Table 1.
Variables | All patients (n = 10) |
---|---|
Age in years at diagnosis; median (range) | 63 (50–83) |
Females, n (%) | 6 (60) |
Leukocytes × 109/L; median (range) | 58 (19.3–175) |
Absolute monocyte count × 109/L; median (range) | 7 (0.8–29.6) |
Blood monocyte %; median (range) | 12 (3–21) |
Absolute eosinophil count × 109/L; median (range) | 0.8 (0.3–8.4) |
Blood eosinophil %; median (range) | 2 (1–7) |
Absolute basophil count × 109/L; median (range) | 0.9 (0.06-4.2) |
Blood basophil %; median (range) | 2.5 (0.46-5) |
Absolute myelocyte count × 109/L; median (range) | 3.3 (0-29.7) |
Blood myelocyte %; median (range) | 5.5 (0-3) |
Blood blast count × 109/L; median (range) | 0.9 (0-4) |
Blood blast %; median (range) | 1 (0-2) |
Bone marrow blast %; median (range) | 1 (0–2) |
Bone marrow reticulin fibrosis grade; median (range) | 0 (0-1) |
Hemoglobin g/dL; median (range) | 12.5 (10–14.4) |
Platelets × 109/L; median (range) | 209 (118–479) |
Philadelphia chromosome karyotype at time of diagnosis, n (%) | 100% |
No. of metaphases analyzed; median (range) | 20 (20–25) |
Metaphases involved, (n) | |
100% | 7 |
80% | 1 |
35% | 2 |
Palpable splenomegaly, n (%) | 2 (20) |
Symptoms at time of diagnosis seen in 2 or more patients: | |
Asymptomatic, n (%) | 5 (50) |
Fatigue, n (%) | 3 (30) |
Abdominal discomfort, n (%) | 2 (20) |
Tyrosine Kinase Inhibitor response at any time: | |
Complete hematologic response (CHR), n (%) | 10 (100) |
Complete cytogenetic response (CCyR), n (%) | 8 (80) |
Major molecular response (MMR), n (%) | 5 (50) |
Follow-up period from diagnosis in years; median (range) | 6 (1–16) |
Deaths, n (%) Both deaths were unrelated to CML |
2 (20) |
Progression to Acute Myeloid Leukemia, n (%) | 0 (0) |
Allogeneic hematopoietic stem cell transplant, n (%) | 0 (0) |