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. 2024 Feb 2;8(9):2094–2103. doi: 10.1182/bloodadvances.2023011980

Table 1.

Outcomes for patients without FLT3-ITD and those with FLT3-ITDpos according to cooccurring mutation risk groups

Non-FLT3-ITD
FLT3-ITDpos
P value
N %, 95 CI N %, 95 CI
FR mutations
 5-year OS 931 81.5%, 78.9%-83.9% 122 76.9%, 68.1%-83.5% .357
 5-year EFS 931 65.1%, 61.9%-68.1% 122 64.0%, 54.6%-71.9% .547
 5-year relapse risk from EOI1 807 25.3%, 22.3%-28.4% 109 25.5%, 17.6%-34.1% .506
INT risk mutations
 5-year OS 1502 53.2%, 50.6%-55.8% 136 55.9%, 46.8%-63.9% .372
 5-year EFS 1502 38.4%, 35.9%-40.9% 136 41.9%, 33.4%-50.1% .230
 5-year relapse risk from EOI1 1064 47.4%, 44.3%-50.4% 94 41.1%, 30.9%-51.0% .104
PR mutations
 5-year OS 136 49.1%, 40.2%-57.4% 206 38.7%, 31.8%-45.5% .093
 5-year EFS 136 29.7%, 22.1%-37.6% 206 22.2%, 16.7%-28.2% .065
 5-year relapse risk from EOI1 90 53.5%, 42.4%-63.3% 98 59.8%, 49.2%-63.9% .323

Cooccurring mutation risk groups stratified according to favorable (NPM1, CEBPA, RUNX1-RUNX1T1, CBFB-MYH11), poor (WT1, UBTF, NUP98-NSD1), and intermediate (all other) risk mutations.

EOI1, endo of induction 1.