Abstract

The introduction of autologous stem cell transplantation combined with the introduction of immunomodulatory drugs (IMiDs) and proteasome inhibitors has significantly improved survival of multiple myeloma patients. However, ultimately the majority of patients will develop refractory disease, indicating the need for new treatment modalities. In preclinical and clinical studies, promising results have been obtained with several monoclonal antibodies (mAbs) targeting the myeloma tumor cell or the bone marrow microenvironment. The mechanisms underlying the therapeutic efficacy of these mAbs include direct induction of tumor cell apoptosis via inhibition or activation of target molecules, complement-dependent cytotoxicity and antibody-dependent cell-mediated cytotoxicity (ADCC). The capability of IMiDs to enhance ADCC and the modulation of various important signaling cascades in myeloma cells by both bortezomib and IMiDs forms the rationale to combine these novel agents with mAbs as new treatment strategies for myeloma patients. In this review, we will give an overview of various mAbs directly targeting myeloma tumor cells or indirectly via effects on the bone marrow microenvironment. Special focus will be on the combination of these mAbs with IMiDs or bortezomib.

Highlights

  • The introduction of autologous stem cell transplantation and novel agents such as the proteasome inhibitor bortezomib and the immunomodulatory drugs (IMiDs) thalidomide and lenalidomide has significantly improved survival of myeloma patients.[1]

  • The successful application of immunotherapeutics such as the anti-CD20 monoclonal antibody rituximab, the anti-CD52 mAb alemtuzumab and, most recently, the anti-CD30–drug conjugate brentuximab vedotin in non-Hodgkin’s lymphoma, Hodgkin’s lymphoma and chronic lymphocytic leukemia has stimulated the development of mAbs applicable for myeloma treatment

  • The process of antibodydependent cell-mediated cytotoxicity (ADCC) is achieved through activation of Fc receptors on myeloid and natural killer (NK) effector cells by tumor cellattached immunoglobins

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Summary

Introduction

The introduction of autologous stem cell transplantation and novel agents such as the proteasome inhibitor bortezomib and the immunomodulatory drugs (IMiDs) thalidomide and lenalidomide has significantly improved survival of myeloma patients.[1].

Results
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