Implications of Heterogeneity in Multiple Myeloma

被引:45
|
作者
de Mel, Sanjay [1 ]
Lim, Su Hong [1 ]
Tung, Moon Ley [1 ]
Chng, Wee-Joo [1 ,2 ,3 ]
机构
[1] Natl Univ Singapore, Canc Inst Singapore, Dept Haematol Oncol, Singapore 117548, Singapore
[2] Natl Univ Singapore, Canc Sci Inst Singapore, Singapore 117548, Singapore
[3] Natl Univ Hlth Syst, Singapore 119228, Singapore
关键词
IN-SITU HYBRIDIZATION; INDEPENDENT PROGNOSTIC-FACTOR; MOLECULAR CLASSIFICATION; INTERGROUPE FRANCOPHONE; GENETIC ABNORMALITIES; MONOCLONAL GAMMOPATHY; EXPRESSION SIGNATURE; CHROMOSOME; 1Q21; RAS MUTATIONS; CELL;
D O I
10.1155/2014/232546
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Multiple myeloma is the second most common hematologic malignancy in the world. Despite improvement in outcome, the disease is still incurable for most patients. However, not all myeloma are the same. With the same treatment, some patients can have very long survival whereas others can have very short survival. This suggests that there is underlying heterogeneity in myeloma. Studies over the years have revealed multiple layers of heterogeneity. First, clinical parameters such as age and tumor burden could significantly affect outcome. At the genetic level, there are also significant heterogeneity ranging for chromosome numbers, genetic translocations, and genetic mutations. At the clonal level, there appears to be significant clonal heterogeneity with multiple clones coexisting in the same patient. At the cell differentiation level, there appears to be a hierarchy of clonally related cells that have different clonogenic potential and sensitivity to therapies. These levels of complexities present challenges in terms of treatment and prognostication as well as monitoring of treatment. However, if we can clearly delineate and dissect this heterogeneity, we may also be presented with unique opportunities for precision and personalized treatment of myeloma. Some proof of concepts of such approaches has been demonstrated.
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页数:12
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