Table 5.
Roadmap of AML treatments
| ND AML | IC candidate | FLT3 mutation | 
 7 + 3 + midostaurin Clinical trial: 7 + 3 + midostaurin vs 7 + 3 + gilteritinib  | 
| Low, Intermediate risk (CD33 +) | 7 + 3 + GO | ||
| Secondary AML | CPX351 | ||
| IDH1/2 mutation | 7 + 3 or clinical trial | ||
| No targetable Mutation | Clinical trial or 7 + 3 like regimens | ||
| TP53 mutation | Clinical trial or HMA-based regimens | ||
| Not IC candidate | IDH1/IDH2 mutation | 
 Clinical trial HMA + venetoclax LDAC + venetoclax AZA + IDH inhibitor  | 
|
| FLT3 mutation | 
 Clinical trial HMA + venetoclax LDAC + venetoclax HMA + gilteritinib  | 
||
| No mutation | 
 Clinical trial HMA + venetoclax LDAC + venetoclax  | 
||
| TP53 mutation | 
 Clinical trails AZA + magrolimab AZA + APR-246 Off trial: HMA + venetoclax LDAC + venetoclax 5 day or 10 day Decitabine  | 
||
| R/R AML | IC candidate | Re-induction best on the clinical trial | |
| CD33 + | Clinical trials or GO based regimens, | ||
| IDH1/2 mutation | 
 Ivosidenib/enasidenib alone or HMA combination Venetoclax-based combinations (2 drugs or 3 drugs)  | 
||
| FLT3 mutation | 
 Gilteritinib alone or combinations with HMA Venetoclax-based combination, (2 drugs or 3 drugs)  | 
||
| NPM1 mutation or MLL rearrangement | 
 Clinical trials with NPM1/MLL inhibitors Venetoclax-based combination, (2 drugs or 3 drugs)  | 
||
| TP53 mutation | Clinical trials | ||
| No mutation | 
 Clinical trials Novel first in class agents HMA-base combinations Immunotherapy: MoAbs ADC BiTE/DART Cellular therapies, CAR T, NK cells…  | 
||