Staging and prognostication of multiple myeloma

被引:30
作者
Fonseca, Rafael [1 ,2 ]
Monge, Jorge [2 ]
Dimopoulos, Meletios A. [3 ]
机构
[1] Mayo Clin, Dept Med, Scottsdale, AZ 85259 USA
[2] Mayo Clin, Div Hematol & Oncol, Scottsdale, AZ 85259 USA
[3] Univ Athens, Sch Med, Dept Clin Therapeut, GR-11527 Athens, Greece
关键词
cytogenetics; gene expression profiling; genetics; induction; maintenance; multiple myeloma; prognosis; risk stratification; stem cell transplant; STEM-CELL TRANSPLANTATION; IN-SITU HYBRIDIZATION; UNDETERMINED SIGNIFICANCE MGUS; BORTEZOMIB-THALIDOMIDE-DEXAMETHASONE; GENE-EXPRESSION PROFILES; HIGH-RISK CYTOGENETICS; MARROW PLASMA-CELLS; MONOCLONAL GAMMOPATHY; MOLECULAR CLASSIFICATION; IGH TRANSLOCATIONS;
D O I
10.1586/17474086.2014.882224
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Multiple myeloma (MM) is a heterogeneous disease that, over the past 15 years, has seen an increased understanding of its biology and of novel therapeutic options. Distinctive subtypes of the disease have been described, each with different outcomes and clinic-pathological features. Even though a detailed classification of MM into at least seven or eight major subtypes is possible, a more practical clinical approach can classify the disease into high-risk and non-high-risk MM. Such classification has permitted a more personalized approach to the management of the disease. Additionally, risk stratification should be included in outcome discussions with patients, as survival differs significantly by high-risk status. Nowadays, test for risk stratification are widely available and can be routinely used in the clinic. A greater understanding of the genetic abnormalities underlying the biology of MM will allow for the development of novel targeted therapies and better prognostic markers of the disease.
引用
收藏
页码:21 / 31
页数:11
相关论文
共 120 条
[1]   Absence of p53 deletions in bone marrow plasma cells of patients with monoclonal gammopathy of undedetermined significance [J].
Ackermann, J ;
Meidlinger, P ;
Zojer, N ;
Gisslinger, H ;
Ludwig, H ;
Huber, H ;
Drach, J .
BRITISH JOURNAL OF HAEMATOLOGY, 1998, 103 (04) :1161-1163
[2]   Upregulation of translational machinery and distinct genetic subgroups characterise hyperdiploidy in multiple myeloma [J].
Agnelli, Luca ;
Fabris, Sonia ;
Bicciato, Silvio ;
Basso, Dario ;
Baldini, Luca ;
Morabito, Fortunato ;
Verdelli, Donata ;
Todoerti, Katia ;
Lambertenghi-Deliliers, Giorgio ;
Lombardi, Luigia ;
Neri, Antonino .
BRITISH JOURNAL OF HAEMATOLOGY, 2007, 136 (04) :565-573
[3]   Gene Expression Profiles of Tumor Biology Provide a Novel Approach to Prognosis and May Guide the Selection of Therapeutic Targets in Multiple Myeloma [J].
Anguiano, Ariel ;
Tuchman, Sascha A. ;
Acharya, Chaitanya ;
Salter, Kelly ;
Gasparetto, Cristina ;
Zhan, Fenghuang ;
Dhodapkar, Madhav ;
Nevins, Joseph ;
Barlogie, Bart ;
Shaughnessy, John D., Jr. ;
Potti, Anil .
JOURNAL OF CLINICAL ONCOLOGY, 2009, 27 (25) :4197-4203
[4]  
[Anonymous], BLOOD
[5]   Lenalidomide Maintenance after Stem-Cell Transplantation for Multiple Myeloma [J].
Attal, Michel ;
Lauwers-Cances, Valerie ;
Marit, Gerald ;
Caillot, Denis ;
Moreau, Philippe ;
Facon, Thierry ;
Stoppa, Anne Marie ;
Hulin, Cyrille ;
Benboubker, Lofti ;
Garderet, Laurent ;
Decaux, Olivier ;
Leyvraz, Serge ;
Vekemans, Marie-Christiane ;
Voillat, Laurent ;
Michallet, Mauricette ;
Pegourie, Brigitte ;
Dumontet, Charles ;
Roussel, Murielle ;
Leleu, Xavier ;
Mathiot, Claire ;
Payen, Catherine ;
Avet-Loiseau, Herve ;
Harousseau, Jean-Luc .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (19) :1782-1791
[6]  
Avet-Loiseau H, 1999, CANCER RES, V59, P4546
[7]   Combining fluorescent in situ hybridization data with ISS staging improves risk assessment in myeloma: an International Myeloma Working Group collaborative project [J].
Avet-Loiseau, H. ;
Durie, B. G. M. ;
Cavo, M. ;
Attal, M. ;
Gutierrez, N. ;
Haessler, J. ;
Goldschmidt, H. ;
Hajek, R. ;
Lee, J. H. ;
Sezer, O. ;
Barlogie, B. ;
Crowley, J. ;
Fonseca, R. ;
Testoni, N. ;
Ross, F. ;
Rajkumar, S. V. ;
Sonneveld, P. ;
Lahuerta, J. ;
Moreau, P. ;
Morgan, G. .
LEUKEMIA, 2013, 27 (03) :711-717
[8]   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
[9]   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
[10]  
Avet-Loiseau H, 2010, BLOOD, V117, P2009