Disease characteristics at presentation for WM patients stratified by MYD88 and CXCR4 mutation status
. | MYD88WTCXCR4WT . | MYD88L265PCXCR4WT . | MYD88L265PCXCR4WHIM . | P . |
---|---|---|---|---|
n | 15 | 109 | 50 | |
Gender (M/F) | 7/8 | 73/36 | 31/19 | – |
Age (years) | 66 (42-82) | 59 (40-88) | 60 (34-88) | .02 |
BM involvement (%) | 15 (5-65) | 40 (5-95) | 50 (5-95) | .02 |
Abs neutrophil (k/μL) | 2.93 (0.72-3.7) | 3.5 (1.04-8.94) | 3.2 (1.52-8.2) | – |
Abs lymphocyte (k/μL) | 1.61 (0.8-17.3) | 1.73 (0.48-11.1) | 1.69 (0.51-3.98) | .03 |
Hemoglobin (g/dL) | 11.3 (8-14.4) | 11.5 (6-15.5) | 11.6 (4.8-15.6) | – |
Platelet (k/μL) | 218 (105-378) | 274 (75-512) | 251 (42-441) | .01 |
Serum IgA (mg/dL) | 140 (27-324) | 61 (0-1240) | 45 (7-864) | – |
Serum IgG (mg/dL) | 734 (441-1480) | 686 (138-2920) | 595 (168-1330) | – |
Serum IgM (mg/dL) | 2720 (134-5810) | 3190 (345-8720) | 3490 (416-8767) | – |
B2M (mg/L) | 3.1 (2-5.5) | 3.1 (1.4-10.4) | 2.3 (1-9.2) | – |
Adenopathy | 6 (40%) | 59 (54.1%) | 15 (30%) | .01 |
Splenomegaly | 6 (40%) | 18 (16.5%) | 8 (16%) | – |
Family history | 4 (26.7%) | 31(28.4%) | 20 (40%) | – |
Prior MGUS history | 4 (26.7%) | 18 (16.5%) | 8 (16%) | – |
Symptomatic disease | 9 (60%) | 69 (63.3%) | 34 (66.6%) | – |
. | MYD88WTCXCR4WT . | MYD88L265PCXCR4WT . | MYD88L265PCXCR4WHIM . | P . |
---|---|---|---|---|
n | 15 | 109 | 50 | |
Gender (M/F) | 7/8 | 73/36 | 31/19 | – |
Age (years) | 66 (42-82) | 59 (40-88) | 60 (34-88) | .02 |
BM involvement (%) | 15 (5-65) | 40 (5-95) | 50 (5-95) | .02 |
Abs neutrophil (k/μL) | 2.93 (0.72-3.7) | 3.5 (1.04-8.94) | 3.2 (1.52-8.2) | – |
Abs lymphocyte (k/μL) | 1.61 (0.8-17.3) | 1.73 (0.48-11.1) | 1.69 (0.51-3.98) | .03 |
Hemoglobin (g/dL) | 11.3 (8-14.4) | 11.5 (6-15.5) | 11.6 (4.8-15.6) | – |
Platelet (k/μL) | 218 (105-378) | 274 (75-512) | 251 (42-441) | .01 |
Serum IgA (mg/dL) | 140 (27-324) | 61 (0-1240) | 45 (7-864) | – |
Serum IgG (mg/dL) | 734 (441-1480) | 686 (138-2920) | 595 (168-1330) | – |
Serum IgM (mg/dL) | 2720 (134-5810) | 3190 (345-8720) | 3490 (416-8767) | – |
B2M (mg/L) | 3.1 (2-5.5) | 3.1 (1.4-10.4) | 2.3 (1-9.2) | – |
Adenopathy | 6 (40%) | 59 (54.1%) | 15 (30%) | .01 |
Splenomegaly | 6 (40%) | 18 (16.5%) | 8 (16%) | – |
Family history | 4 (26.7%) | 31(28.4%) | 20 (40%) | – |
Prior MGUS history | 4 (26.7%) | 18 (16.5%) | 8 (16%) | – |
Symptomatic disease | 9 (60%) | 69 (63.3%) | 34 (66.6%) | – |
This table denotes comparisons of patient characteristics at diagnosis stratified by all CXCRWHIM-mutated patients.
Abs, absolute; –, not significant.