Skip to main content
. 2024 Mar 28;38(5):1072–1080. doi: 10.1038/s41375-024-02204-y

Table 1.

Patients and disease characteristics.

Variable N
Patient-related
 Sex, male, n (%) 240 144 (60.0%)
 Age at CML diagnosis (yrs), median (range) 240 45 (13–86)
 Age at onset of CML-BP (yrs), median (range) 240 49 (18–86)
 Phase at diagnosis, n (%) CML-CP 240 151 (62.9%)
CML-BP 89 (37.0%)
 Onset of CML-BP after diagnosis of CML-CP (mo), median (range) 151 29.1 (0.1–378)
 ELTS Score at diagnosis of CML-CP, n (%) Low risk, n (%) 151 36 (39.6%)
Intermediate risk, n (%) 33 (36.3%)
High risk, n (%) 22 (24.2%)
CML-related
 Morphology of CML-BP Myeloid 233 117 (50.2%)
Lymphoid 71 (30.5%)
Mixed 10 (4.3%)
Megakaryoblastic 3 (1.3%)
Unknown 32 (13.7%)
Not reported 7
 Additional chromosomal abnormalities (ACAs) at onset of CML-BP, yes, n (%) Complex karyotype 174 52 (29.9%)
Chr. 3q26.2 rearrangements 9 (5.2%)
−7/−7q 12 (6.9%)
+8 23 (13.2%)
+Ph 20 (11.5%)
Others 50 (28.7%)
Not reported 66
 High risk ACAsa, yes, n (%) 174 72 (41.4%)
Not reported 66
 CNS involvement, yes, n (%) 214 21 (9.8%)
Not reported 26
 Extramedullary disease, yes, n (%) 220 43 (19.5%)
Not reported 20

M male, F female, CML chronic myeloid leukemia, yrs years, CML-BP chronic myeloid leukemia blast phase, CML-CP chronic myeloid leukemia chronic phase, mo months, ELTS EUTOS long term survival, chr. chromosome, CNS central nervous system.

aHigh risk ACAs: +8, +Ph, i[17q], +17, +19, +21, 11q23 and 3q26.2 rearrangements, −7/−7q abnormalities, complex karyotype.