Table 1.
Characteristic | N = 18 |
---|---|
Age, median (range), y | 2.1 (0.3-6.9) |
Time from initial diagnosis to C1D1, median (range), d | 25 (6-80) |
Sex, no. (%) | |
Male | 11 (61) |
Female | 7 (39) |
Somatic mutation/genetic subtype, no. (%) | |
PTPN11 | 13 (72) |
NRAS | 3 (17) |
KRAS | 1 (6) |
NF1 | 1 (6) |
Methylation class, no. (%) | |
High | 11 (61) |
Intermediate | 5 (28) |
Low | 2 (11) |
Karyotype, no. (%) | |
Normal | 12 (67) |
−7 | 3 (17) |
−Y | 1 (6) |
del(9) | 1 (6) |
+21c | 1 (6) |
WBC, median (range), ×109/L | 19.7 (4.3-59.0) |
HbF, median (range) | 18.4 (0.7-59.1) |
Elevated, no. (%) | 15 (83) |
Normal for age, no. (%) | 3 (17) |
Platelet count, median (range), ×109/L | 28 (7-85) |
Patients receiving platelet transfusion, no. (%) | 12* (67) |
Blasts in BM, median (range), % | 6 (0-19) |
Spleen tip palpable below costal margin, median (range), cm | 4 (2-14) |
C, cycle; D, day; WBC, white blood cell.
At C2D1, 16 patients (90%) were platelet transfusion dependent.