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. 2024 Sep 17;38(11):2443–2455. doi: 10.1038/s41375-024-02411-7

Table 1.

Cohort demographics (n = 49).

Characteristic Number (%)/Median [Range]
Age at diagnosis (years) 53.5 [14–80]
Age at Asciminib (years) 59 [23–88]
Gender
Male 27 (55%)
Female 22 (45%)
Disease phase at diagnosis
Chronic 48 (98%)
Accelerated 1 (2%)
Disease phase at asciminib initiation
Chronic 49 (100%)
ACA at diagnosis
No 36 (73%)
Yes 3 (6%)
Unknown 10 (20%)
ELTS score at diagnosis
Low 16 (33%)
Intermediate 9 (18%)
High 4 (8%)
Missing 20 (41%)
Transcript type
e13a2 19 (39%)
e14a2 12 (24%)
e13a2/e14a2 9 (18%)
Unknown, (non-rare) 8 (16%)
e19a2 1 (2%)
Time since diagnosis (months) 73 [11–386]
Number of prior TKIs (median) 4 [2–5]
Last TKI
Imatinib 1 (2%)
Bosutinib 17 (35%)
Dasatinib 5 (10%)
Nilotinib 4 (8%)
Ponatinib 22 (45%)
Prior ponatinib use 29 (59%)
Ponatinib resistant 9 (18%)
Reason for stopping last TKI
Resistance 17 (35%)
Intolerance 32 (65%)
Achieved CCyR to at least 1 previous line of therapy 35 (71%)
BSNV (History)
Any 21 (43%)
T315I 11 (22%)
Non-T315I-BSNV all 12 (24%)
Non-T315I-BSNV clinically significant 10 (20%)

ACA additional chromosomal abnormalities, ELTS Eutos long-term survival, TKI tyrosine kinase inhibitor, CCyR complete cytogenetic response, BSNV, BCR::ABL1 single nucleotide variants.