Monoclonal Gammopathy of Undetermined Significance and Smoldering Multiple Myeloma: A Review of the Current Understanding of Epidemiology, Biology, Risk Stratification, and Management of Myeloma Precursor Disease

被引:72
作者
Agarwal, Amit [1 ]
Ghobrial, Irene M. [2 ]
机构
[1] Univ Arizona, Div Hematol Oncol, Tucson, AZ USA
[2] Harvard Univ, Sch Med, Dana Farber Canc Inst, Boston, MA 02215 USA
关键词
BONE-MARROW ENVIRONMENT; LIGHT-CHAIN RATIO; SIGNIFICANCE MGUS; PLASMA-CELLS; MALIGNANT-TRANSFORMATION; ADULT-POPULATION; NATURAL-HISTORY; PROGRESSION; PREVALENCE; PATHOGENESIS;
D O I
10.1158/1078-0432.CCR-12-2922
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
The term monoclonal gammopathy of undetermined significance (MGUS) was coined in 1978. The recent advances in our knowledge about MGUS and smoldering multiple myeloma (SMM) have helped us better understand the pathogenesis of myeloma. It seems that myeloma evolves from a precursor state in almost all cases. We do not completely understand the multistep process from the precursor state to myeloma, but studies like whole genome sequencing continue to improve our understanding of this process. The process of transformation may not be linear acquisition of changes, but rather a branched heterogeneous process. Clinical features that are prognostic of rapid transformation have been identified, but no specific molecular markers have been identified. Even with recent advances, multiple myeloma remains an incurable disease in the vast majority, and intervening at the precursor state provides a unique opportunity to alter the natural history of the disease. A limitation is that a vast majority of patients with precursor disease, especially low-risk MGUS, will never progress to myeloma in their lifetime, and treating these patients is not only unnecessary but may be potentially harmful. The challenge is to identify a subset of patients with the precursor state that would definitely progress to myeloma and in whom interventions will have a meaningful impact. As our understanding of the molecular and genetic processes improves, these studies will guide the selection of high-risk patients more appropriately and ultimately direct a tailored management strategy to either delay progression to symptomatic myeloma or even "cure" a person at this premalignant stage. Clin Cancer Res; 19(5); 985-94. (C) 2012 AACR.
引用
收藏
页码:985 / 994
页数:10
相关论文
共 72 条
[1]
Pathogenesis of Myeloma [J].
Anderson, Kenneth C. ;
Carrasco, Ruben D. .
ANNUAL REVIEW OF PATHOLOGY: MECHANISMS OF DISEASE, VOL 6, 2011, 6 :249-274
[2]
Avet-Loiseau H, 1999, CANCER RES, V59, P4546
[3]
Oncogenesis of multiple myeloma: 14q32 and 13q chromosomal abnormalities are not randomly distributed, but correlate with natural history, immunological features, and clinical presentation [J].
Avet-Loiseau, H ;
Facon, T ;
Grosbois, B ;
Magrangeas, F ;
Rapp, MJ ;
Harousseau, JL ;
Minvielle, S ;
Bataille, R .
BLOOD, 2002, 99 (06) :2185-2191
[4]
Rearrangements of the c-myc oncogene are present in 15% of primary human multiple myeloma tumors [J].
Avet-Loiseau, H ;
Gerson, F ;
Magrangeas, F ;
Minvielle, S ;
Harousseau, JL ;
Bataille, R .
BLOOD, 2001, 98 (10) :3082-3086
[5]
AXELSSON U, 1966, ACTA MED SCAND, V179, P235
[6]
Darwinian evolution and tiding clones in multiple myeloma [J].
Bahlis, Nizar J. .
BLOOD, 2012, 120 (05) :927-928
[7]
Seven-year median time to progression with thalidomide for smoldering myeloma: partial response identifies subset requiring earlier salvage therapy for symptomatic disease [J].
Barlogie, Bart ;
van Rhee, Frits ;
Shaughnessy, John D., Jr. ;
Epstein, Joshua ;
Yaccoby, Shmuel ;
Pineda-Roman, Mauricio ;
Hollmig, Klaus ;
Alsayed, Yazan ;
Hoering, Antje ;
Szymonifka, Jackie ;
Anaissie, Elias ;
Petty, Nathan ;
Kumar, Naveen S. ;
Srivastava, Geetika ;
Jenkins, Bonnie ;
Crowley, John ;
Zeldis, Jerome B. .
BLOOD, 2008, 112 (08) :3122-3125
[8]
Cyclin D dysregulation: an early and unifying pathogenic event in multiple myeloma [J].
Bergsagel, PL ;
Kuehl, WM ;
Zhan, FH ;
Sawyer, J ;
Barlogie, B ;
Shaughnessy, J .
BLOOD, 2005, 106 (01) :296-303
[9]
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
[10]
Initial genome sequencing and analysis of multiple myeloma [J].
Chapman, Michael A. ;
Lawrence, Michael S. ;
Keats, Jonathan J. ;
Cibulskis, Kristian ;
Sougnez, Carrie ;
Schinzel, Anna C. ;
Harview, Christina L. ;
Brunet, Jean-Philippe ;
Ahmann, Gregory J. ;
Adli, Mazhar ;
Anderson, Kenneth C. ;
Ardlie, Kristin G. ;
Auclair, Daniel ;
Baker, Angela ;
Bergsagel, P. Leif ;
Bernstein, Bradley E. ;
Drier, Yotam ;
Fonseca, Rafael ;
Gabriel, Stacey B. ;
Hofmeister, Craig C. ;
Jagannath, Sundar ;
Jakubowiak, Andrzej J. ;
Krishnan, Amrita ;
Levy, Joan ;
Liefeld, Ted ;
Lonial, Sagar ;
Mahan, Scott ;
Mfuko, Bunmi ;
Monti, Stefano ;
Perkins, Louise M. ;
Onofrio, Robb ;
Pugh, Trevor J. ;
Rajkumar, S. Vincent ;
Ramos, Alex H. ;
Siegel, David S. ;
Sivachenko, Andrey ;
Stewart, A. Keith ;
Trudel, Suzanne ;
Vij, Ravi ;
Voet, Douglas ;
Winckler, Wendy ;
Zimmerman, Todd ;
Carpten, John ;
Trent, Jeff ;
Hahn, William C. ;
Garraway, Levi A. ;
Meyerson, Matthew ;
Lander, Eric S. ;
Getz, Gad ;
Golub, Todd R. .
NATURE, 2011, 471 (7339) :467-472