Table 1.
Characteristic | All patients (n = 122) | ALL (n = 12) | AML (n = 58) | CLL (n = 42) | MPN or MDS/MPN (n = 10) |
Sex (n evaluable) | n = 116 | n = 12 | n = 56 | n = 42 | n = 6 |
Female | 59 | 8 | 30 | 20 | 1 |
Male | 57 | 4 | 26 | 22 | 5 |
Age, y (n evaluable) | n = 106 | n = 9 | n = 54 | n = 37 | n = 6 |
Median | 62.1 | 29.7 | 53.7 | 65.9 | 60.7 |
Range | 5.5–83.8 | 5.5–70.2 | 8.2–83.8 | 44.7–79.4 | 35.2–74.9 |
Sample type (n evaluable) | n = 122 | n = 12 | n = 58 | n = 42 | n = 10 |
Peripheral blood | 86 | 7 | 31 | 41 | 7 |
Bone marrow aspirate | 34 | 5 | 25 | 1 | 3 |
Leukapheresis | 2 | 0 | 2 | 0 | 0 |
WBC count (n evaluable) | n = 115 | n = 9 | n = 55 | n = 42 | n = 9 |
Median, ×1,000/µL | 42.9 | 60.0 | 34.6 | 45.8 | 92.7 |
Range, ×1,000/µL | 0.5–309 | 10.3–169 | 0.5–240 | 5.8–309 | 26.3–240 |
In total, primary samples from 122 patients with a variety of hematologic malignancies were screened for ex vivo sensitivity to inhibitor combinations.