Table 1.
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.