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This activity is part of PER's Integrated Oncology Learning Series: A Focus on Multiple Myeloma

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Continuing Education Information

Physicians’ Education Resource is accredited by the Accreditation Council for Continuing Medical Education to provide continuing medical education for physicians.

Physicians’ Education Resource designates this educational activity for a maximum of 1.25 AMA PRA Category 1 Credit(s)™. Physicians should only claim credit commensurate with the extent of their participation in the activity.

New Regimens, Emerging Approaches, and Novel Agents for the Treatment of Multiple Myeloma

Cancer Summaries & Commentaries

1.25 AMA PRA Category 1 Credit(s)
Release Date: March 19, 2010
Expiration Date: March 19, 2011

Upon completion of this educational activity, you should be able to:

  • Assess the efficacy and safety of induction therapy with regimens comprising an immunomodulatory agent and/or proteasome inhibitor followed by maintenance therapy in elderly patients with newly diagnosed MM
  • Assess the efficacy of a proteasome inhibitor plus a glucocorticoid as induction therapy in newly diagnosed MM
  • Compare the efficacy and safety of consolidation using a therapeutic regimen containing an immunomodulatory agent with high-dose chemotherapy/autologous stem cell transplantation after induction therapy in newly diagnosed MM
  • Compare the efficacy of induction with conventional chemotherapy with or without an immunomodulatory agent followed by maintenance therapy in elderly patients with newly diagnosed MM
  • Evaluate the efficacy and safety of a second-generation proteasome inhibitor in relapsed/refractory MM
  • Assess the safety and efficacy of a novel immunomodulatory agent in relapsed/refractory MM
  • Evaluate the efficacy and safety of combining an HSP90 inhibitor with a proteasome inhibitor in relapsed/refractory MM
  • Assess the feasibility of combining an anti-CS1 MoAb with an immunomodulatory agent or proteasome inhibitor in relapsed/refractory MM

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Educational Grants

An educational grant for this activity was provided by:


  1. Bristol-Myers Squibb
  2. Celgene Corporation