International Myeloma Working Group consensus approach to the treatment of multiple myeloma patients who are candidates for autologous stem cell transplantation

M Cavo, SV Rajkumar, AA Palumbo, P Moreau, R Orlowski, J Blade, O Sezer, H Ludwig, MA Dimopoulos, M Attal, Pieter Sonneveld, M Boccadoro, KC Anderson, PG Richardson, W Bensinger, HE Johnsen, N Kroeger, G Gahrton, PL Bergsagel, DH VesoleH Einsele, S Jagannath, R Niesvizky, BGM Durie, J San Miguel, S Lonial

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The role of high-dose therapy followed by autologous stem cell transplantation (ASCT) in the treatment of multiple myeloma (MM) continues to evolve in the novel agent era. The choice of induction therapy has moved from conventional chemotherapy to newer regimens incorporating the immunomodulatory derivatives thalidomide or lenalidomide and the proteasome inhibitor bortezomib. These drugs combine well with traditional therapies and with one another to form various doublet, triplet, and quadruplet regimens. Up-front use of these induction treatments, in particular 3-drug combinations, has affected unprecedented rates of complete response that rival those previously seen with conventional chemotherapy and subsequent ASCT. Autotransplantation applied after novel-agent-based induction regimens provides further improvement in the depth of response, a gain that translates into extended progression-free survival and, potentially, overall survival. High activity shown by immunomodulatory derivatives and bortezomib before ASCT has recently led to their use as consolidation and maintenance therapies after autotransplantation. Novel agents and ASCT are complementary treatment strategies for MM. This article reviews the current literature and provides important perspectives and guidance on the major issues surrounding the optimal current management of younger, transplantation-eligible MM patients. (Blood. 2011;117(23):6063-6073)
Original languageUndefined/Unknown
Pages (from-to)6063-6073
Number of pages11
Issue number23
Publication statusPublished - 2011

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  • EMC MM-02-41-03

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