Table 2.

Frequency of cytogenetic iFISH aberrations depending on disease (PC-AL vs PC–non-AL) and stage of plasma cell dyscrasia (MGUS/SMM/MM)

PC-ALPC–non-ALP (PC-AL vs PC–non-AL)
n/N (%)Pn/N (%)P
Total (n = 544)MGUS (n = 164)SMM (n = 345)MM (n = 35)Total (n = 519)MGUS (n = 62)SMM (n = 156)MM (n = 301)
Translocations            
 t(11;14) 331/544 (60.8) 117/164 (71.3) 200/345 (58.0) 14/35 (40.0) .001 76/519 (14.6) 4/62 (6.5) 7/156 (4.5) 65/301 (21.6) <.001 <.001 
 t(4;14) 19/544 (3.5) 1/164 (0.6) 16/345 (4.6) 2/35 (5.7) .17 86/519 (16.6) 6/62 (9.7) 33/156 (21.2) 47/301 (15.6) .81 <.001 
 t(14;16) 13/543 (2.4) 2/164 (1.2) 11/344 (3.2) 0/35 (0) .58 30/511 (5.5) 9/60 (15.0) 15/153 (9.8) 6/298 (2.0) <.001 <.001 
 IgH unknown 94/541 (17.4) 25/164 (15.2) 286/343 (16.6) 12/34 (35.3) .25 166/489 (33.9) 37/61 (60.7) 75/153 (49.0) 54/275 (19.6) <.001 <.001 
Gains            
 1q21 167/544 (30.7) 40/164 (24.4) 115/345 (33.3) 12/35 (34.3) .25 195/519 (37.6) 23/62 (37.1) 69/156 (44.2) 103/301 (34.2) .75 .034 
 5p15/5q35 83/533 (15.6) 17/160 (10.6) 54/341 (15.8) 12/32 (37.5) .013 136/367 (37.1) 17/54 (31.5) 54/148 (36.5) 65/165 (39.4) .75 <.001 
 9q34 172/543 (31.7) 42/163 (25.8) 112/345 (32.5) 18/35 (51.4) .054 283/517 (54.7) 31/62 (50.0) 80/156 (51.3) 172/299 (57.5) .75 <.001 
 11q22.3 211/544 (38.8) 71/164 (43.3) 128/345 (37.1) 12/35 (34.3) .31 224/519 (43.2) 15/62 (24.2) 58/156 (37.2) 151/301 (50.2) <.001 .59 
 11q23 
 15q22 97/544 (17.9) 19/163 (11.7) 64/344 (18.6) 14/35 (40.0) .004 245/517 (47.5) 21/62 (33.9) 65/156 (41.7) 159/299 (53.2) .01 <.001 
 19q13 102/542 (18.8) 21/163 (12.9) 70/344 (20.3) 11/35 (31.4) .054 258/519 (49.7) 23/62 (37.1) 73/156 (46.8) 162/301 (53.8) .067 <.001 
Deletions            
 8p21 38/534 (7.1) 6/161 (3.7) 28/338 (8.3) 4/35 (11.4) .22 108/519 (20.8) 3/62 (4.8) 29/156 (18.6) 76/301 (25.2) .003 .034 
 13q14 209/544 (38.4) 56/164 (34.1) 133/345 (38.6) 20/35 (57.1) .22 264/519 (50.9) 2 /62 (41.9) 79/156 (50.6) 159/301 (52.8) .75 .071 
 17p13 16/544 (2.9) 3/164 (1.8) 10/345 (2.9) 3/35 (8.6) .25 47/519 (9.1) 1/62 (1.6) 10/156 (6.4) 36/301 (12.0) .024 .19 
PC-ALPC–non-ALP (PC-AL vs PC–non-AL)
n/N (%)Pn/N (%)P
Total (n = 544)MGUS (n = 164)SMM (n = 345)MM (n = 35)Total (n = 519)MGUS (n = 62)SMM (n = 156)MM (n = 301)
Translocations            
 t(11;14) 331/544 (60.8) 117/164 (71.3) 200/345 (58.0) 14/35 (40.0) .001 76/519 (14.6) 4/62 (6.5) 7/156 (4.5) 65/301 (21.6) <.001 <.001 
 t(4;14) 19/544 (3.5) 1/164 (0.6) 16/345 (4.6) 2/35 (5.7) .17 86/519 (16.6) 6/62 (9.7) 33/156 (21.2) 47/301 (15.6) .81 <.001 
 t(14;16) 13/543 (2.4) 2/164 (1.2) 11/344 (3.2) 0/35 (0) .58 30/511 (5.5) 9/60 (15.0) 15/153 (9.8) 6/298 (2.0) <.001 <.001 
 IgH unknown 94/541 (17.4) 25/164 (15.2) 286/343 (16.6) 12/34 (35.3) .25 166/489 (33.9) 37/61 (60.7) 75/153 (49.0) 54/275 (19.6) <.001 <.001 
Gains            
 1q21 167/544 (30.7) 40/164 (24.4) 115/345 (33.3) 12/35 (34.3) .25 195/519 (37.6) 23/62 (37.1) 69/156 (44.2) 103/301 (34.2) .75 .034 
 5p15/5q35 83/533 (15.6) 17/160 (10.6) 54/341 (15.8) 12/32 (37.5) .013 136/367 (37.1) 17/54 (31.5) 54/148 (36.5) 65/165 (39.4) .75 <.001 
 9q34 172/543 (31.7) 42/163 (25.8) 112/345 (32.5) 18/35 (51.4) .054 283/517 (54.7) 31/62 (50.0) 80/156 (51.3) 172/299 (57.5) .75 <.001 
 11q22.3 211/544 (38.8) 71/164 (43.3) 128/345 (37.1) 12/35 (34.3) .31 224/519 (43.2) 15/62 (24.2) 58/156 (37.2) 151/301 (50.2) <.001 .59 
 11q23 
 15q22 97/544 (17.9) 19/163 (11.7) 64/344 (18.6) 14/35 (40.0) .004 245/517 (47.5) 21/62 (33.9) 65/156 (41.7) 159/299 (53.2) .01 <.001 
 19q13 102/542 (18.8) 21/163 (12.9) 70/344 (20.3) 11/35 (31.4) .054 258/519 (49.7) 23/62 (37.1) 73/156 (46.8) 162/301 (53.8) .067 <.001 
Deletions            
 8p21 38/534 (7.1) 6/161 (3.7) 28/338 (8.3) 4/35 (11.4) .22 108/519 (20.8) 3/62 (4.8) 29/156 (18.6) 76/301 (25.2) .003 .034 
 13q14 209/544 (38.4) 56/164 (34.1) 133/345 (38.6) 20/35 (57.1) .22 264/519 (50.9) 2 /62 (41.9) 79/156 (50.6) 159/301 (52.8) .75 .071 
 17p13 16/544 (2.9) 3/164 (1.8) 10/345 (2.9) 3/35 (8.6) .25 47/519 (9.1) 1/62 (1.6) 10/156 (6.4) 36/301 (12.0) .024 .19 

Frequency of cytogenetic aberrations in the AL amyloidosis group (PC-AL) as compared with the MGUS/SMM/MM control group (PC–non-AL group). Frequencies are also detailed for the respective stages of plasma cell dyscrasia. P values indicate changes of the frequency of the respective aberrations depending on the stage of plasma cell dyscrasia. The P value in the last column addresses the frequency difference between the PC-AL and PC–non-AL groupS (adjusted for the respective frequencies of MGUS/SMM/MM in both groups via logistic regression). All P values were adjusted for multiple testing across probes using Holm correction to control the family-wise error rate.

Close Modal

or Create an Account

Close Modal
Close Modal