Flowchart for the Therapy of Newly Diagnosed Acute Myeloid Leukemia (AML) - Flowchart
Flowchart for the Therapy of Newly Diagnosed Acute Myeloid Leukemia (AML) - Flowchart
«Flowchart»

Diagnosis AML

Diagnosis AML

Diagnosis AML

Diagnosis AML

Previously untreateda 

Previously untreateda 

Previously untreateda  a  a Previously untreated[a]

Refractory or relapsed

Refractory or relapsed

Refractory or relapsed Refractory or relapsed

Refractory (No CR) or relapsed

Refractory (No CR) or relapsed

Refractory (No CR) or relapsed Refractory (No CR) or relapsed

If CR, Consolidation therapy: IDACd 

If CR, Consolidation therapy: IDACd 

If CR, Consolidation therapy: IDACd 

If CR, Consolidation therapy: d  d

If CR, Consolidation therapy: Allogeneic HCT (preferred), or IDAC or autologous HCT if age <60d 

If CR, Consolidation therapy: Allogeneic HCT (preferred), or IDAC or autologous HCT if age <60d 

If CR, Consolidation therapy: Allogeneic HCT (preferred), or IDAC or autologous HCT if age <60d 

If CR, Consolidation therapy: d  d

If CR, Investigational therapyd 

If CR, Investigational therapyd 

If CR, Investigational therapyd 

If CR, d  d

If CR, Consolidation therapy: Allogeneic HCT (alternative donor transplant if no HLA-matched donor available)d 

If CR, Consolidation therapy: Allogeneic HCT (alternative donor transplant if no HLA-matched donor available)d 

If CR, Consolidation therapy: Allogeneic HCT (alternative donor transplant if no HLA-matched donor available)d 

If CR, Consolidation therapy: d  d

If CR, Investigational therapyd 

If CR, Investigational therapyd 

If CR, Investigational therapyd 

If CR, d  d

End

End

End

End

End

End

HCT, hematopoietic cell transplantation; HLA, human leukocyte antigen; IDAC, intermediate dose cytarabine.

HCT, hematopoietic cell transplantation; HLA, human leukocyte antigen; IDAC, intermediate dose cytarabine.

HCT, hematopoietic cell transplantation; HLA, human leukocyte antigen; IDAC, intermediate dose cytarabine.

a  Risk stratification according to the European LeukemiaNet.

a  Risk stratification according to the European LeukemiaNet.

a  Risk stratification according to the European LeukemiaNet.

a

b  Younger pts (<60-65 years) should routinely be offered investigational therapy on a backbone of standard chemotherapy for induction and consolidation.

b  Younger pts (<60-65 years) should routinely be offered investigational therapy on a backbone of standard chemotherapy for induction and consolidation.

b  Younger pts (<60-65 years) should routinely be offered investigational therapy on a backbone of standard chemotherapy for induction and consolidation.

b

c  Older pts, especially those >65 years or with adverse-risk disease, or those who are unfit for intensive daunorubicin + cytarabine regimens, may be considered for investigational therapy alone or in combination with lower intensity chemotherapy regimens (azacitidine, decitabine).

c  Older pts, especially those >65 years or with adverse-risk disease, or those who are unfit for intensive daunorubicin + cytarabine regimens, may be considered for investigational therapy alone or in combination with lower intensity chemotherapy regimens (azacitidine, decitabine).

c  Older pts, especially those >65 years or with adverse-risk disease, or those who are unfit for intensive daunorubicin + cytarabine regimens, may be considered for investigational therapy alone or in combination with lower intensity chemotherapy regimens (azacitidine, decitabine).

c

d  Investigational therapy as maintenance should be considered if available (after consolidation for younger pts and older pts with favorable-risk disease, and for all other older pts after induction).

d  Investigational therapy as maintenance should be considered if available (after consolidation for younger pts and older pts with favorable-risk disease, and for all other older pts after induction).

d  Investigational therapy as maintenance should be considered if available (after consolidation for younger pts and older pts with favorable-risk disease, and for all other older pts after induction).

d

Salvage treatment

Salvage treatment

Salvage treatment

Pt with primary induction failure and candidate for myeloablative allogeneic HCT or CR2 achieved with salvage treatment, and has suitable donor available

Pt with primary induction failure and candidate for myeloablative allogeneic HCT or CR2 achieved with salvage treatment, and has suitable donor available

Pt with primary induction failure

Pt with primary induction failure and candidate for myeloablative allogeneic HCT or CR2 achieved with salvage treatment, and has suitable donor available

Pt with primary induction failure and candidate for myeloablative allogeneic HCT or CR2 achieved with salvage treatment, and has suitable donor available

Pt with primary induction failure and candidate for myeloablative allogeneic HCT or CR2 achieved with salvage treatment, and has suitable donor available

Yes: Allogeneic HCT

Yes: Allogeneic HCT

Yes: Yes

No: Investigational therapy, autologous HCT considered for favorable-risk pts in CR2 with prolonged CR1 duration (>12 months)

No: Investigational therapy, autologous HCT considered for favorable-risk pts in CR2 with prolonged CR1 duration (>12 months)

No: No

Favorable-risk

Favorable-risk

Favorable-risk

Intermediate-risk

Intermediate-risk

Intermediate-risk

Adverse-risk

Adverse-risk

Adverse-risk

Either option acceptable

Either option acceptable

Either option acceptable

Induction therapy: Daunorubicin + Cytarabine-based regimen

Induction therapy: Daunorubicin + Cytarabine-based regimen

Induction therapy: Induction therapy

Investigational therapyb 

Investigational therapyb 

b  b Investigational therapy[b]

Refractory (No CR) or relapsed

Refractory (No CR) or relapsed

Refractory (No CR) or relapsed

Refractory (No CR) or relapsed

If CR, Investigational therapyd 

If CR, Investigational therapyd 

If CR, Investigational therapyd 

If CR, d  d

Either option acceptable

Either option acceptable

Either option acceptable

Induction therapy: Daunorubicin + Cytarabine-based regimenb  ,c 

Induction therapy: Daunorubicin + Cytarabine-based regimenb  ,c 

Induction therapy: b  b ,c c Induction therapy

Investigational therapyc 

Investigational therapyc 

c  c Investigational therapy[c]

Either option acceptable

Either option acceptable

Either option acceptable

Induction therapy: Daunorubicin + Cytarabine-based regimenb  ,c 

Induction therapy: Daunorubicin + Cytarabine-based regimenb  ,c 

Induction therapy: b  b ,c c Induction therapy

Investigational therapyc 

Investigational therapyc 

c  c Investigational therapy[c]