The Impact of Genomics on the Management of Myeloma

被引:9
作者
Corre, Jill [1 ]
Avet-Loiseau, Herve [2 ]
机构
[1] Ctr Hosp Univ Toulouse, UMR 1037, Toulouse, France
[2] Ctr Hosp Univ Nantes, INSERM, U892, Nantes, France
来源
JOURNAL OF THE NATIONAL COMPREHENSIVE CANCER NETWORK | 2011年 / 9卷 / 10期
关键词
Myeloma; genomics; prognosis; STEM-CELL TRANSPLANTATION; IN-SITU HYBRIDIZATION; ADVERSE PROGNOSTIC-FACTOR; P53 GENE DELETION; MULTIPLE-MYELOMA; MOLECULAR CLASSIFICATION; INTERGROUPE FRANCOPHONE; EXPRESSION; T(4/14); ABNORMALITIES;
D O I
10.6004/jnccn.2011.0097
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Myeloma is a complex disease, characterized by a wide heterogeneity in clinical presentation, evolution, and molecular portraits. The successive use of cytogenetics, molecular cytogenetics, expression genomics, copy number genomics, and, more recently, deep sequencing, has shown that this heterogeneity can be used to identify markers usable for not only prognostication but also therapeutic choice and, ultimately, discovery of druggable targets. The use of some of these techniques is now mandatory for the management of patients. Although risk-adapted therapy is not yet a routine practice in myeloma, these molecular changes are essential for the definition of the prognosis. (JNCCN 2011;9:1200-1207)
引用
收藏
页码:1200 / 1206
页数:7
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