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. 2023 May 23;30(6):5214–5226. doi: 10.3390/curroncol30060396

Table 3.

Cytogenetics at diagnosis.

Studies without a Comparator Studies with a Comparator
Shin
2017 [10]
Jurczyszyn
2019 [13]
Pál
2020
[14,15]
Duek
2021
[15]
Caulier
2021 [16]
Pydi
2021 [22]
Bao
2022 [17] h
Ludwig
2008 [9]
Jurczyszyn
2016 [19]
Lu
2016 [18]
Nakaya
2020 [21]
Age studied
(years)
≤40 ≤30 ≤40 <50 ≤40 ≤40 <50 <50 ≥50 21–40 41–60 <50 ≥50 <40 years All patients
Median 74
Hyperdiploid NA NA 6/11 (55) 1/22
(4.5)
NA NA NA NA NA NA NA 3/33 (9) 8/120 (7) NA NA
Non-hyperdiploid NA 19/21 (90) NA NA NA NA Hypodiploid
5/210 (2)
NA NA NA NA 4/33 (12) 24/120 (20) NA NA
t(11;14) NA 1/20 (5) NA 15/22 (68) a,b 9/35 (26) 2/7 (29) 42/210 (20) NA NA NA NA NA NA 1/5 (20) 83/316 (26)
p = 0.461
t(14;16) 0/11 (0) NA NA 0/22 (0) 1/39 (2.5) 1/7 (14) NA NA NA NA NA NA NA 0/7 (0) 27/532 (5)
p = 0.063
t(14;20) 0/6 (0) NA NA 0/22 (0) NA NA NA NA NA NA NA NA NA NA NA
t(8;14) NA NA NA NA NA NA 4/210 (2) NA NA NA NA NA NA NA NA
t(4;14) 1/10 (10) 0/20 (0) 3/11 (27) 0/22 (0) 19/156 (12) e 1/7 (14) 15/210 (7) NA NA 26/81 (32) j 31/181 (17) j
p = 0.007
NA NA 2/8 (25) 168/802 (21)
p = 0.659
del (17p)/17
delp53
1/9 (11) 2/21 (10) 2/11 (18) 1/22 (4.5) 17/141 (12) e 1/7 (14) 15/210 (7) NA NA 17/91 (19) i 61/351 (17)
p 0.771 i
3/9 (33) 86/606 (14)
p = 0.008
+ or amp 1q21/1q gain 4/15 (27) 2/17 (12) NA NA 17/56 (30) f NA 48/210 (23) NA NA NA NA 49/87 (56) i 139/313
(44)
p = 0.064 i
NA NA
del (1p32) NA NA NA 1/22 (4.5) c 8/46 (17) g NA NA NA NA NA NA NA NA NA NA
del (13q)/
del 13
4/17 (24) 8/26 (31) NA 9/22 (40) d NA 3/7 (43) 72/210 (34) 32/53 (60) i 150/320 (47)
p = 0.069 i
NA NA 13/37 (35) i 58/141 (41)
p = 0.507 i
4/8 (50) 211/435 (49)
p = 1.000
17/109 (16) ii 45/345 (13)
p = 0.499 ii
3/33 (9) ii 9/120 (8)
p = 0.767 ii
del (9) 1/16 (6) NA NA NA NA NA NA NA NA NA NA NA NA NA NA

NA: not available. a sole aberration in 32%; b 3 also had IgH rearrangement, 6 also had del 13q, 1 also had delp53; c 1 also IgH rearranged; d 1 also had delp53, 6 also t(11;14), 3 also IgH rearranged, 1 also del 16q; e 2 patients had t(4;14) and del (17p); f Associated with high-risk cytogenetics in 5 patients; g Associated with high-risk cytogenetics in 2 patients and associated with +1q in 5 patients; h 7% had ≥2 high-risk chromosomal abnormalities; i by FISH; ii by conventional cytogenetics; j del (17p) and t(4;14) merged. Numbers in parentheses represent percentages.