Treatment options based on dominant AML mutations

Dominant mutationAvailable target agentAvailable therapeutic regimensTherapeutic impact
FLT3-ITD or TKD Midostaurin In combination with “7 + 3” Incremental improvement in survival 
 Gilteritinib Single-agent therapy in relapse Single-agent response rate of 34%8  
  In combination with higher doses of cytarabine Higher response rate in combination9  
  In combination with hypomethylating agents  
 Quizartinib Single-agent maintenance; single-agent therapy in relapse; combination therapy at diagnosis  
IDH1 Ivosidenib Single agent OR in combination with “7 + 3” OR in combination with hypomethylating agents at diagnosis Response rate with hypomethylating agents in newly diagnosed AML was 47%, and 1-y event-free survival was 37%10  
IDH2 Enasidenib Single agent in relapse Median overall survival in relapsed setting was 6.5 mo11  
Dominant mutationAvailable target agentAvailable therapeutic regimensTherapeutic impact
FLT3-ITD or TKD Midostaurin In combination with “7 + 3” Incremental improvement in survival 
 Gilteritinib Single-agent therapy in relapse Single-agent response rate of 34%8  
  In combination with higher doses of cytarabine Higher response rate in combination9  
  In combination with hypomethylating agents  
 Quizartinib Single-agent maintenance; single-agent therapy in relapse; combination therapy at diagnosis  
IDH1 Ivosidenib Single agent OR in combination with “7 + 3” OR in combination with hypomethylating agents at diagnosis Response rate with hypomethylating agents in newly diagnosed AML was 47%, and 1-y event-free survival was 37%10  
IDH2 Enasidenib Single agent in relapse Median overall survival in relapsed setting was 6.5 mo11  
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