Table 2. Clinical and laboratory characteristics of 167 patients with essential thrombocythemia according to the mutational status of JAK2 and CALR.
Characteristic | JAK2+/CALR+ (A) | JAK2+/CALR- (B) | JAK2-/CALR+ (C)‡ | JAK2-/CALR- (D) ‡ | P value | |||||
---|---|---|---|---|---|---|---|---|---|---|
AvsB | AvsC | AvsD | BvsC | BvsD | CvsD | |||||
Patients, n (%) | 7 (4) | 103 (62) | 19 (11) | 38 (23) | - | - | - | - | - | - |
Male, n† | 3 | 53 | 10 | 13 | 0.714 | 1.000 | 0.686 | 1.000 | 0.087 | 0.253 |
Age at onset, years, SE (med; ran)* | 7.0(62;29-77) | 1.2(63;6-87) | 3.3(62;25-80) | 2.9(52;11-80) | 0.783 | 0.977 | 0.511 | 0.619 | 0.008 | 0.152 |
WBC count, × 109/L, SE(med; ran)* | 1.5(8.4;3.6–16.9) | 0.7(12.7;5.1–59.6) | 0.8(9.5;4.5–18.8) | 0.5(9.0;4.4–18.3) | 0.006 | 0.355 | 0.594 | 0.002 | <0.0001 | 0.286 |
Hemoglobin, g/dL, SE(med; ran)* | 0.83(13.4;9.6–15.1) | 0.20(13.9;8.4–19.5) | 0.33(13.5;10.1–15.9) | 0.32(12.3;6.6–17.1) | 0.225 | 0.685 | 0.707 | 0.188 | 0.0003 | 0.080 |
Platelet count, × 109/L, SE(med; ran)* | 110(1006;471-1186) | 24(933;487-1935) | 97(1021;557-2232) | 50(998;456-1648) | 0.995 | 0.355 | 0.719 | 0.089 | 0.566 | 0.306 |
Lactate dehydrogenase, mU/mL, SE(med; ran)* | 88(486;185–969) | 19(557;192–1157) | 48(481;200–1000) | 31(462;195–932) | 0.233 | 0.885 | 0.835 | 0.272 | 0.026 | 0.478 |
Splenomegaly, n (%)† | 3 (43) | 35 (34) | 7 (37) | 4 (11) | 0.691 | 1.000 | 0.064 | 0.799 | 0.006 | 0.031 |
Thrombotic events, n (%)† | 0 | 32 (31) | 3 (16) | 3 (8) | 0.104 | 0.540 | 1.000 | 0.270 | 0.004 | 0.389 |
Plateletpheresis, n (%)† | 4 (57) | 34 (33) | 8 (42) | 12 (32) | 0.232 | 0.665 | 0.225 | 0.444 | 1.000 | 0.558 |
Transformation to secondary MF or AL, n (%)† | 0 | 7 (7) | 0 | 0 | 1.000 | N/A | N/A | 0.594 | 0.190 | N/A |
n, number; SE, standard error; med, median; ran, range; WBC, white blood cell; MF, myelofibrosis; AL, acute leukemia; N/A, not applicable.
P values were calculated using the Mann-Whitney U test.
P values were calculated using the Fisher's exact test.
Group C and D were all negative for MPL exon 10 mutation.