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
相关论文
共 137 条
[61]  
Jourdan M, 1999, EUR CYTOKINE NETW, V10, P65
[62]   Analysis of circulating tumor cells in patients with multiple myeloma during the course of high-dose therapy with peripheral blood stem cell transplantation [J].
Kiel, K ;
Cremer, FW ;
Rottenburger, C ;
Kallmeyer, C ;
Ehrbrecht, E ;
Atzberger, A ;
Hegenbart, U ;
Goldschmidt, H ;
Moos, M .
BONE MARROW TRANSPLANTATION, 1999, 23 (10) :1019-1027
[63]   STUDIES ON THE CLONAL ORIGIN OF MULTIPLE-MYELOMA - USE OF INDIVIDUALLY SPECIFIC (IDIOTYPE) ANTIBODIES TO TRACE THE ONCOGENIC EVENT TO ITS EARLIEST POINT OF EXPRESSION IN B-CELL DIFFERENTIATION [J].
KUBAGAWA, H ;
VOGLER, LB ;
CAPRA, JD ;
CONRAD, ME ;
LAWTON, AR ;
COOPER, MD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1979, 150 (04) :792-807
[64]   Improved survival in multiple myeloma and the impact of novel therapies [J].
Kumar, Shaji K. ;
Rajkumar, S. Vincent ;
Dispenzieri, Angela ;
Lacy, Martha Q. ;
Hayman, Suzanne R. ;
Buadi, Francis K. ;
Zeldenrust, Steven R. ;
Dingli, David ;
Russell, Stephen J. ;
Lust, John A. ;
Greipp, Philip R. ;
Kyle, Robert A. ;
Gertz, Morie A. .
BLOOD, 2008, 111 (05) :2516-2520
[65]   Clinical course of patients with relapsed multiple myeloma [J].
Kumar, SK ;
Therneau, TM ;
Gertz, MA ;
Lacy, MQ ;
Dispenzieri, A ;
Rajkumar, SV ;
Fonseca, R ;
Witzig, TE ;
Lust, JA ;
Larson, DR ;
Kyle, RA ;
Greipp, PR .
MAYO CLINIC PROCEEDINGS, 2004, 79 (07) :867-874
[66]   Drug therapy: Multiple myeloma [J].
Kyle, RA ;
Rajkumar, SV .
NEW ENGLAND JOURNAL OF MEDICINE, 2004, 351 (18) :1860-1873
[67]   Review of 1027 patients with newly diagnosed multiple myeloma [J].
Kyle, RA ;
Gertz, MA ;
Witzig, TE ;
Lust, JA ;
Lacy, MQ ;
Dispenzieri, A ;
Fonseca, R ;
Rajkumar, SV ;
Offord, JR ;
Larson, DR ;
Plevak, ME ;
Therneau, TM ;
Greipp, PR .
MAYO CLINIC PROCEEDINGS, 2003, 78 (01) :21-33
[68]   A long-term study of prognosis in monoclonal gammopathy of undetermined significance [J].
Kyle, RA ;
Therneau, TM ;
Rajkumar, SV ;
Offord, JR ;
Larson, DR ;
Plevak, MF ;
Melton, L .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (08) :564-569
[69]   The significance of monoclonal gammopathy of undetermined significance [J].
Kyle, Robert A. ;
Kumar, Shaji .
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL, 2009, 94 (12) :1641-1644
[70]   Pomalidomide (CC4047) plus low dose dexamethasone (Pom/dex) is active and well tolerated in lenalidomide refractory multiple myeloma (MM) [J].
Lacy, M. Q. ;
Hayman, S. R. ;
Gertz, M. A. ;
Short, K. D. ;
Dispenzieri, A. ;
Kumar, S. ;
Greipp, P. R. ;
Lust, J. A. ;
Russell, S. J. ;
Dingli, D. ;
Zeldenrust, S. ;
Fonseca, R. ;
Bergsagel, P. L. ;
Roy, V. ;
Mikhael, J. R. ;
Stewart, A. K. ;
Laumann, K. ;
Allred, J. B. ;
Mandrekar, S. J. ;
Rajkumar, S. V. ;
Buadi, F. .
LEUKEMIA, 2010, 24 (11) :1934-1939