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

Table 4.

Comparison between CML-BP as evolution of a chronic phase (secondary BP) and de novo CML-BP.

Variable Secondary CML-BP (N = 151) De novo CML-BP (N = 89)
Patient-related
 Sex, male, n (%) 97 (64.2%) 47 (52.8%)
 Age at onset of CML-BP (yrs), median (range) 49 (18–85) 48 (20–86)
CML-related
 Morphology of CML-BP, n/N (%) Myeloid 75/148 (50.7%) 42/85 (49.4%)
Lymphoid 46/148 (31.1%) 25/85 (29.4%)
Mixed 5/148 (3.4%) 5/85 (5.9%)
Megakaryoblastic 1/148 (0.7%) 2/85 (2.4%)
Unknown 21/148 (14.2%) 11/85 (12.9%)
Not reported 3 (2.0%) 4 (4.5%)
 Additional chromosomal abnormalities (ACAs), yes, n/N(%) Complex karyotype 38/101 (37.6%) 14/73 (19.2%)
Chr. 3q26.2 rearrangements 6/101 (5.9%) 3/73 (4.1%)
−7/−7q 12/101 (11.9%) 0/73 (0%)
+8 23/101 (22.8%) 0/73 (0%)
others 41/101 (40.6%) 22/73 (30.1%)
Not reported 50 (33.1%) 16 (18.0%)
 High risk ACAsa, yes, n/N(%) 56/101 (55.4%) 16/73 (21.9%)
Not reported 50 (33.1%) 16 (18.0%)
 Mutations in BCR::ABL1, yes, n/N(%) 39/104 (37.5%) 7/62 (11.3%)
Not reported 47 (31.1%) 27 (30.3%)
 CNS involvement, yes, n/N(%) 10/133 (7.5%) 11/81 (13.6%)
Not reported 18 (11.9%) 8 (9.0%)
 Extramedullary disease, yes, n/N(%) 27/136 (19.9%) 16/84 (19.0%)
Not reported 15 (9.9%) 5 (5.6%)

CML-BP chronic myeloid leukemia blast phase, M male, F female, yrs years, 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.