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Revised primary molecular cytogenetic classification of myeloma

Revised primary molecular cytogenetic classification of myeloma
FISH abnormality Percentage of myeloma patients
Trisomy(ies) without IgH abnormality 42
IgH abnormality without trisomy(ies) 30
t(11;14) 15
t(4;14) 6
t(14;16) 4
t(14;20) <1
Unknown partner/deletion of IgH region 5
IgH abnormality with trisomy(ies) 15
t(11;14) 3
t(4;14) 4
t(14;16) 1
t(6;14) <1
Unknown partner/deletion of IgH region 7
Monosomy 14 in absence of IgH translocations or trisomy(ies) 4.5
Other cytogenetic abnormalities in absence of IgH translocations or trisomy(ies) or monosomy 14* 5.5
Normal 3
The table describes the distribution of various abnormalities detected by fluorescent in situ hybridization (FISH) in a population of 484 patients with newly diagnosed symptomatic multiple myeloma.
* These included primarily monosomy 13 and p53 abnormalities.
This research was originally published in Blood. Kumar S, Fonseca R, Ketterling RP, et al. Trisomies in multiple myeloma: impact on survival in patients with high-risk cytogenetics. Blood 2012; 119:2100. Copyright © 2012 American Society of Hematology.
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