Table 1

Characteristics of the 83 maB-NHLs analyzed in the present study (detailed information is shown in Table S1)

Molecular diagnosisAge, y: median (min-max)Sex, F/MMorphology: BL/aBL/DLBCL/agNHLt(MYC): yes/noIGH/BCL2: yes/noImbalances*: median (min-max)
Total, n = 83 60 (2-90) 32/51 (39%/61%) 5/12/60/6 (6%/14%/72%/7%) 26/57 (31%/69%) 10/73 (12%/88%) 7 (0-25) 
mBL, n = 18 13 (2-63) 6/12 (33%/67%) 5/10/2/1 (28%/56%/11%/6%) 18/0 (100%/0%) 0/18 (0%/100%) 2 (0-17) 
Non-mBL, n = 49 66 (18-88) 19/30 (39%/61%) 0/0/46/3 (0%/0%/94%/6%) 2/47 (4%/96%) 6/43 (12%/88%) 9 (0-22) 
    ABC, n = 29 67 (41-88) 10/19 (34%/66%) 0/0/28/1 (0%/0%/97%/3%) 1/28 (3%/97%) 0/29 (0%/100%) 9.5 (3-22) 
    GCB, n = 20 62 (18-85) 9/11 (45%/55%) 0/0/18/2 (0%/0%/90%/10%) 1/19 (5%/95%) 6/14 (30%/70%) 7.5 (0-16) 
Intermediate, n = 16 56 (4-90) 7/9 (44%/56%) 0/2/12/2 (0%/13%/75%/13%) 6/10 (38%/63%) 4/12 (25%/75%) 8.5 (0-25) 
Molecular diagnosisAge, y: median (min-max)Sex, F/MMorphology: BL/aBL/DLBCL/agNHLt(MYC): yes/noIGH/BCL2: yes/noImbalances*: median (min-max)
Total, n = 83 60 (2-90) 32/51 (39%/61%) 5/12/60/6 (6%/14%/72%/7%) 26/57 (31%/69%) 10/73 (12%/88%) 7 (0-25) 
mBL, n = 18 13 (2-63) 6/12 (33%/67%) 5/10/2/1 (28%/56%/11%/6%) 18/0 (100%/0%) 0/18 (0%/100%) 2 (0-17) 
Non-mBL, n = 49 66 (18-88) 19/30 (39%/61%) 0/0/46/3 (0%/0%/94%/6%) 2/47 (4%/96%) 6/43 (12%/88%) 9 (0-22) 
    ABC, n = 29 67 (41-88) 10/19 (34%/66%) 0/0/28/1 (0%/0%/97%/3%) 1/28 (3%/97%) 0/29 (0%/100%) 9.5 (3-22) 
    GCB, n = 20 62 (18-85) 9/11 (45%/55%) 0/0/18/2 (0%/0%/90%/10%) 1/19 (5%/95%) 6/14 (30%/70%) 7.5 (0-16) 
Intermediate, n = 16 56 (4-90) 7/9 (44%/56%) 0/2/12/2 (0%/13%/75%/13%) 6/10 (38%/63%) 4/12 (25%/75%) 8.5 (0-25) 

mBL indicates molecular Burkitt lymphoma; ABC, activated B cell; GCB, germinal center B cell; F, female; M, male; BL, Burkitt lymphoma; aBL, atypical BL; DLBCL, diffuse large B-cell lymphoma; agNHL, aggressive B-NHL unclassifiable; t(MYC), translocation affecting the MYC locus; and IGH/BCL2, fusion of the IGH and BCL2 loci as a result of a translocation t(14;18)(q32;q21).

*

Defined as number of chromosomal imbalances detected by array comparative genomic hybridization (CGH).17 

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