Monoclonal gammopathy of undetermined significance (MGUS) and smoldering multiple myeloma (SMM): novel biological insights and development of early treatment strategies

被引:149
作者
Korde, Neha [1 ]
Kristinsson, Sigurdur Y. [3 ]
Landgren, Ola [2 ]
机构
[1] NHLBI, Hematol Branch, NIH, Bethesda, MD 20892 USA
[2] NCI, Med Oncol Branch, NIH, Ctr Canc Res, Bethesda, MD 20892 USA
[3] Karolinska Univ Hosp & Inst, Hematol Ctr, Stockholm, Sweden
基金
美国国家卫生研究院;
关键词
INDEPENDENT RISK-FACTOR; LIGHT-CHAIN RATIO; WORKING GROUP; EARLY-DIAGNOSIS; RAS MUTATIONS; LONG-TERM; FOLLOW-UP; PROGRESSION; DISEASE; PATHOGENESIS;
D O I
10.1182/blood-2011-01-270140
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Monoclonal gammopathy of unknown significance (MGUS) and smoldering multiple myeloma (SMM) are asymptomatic plasma cell dyscrasias, with a propensity to progress to symptomatic MM. In recent years there have been improvements in risk stratification models (involving molecular markers) of both disorders, which have led to better understanding of the biology and probability of progression of MGUS and SMM. In the context of numerous molecular events and heterogeneous risk of progression, developing individualized risk profiles for patients with MGUS and SMM represents an ongoing challenge that has to be addressed by prospective clinical monitoring and extensive correlative science. In this review we discuss the current standard of care of patients with MGUS and SMM, the use of risk models, including flow cytometry and free-light chain analyses, for predicting risk of progression. Emerging evidence from molecular studies on MGUS and SMM, involving cytogenetics, gene-expression profiling, and microRNA as well as molecular imaging is described. Finally, future directions for improving individualized management of MGUS and SMM patients, as well as the potential for developing early treatment strategies designed to delay and prevent development of MM are discussed. (Blood. 2011; 117(21): 5573-5581)
引用
收藏
页码:5573 / 5581
页数:9
相关论文
共 66 条
[51]   New criteria to identify risk of progression in monoclonal gammopathy of uncertain significance and smoldering multiple myeloma based on multiparameter flow cytometry analysis of bone marrow plasma cells [J].
Perez-Persona, Ernesto ;
Vidriales, Maria-Belen ;
Mateo, Gema ;
Garcia-Sanz, Ramon ;
Mateos, Maria-Victoria ;
de Coca, Alfonso Garcia ;
Galende, Josefina ;
Martin-Nunez, Guillermo ;
Alonso, Jose M. ;
de las Heras, Natalia ;
Hernandez, Jose M. ;
Martin, Alejandro ;
Lopez-Berges, Consuelo ;
Orfao, Alberto ;
San Miguel, Jesus F. .
BLOOD, 2007, 110 (07) :2586-2592
[52]   MicroRNAs regulate critical genes associated with multiple myeloma pathogenesis [J].
Pichiorri, Flavia ;
Suh, Sung-Suk ;
Ladetto, Marco ;
Kuehl, Michael ;
Palumbo, Tiziana ;
Drandi, Daniela ;
Taccioli, Cristian ;
Zanesi, Nicola ;
Alder, Hansjuerg ;
Hagan, John P. ;
Munker, Reinhold ;
Volinia, Stefano ;
Boccadoro, Mario ;
Garzon, Ramiro ;
Palumbo, Antonio ;
Aqeilan, Rami I. ;
Croce, Carlo M. .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2008, 105 (35) :12885-12890
[53]   Advances in the Diagnosis, Classification, Risk Stratification, and Management of Monoclonal Gammopathy of Undetermined Significance: Implications for Recategorizing Disease Entities in the Presence of Evolving Scientific Evidence [J].
Rajkumar, S. Vincent ;
Kyle, Robert A. ;
Buadi, Francis K. .
MAYO CLINIC PROCEEDINGS, 2010, 85 (10) :945-948
[54]   Serum free light chain ratio is an independent risk factor for progression in monoclonal gammopathy of undetermined significance [J].
Rajkumar, SV ;
Kyle, RA ;
Therneau, TM ;
Melton, LJ ;
Bradwell, AR ;
Clark, RJ ;
Larson, DR ;
Plevak, MF ;
Dispenzieri, A ;
Katzmann, JA .
BLOOD, 2005, 106 (03) :812-817
[55]   Thalidomide for previously untreated indolent or smoldering multiple myeloma [J].
Rajkumar, SV ;
Dispenzieri, A ;
Fonseca, R ;
Lacy, MQ ;
Geyer, S ;
Lust, JA ;
Kyle, RA ;
Greipp, PR ;
Gertz, MA ;
Witzig, TE .
LEUKEMIA, 2001, 15 (08) :1274-1276
[56]   Possible roles for activating RAS mutations in the MGUS to MM transition and in the intramedullary to extramedullary transition in some plasma cell tumors [J].
Rasmussen, T ;
Kuehl, M ;
Lodahl, M ;
Johnsen, HE ;
Dahl, IMS .
BLOOD, 2005, 105 (01) :317-323
[57]   Chromosomal abnormalities clustering in multiple myeloma reveals cytogenetic subgroups with nonrandom acquisition of chromosomal changes [J].
Sáez, B ;
Martín-Subero, JI ;
Guillén-Grima, F ;
Odero, MD ;
Prosper, F ;
Cigudosa, JC ;
Harder, L ;
Calasanz, MJ ;
Siebert, R .
LEUKEMIA, 2004, 18 (03) :654-657
[58]   Further cytogenetic characterization of multiple myeloma confirms that 14q32 translocations are a very rare event in hyperdiploid cases [J].
Smadja, NV ;
Leroux, D ;
Soulier, J ;
Dumont, S ;
Arnould, C ;
Taviaux, S ;
Taillemite, JL ;
Bastard, C .
GENES CHROMOSOMES & CANCER, 2003, 38 (03) :234-239
[59]   Chromosomal analysis in multiple myeloma: cytogenetic evidence of two different diseases [J].
Smadja, NV ;
Fruchart, C ;
Isnard, F ;
Louvet, C ;
Dutel, JL ;
Cheron, N ;
Grange, MJ ;
Monconduit, M ;
Bastard, C .
LEUKEMIA, 1998, 12 (06) :960-969
[60]   Increased risk of monoclonal gammopathy in first-degree relatives of patients with multiple myeloma or monoclonal gammopathy of undetermined significance [J].
Vachon, Celine M. ;
Kyle, Robert A. ;
Therneau, Terry M. ;
Foreman, Barbara J. ;
Larson, Dirk R. ;
Colby, Colin L. ;
Phelps, Tara K. ;
Dispenzieri, Angela ;
Kumar, Shaji K. ;
Katzmann, Jerry A. ;
Rajkumar, S. Vincent .
BLOOD, 2009, 114 (04) :785-790