Table 2

Frequency of cytogenetic aberrations

FISH cytogenetic aberrationsTransplant group (n = 123)Drop-out group (n = 17)
No.*%No.*%
IgH translocations     
 t(11;14) 72/123 59 9/17 53 
 t(4;14) 5/123 0/16 
 t(14;16) 1/122 1/16 
 IgH translocation with unknown partner 20/12 1 17 2/16 13 
Gain     
 1q21 25/116 22 2/16 13 
 5p15/5q35 9/110 0/15 
 9q34 25/112 22 0/15 
 15q22 16/110 15 0/15 
 19q13 16/114 14 0/16 
Deletion     
 13q14 36/123 29 5/16 31 
 17p13 3/123 0/16 
Hyperdiploidy 16/111 14 0/15 
High-risk aberrations§ 9/122 1/16 
Normal iFISH, no aberration detected 7/123 3/17 18 
FISH cytogenetic aberrationsTransplant group (n = 123)Drop-out group (n = 17)
No.*%No.*%
IgH translocations     
 t(11;14) 72/123 59 9/17 53 
 t(4;14) 5/123 0/16 
 t(14;16) 1/122 1/16 
 IgH translocation with unknown partner 20/12 1 17 2/16 13 
Gain     
 1q21 25/116 22 2/16 13 
 5p15/5q35 9/110 0/15 
 9q34 25/112 22 0/15 
 15q22 16/110 15 0/15 
 19q13 16/114 14 0/16 
Deletion     
 13q14 36/123 29 5/16 31 
 17p13 3/123 0/16 
Hyperdiploidy 16/111 14 0/15 
High-risk aberrations§ 9/122 1/16 
Normal iFISH, no aberration detected 7/123 3/17 18 

IgH, immunoglobulin H.

*

Frequencies (no./N) of the respective cytogenetic aberrations are shown.

Refers to the patients initially deemed eligible for HDM who could not proceed to HDM as a result of TRM, AL progression, or treatment toxicity during the induction or the mobilization phase or because they were unable to mobilize stem cells.

Hyperdiploidy is defined as trisomies of least 2 of the 3 loci (5p15/5q35, 9q34, and 15q22), according to Wuilleme et al.26 

§

High-risk aberrations are defined by the detection of t(4;14), t(14;16), or del(17p13).18 

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