and the pathogenesis of multiple myeloma -- section 4. New treatment strategies. 330 $aMultiple Myeloma (MM), the second most common blood cancer in adults, is a clonal plasma cell malignancy within the bone marrow characterized by osteolytic bone lesions, renal disease, and immunodeficiency. It is now well established that MM cell- induced disruption of the bone marrow homeostasis between the highly organized cellular and extracellular compartments supports MM cell proliferation, survival, migration, and drug resistance via activation of various signaling pathways. Based on this knowledge, the prototypic drugs thalidomide, bortezomib, and lenalidomide, which target both MM cell 606 $aMultiple myeloma$xTreatment 615 0$aMultiple myeloma$xTreatment. 676 $a616.99/418 676 $a616.99418 701 $aPodar$b Klaus$01522445 701 $aAnderson$b Kenneth C$0876632 801 0$bMiAaPQ 801 1$bMiAaPQ 801 2$bMiAaPQ 906 $aBOOK 912 $a9910790451003321 996 $aMultiple myeloma$93762155 997 $aUNINA