| Literature DB >> 29748955 |
Cindy Varga1, Jacob P Laubach2, Kenneth C Anderson2, Paul G Richardson2.
Abstract
The treatment of multiple myeloma (MM) has gone through several major advances over the last 5 years with the introduction of next generation proteasome inhibitors (PI; carfilzomib, ixazomib) and immunomodulatory derivatives (IMiD; pomalidomide), with these new agents having a substantial impact on patient outcome. However, despite these advances, MM remains a highly resistant disease given its propensity for clonal heterogeneity and its complex interaction with the surrounding bone marrow microenvironment. Almost all patients eventually relapse despite therapeutic responses to a PI, IMiD or both. With the regulatory approval of the monoclonal antibodies Daratumumab and Elotuzumab in 2015, impressive and durable responses are being observed, even in heavily pre-treated patients who have exhausted other therapeutic options, suggesting immunological approaches in this setting have real merit. This review will focus on newer monoclonal antibodies and chimeric-antigen receptor (CAR) T cell strategies currently under investigation and in various stages of clinical development.Entities:
Keywords: zzm321990BCMAzzm321990; Isatuximab; Siltuximab; monoclonal antibodies; multiple myeloma
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Year: 2018 PMID: 29748955 DOI: 10.1111/bjh.15116
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998