Cytogenetic Alterations in Multiple Myeloma: Prognostic Significance and the Choice of Frontline Therapy

被引:8
|
作者
Stella, Flavia [1 ]
Pedrazzini, Estela [1 ]
Agazzoni, Mara [2 ]
Ballester, Oscar [2 ]
Slavutsky, Irma [1 ]
机构
[1] CONICET Acad Nacl Med, Inst Expt Med, Lab Genet Neoplasias Linfoides, Buenos Aires, DF, Argentina
[2] Acad Nacl Med Buenos Aires, Inst Invest Hematol, Buenos Aires, DF, Argentina
关键词
Cytogenetics; FISH; MGUS; Multiple mieloma; Prognostic factors; Risk groups; Therapy; Thalidomide; Bortezomib; STEM-CELL TRANSPLANTATION; IN-SITU HYBRIDIZATION; COMPARATIVE GENOMIC HYBRIDIZATION; HIGH-DOSE CHEMOTHERAPY; CHROMOSOME BAND 1Q21; P53 GENE DELETION; UNDETERMINED SIGNIFICANCE; INTERGROUPE FRANCOPHONE; MOLECULAR PATHOGENESIS; MONOCLONAL GAMMOPATHY;
D O I
10.3109/07357907.2015.1080833
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Multiple myeloma tumor cells demonstrate multiple and often complex genetic lesions as evaluated by standard cytogenetic/FISH studies. Over the past decade, specific abnormalities have been associated with standard or high-risk clinical behavior and they have become strong prognostic indicators. Further, as evidenced by recent randomized clinical trials, the choice of front-line therapy (transplant vs. no transplant, inclusion of novel drugs such as bortezomib, thalidomide, and lenalidomide) may be able to overcome the adverse effect of high-risk genetic lesions.
引用
收藏
页码:496 / 504
页数:9
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