Can we change the disease biology of multiple myeloma?

被引:45
作者
Borrello, Ivan [1 ]
机构
[1] Johns Hopkins Univ, Sch Med, Baltimore, MD 21231 USA
关键词
Multiple myeloma; Cell biology; Bone marrow microenvironment; Mode of action; Immunomodulatory drugs; Proteosome inhibitors; TUMOR-NECROSIS-FACTOR; NATURAL-KILLER-CELL; MARROW STROMAL CELLS; LENALIDOMIDE-INDUCED IMMUNOMODULATION; ENDOTHELIAL GROWTH-FACTOR; HIGH-DOSE THERAPY; BONE-MARROW; T-CELLS; CYTOKINE PRODUCTION; MONOCLONAL GAMMOPATHY;
D O I
10.1016/S0145-2126(12)70003-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Despite improvements in disease management, multiple myeloma (MM) remains incurable. Conventional treatment methods are unsatisfactory, leading to a pattern of regression and remission, and ultimately failure. This pattern suggests that one of the possible strategies for improving outcomes is continuous therapy to maintain suppression of the surviving tumor cells. Optimal management of MM requires potent agents and modalities with direct tumoricidal activity, which can also provide continuous suppression of the residual tumor to prevent disease relapse. Immunomodulatory agents exert immunomodulatory and tumoricidal effects, and cause disruption of stromal cell support from the bone marrow microenvironment. Therefore continuous therapy with immumomodulatory agents may be able to provide both tumor reduction and tumor suppression, enabling physicians to consider the possibility of incorporating continuous therapy into the treatment paradigm of patients with MM. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:S3 / S12
页数:10
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