Management of Monoclonal Gammopathy of Undetermined Significance (MGUS) and Smoldering Multiple Myeloma (SMM)

被引:0
作者
Kyle, Robert A. [1 ]
Buadi, Francis [1 ]
Rajkumar, S. Vincent [1 ]
机构
[1] Mayo Clin, Div Hematol, Rochester, MN 55905 USA
来源
ONCOLOGY-NEW YORK | 2011年 / 25卷 / 07期
基金
美国国家卫生研究院;
关键词
CIRCULATING PLASMA-CELLS; INDEPENDENT RISK-FACTOR; LIGHT-CHAIN RATIO; MALIGNANT-TRANSFORMATION; FOLLOW-UP; NATURAL-HISTORY; FLOW-CYTOMETRY; LONG-TERM; PROGRESSION; POPULATION;
D O I
暂无
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Monoclonal gammopathy of undetermined significance (MGUS) is defined as a serum M protein level of less than 3 g/dL, less than 10% clonal plasma cells in the bone marrow, and the absence of end-organ damage. The prevalence of MGUS is 3.2% in the white population but is approximately twice that high in the black population. MGUS may progress to multiple myeloma, AL amyloidosis, Waldenstrom macroglobulinemia, or lymphoma. The risk of progression is approximately 1% per year, but the risk continues even after more than 25 years of observation. Risk factors for progression include the size of the serum M protein, the type of serum M protein, the number of plasma cells in the bone marrow, and the serum free light chain ratio. Smoldering (asymptomatic) multiple myeloma (SMM) is characterized by the presence of an M protein level of 3 g/dL or higher and/or 10% or more monoclonal plasma cells in the bone marrow but no evidence of end-organ damage. The overall risk of progression to a malignant condition is 10% per year for the first 5 years, approximately 3% per year for the next 5 years, and 1% to 2% per year for the following 10 years. Patients with both MGUS and SMM must be followed up for their lifetime.
引用
收藏
页码:578 / 586
页数:9
相关论文
共 50 条
[1]   Clinically relevant end points and new drug approvals for myeloma [J].
Anderson, K. C. ;
Kyle, R. A. ;
Rajkumar, S. V. ;
Stewart, A. K. ;
Weber, D. ;
Richardson, P. .
LEUKEMIA, 2008, 22 (02) :231-239
[2]  
AXELSSON U, 1986, ACTA MED SCAND, V219, P519
[3]  
AXELSSON U, 1966, ACTA MED SCAND, V179, P235
[4]   Role of different hematologic variables in defining the risk of malignant transformation in monoclonal gammopathy [J].
Baldini, L ;
Guffanti, A ;
Cesana, BM ;
Colombi, M ;
Chiorboli, O ;
Damilano, I ;
Maiolo, AT .
BLOOD, 1996, 87 (03) :912-918
[5]   Monoclonal gammopathy of undetermined significance: a consensus statement [J].
Berenson, James R. ;
Anderson, Kenneth C. ;
Audell, Robert A. ;
Boccia, Ralph V. ;
Coleman, Morton ;
Dimopoulos, Meletios A. ;
Drake, Matthew T. ;
Fonseca, Rafael ;
Harousseau, Jean-Luc ;
Joshua, Douglas ;
Lonial, Sagar ;
Niesvizky, Ruben ;
Palumbo, Antonio ;
Roodman, G. David ;
San-Miguel, Jesus F. ;
Singhal, Seema ;
Weber, Donna M. ;
Zangari, Maurizio ;
Wirtschafter, Eric ;
Yellin, Ori ;
Kyle, Robert A. .
BRITISH JOURNAL OF HAEMATOLOGY, 2010, 150 (01) :28-38
[6]   Impact of optimal follow-up of monoclonal gammopathy of undetermined significance on early diagnosis and prevention of myeloma-related complications [J].
Bianchi, Giada ;
Kyle, Robert A. ;
Colby, Colin L. ;
Larson, Dirk R. ;
Kumar, Shaji ;
Katzmann, Jerry A. ;
Dispenzieri, Angela ;
Therneau, Terry M. ;
Cerhan, James R. ;
Melton, L. Joseph, III ;
Rajkumar, S. Vincent .
BLOOD, 2010, 116 (12) :2019-2025
[7]   MALIGNANT TRANSFORMATION AND LIFE EXPECTANCY IN MONOCLONAL GAMMOPATHY OF UNDETERMINED SIGNIFICANCE [J].
BLADE, J ;
LOPEZGUILLERMO, A ;
ROZMAN, C ;
CERVANTES, F ;
SALGADO, C ;
AGUILAR, JL ;
VIVESCORRONS, JL ;
MONTSERRAT, E .
BRITISH JOURNAL OF HAEMATOLOGY, 1992, 81 (03) :391-394
[8]   Prognostic factors for malignant transformation in monoclonal gammopathy of undetermined significance and smoldering multiple myeloma [J].
Cesana, C ;
Klersy, C ;
Barbarano, L ;
Nosari, AM ;
Crugnola, M ;
Pungolino, E ;
Gargantini, L ;
Granata, S ;
Valentini, M ;
Morra, E .
JOURNAL OF CLINICAL ONCOLOGY, 2002, 20 (06) :1625-1634
[9]   The relationship between monoclonal gammopathy of undetermined significance and venous thromboembolic disease [J].
Cohen, Adam L. ;
Sarid, Rami .
THROMBOSIS RESEARCH, 2010, 125 (03) :216-219
[10]  
Cohen HJ, 1998, AM J MED, V105, P362