Figure 3
Figure 3. OS and RFS stratified by proposed scoring system. Kaplan-Meier survival curves for OS (A) and RFS (B) in AML patients based on our new scoring system (P < .001 for both OS and RFS). AML patients were grouped according to our scoring system based on the DNMT3A mutation and 8 other prognostic markers (ie, age, WBC count at diagnosis, and CEBPAdouble-mutation, NPM1/FLT3-ITD, IDH2, DNMT3A, WT1, and AML1/RUNX1 mutations). A score of βˆ’1 was assigned for each parameter associated with a favorable outcome (ie, CEBPAdouble-mutation, IDH2 mutation, and NPM1+/FLT3-ITDβˆ’); a score of +1 was assigned for each factor associated with an adverse outcome (ie, older age, higher WBC counts at diagnosis, and DNMT3A, WT1, and AML1/RUNX1 mutations). The karyotypes were stratified into 3 groups (+2, unfavorable; +1, intermediate; and 0, favorable). The algebraic summation of these scores for each patient was the final score. The 12 patients without chromosome data were not included in the analysis.

OS and RFS stratified by proposed scoring system. Kaplan-Meier survival curves for OS (A) and RFS (B) in AML patients based on our new scoring system (P < .001 for both OS and RFS). AML patients were grouped according to our scoring system based on the DNMT3A mutation and 8 other prognostic markers (ie, age, WBC count at diagnosis, and CEBPAdouble-mutation, NPM1/FLT3-ITD, IDH2, DNMT3A, WT1, and AML1/RUNX1 mutations). A score of βˆ’1 was assigned for each parameter associated with a favorable outcome (ie, CEBPAdouble-mutation, IDH2 mutation, and NPM1+/FLT3-ITDβˆ’); a score of +1 was assigned for each factor associated with an adverse outcome (ie, older age, higher WBC counts at diagnosis, and DNMT3A, WT1, and AML1/RUNX1 mutations). The karyotypes were stratified into 3 groups (+2, unfavorable; +1, intermediate; and 0, favorable). The algebraic summation of these scores for each patient was the final score. The 12 patients without chromosome data were not included in the analysis.

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