Table 1.

Patient baseline characteristics and prior therapy

VariableNumber (%)
Gender, male 14 (72.7) 
Age in years, median (range) 59 (29-76) 
Disease status 
 Relapsed 10 (52.6) 
 Refractory 8 (42.1) 
 Other* 1 (5.3) 
ELN cytogenetic risk 
 Favorable 1 (5.3) 
 Intermediate 17 (89.5) 
 Adverse 1 (5.3) 
Peripheral WBC ×109 cells/L, median (range) 4.8 (<0.3-79.1) 
Peripheral myeloblast %, median (range) 17.5 (0-98) 
Bone marrow myeloblast %, median (range) 52.5 (2-94) 
FLT3 mutation status 
 ITD positive 17 (89.5) 
 Both ITD and TKD positive 1 (4.5) 
 TKD positive 1 (4.5) 
Bone marrow transplant 
 Pre 11 (57.9) 
 Post 8 (42.1) 
Prior therapy 
 Newly diagnosed 
  7 + 3 1 (5.3) 
  7 + 3 and/or HiDAC + midostaurin 14 (73.7) 
  BI 836858 + azacytidine 1 (5.3) 
  Entospletinib + azacytidine 1 (5.3) 
  Enasidenib 1 (5.3) 
  Unknown 1 (5.3) 
 Relapsed/refractory disease (before gilteritinib) 
  Pacritinib, selinexor + mitoxantrone/etoposide/cytarabine, sorafenib 1 (5.3) 
  Venetoclax + azacytidine, AZD5991 1 (5.3) 
  FLAG + HMA 1 (5.3) 
VariableNumber (%)
Gender, male 14 (72.7) 
Age in years, median (range) 59 (29-76) 
Disease status 
 Relapsed 10 (52.6) 
 Refractory 8 (42.1) 
 Other* 1 (5.3) 
ELN cytogenetic risk 
 Favorable 1 (5.3) 
 Intermediate 17 (89.5) 
 Adverse 1 (5.3) 
Peripheral WBC ×109 cells/L, median (range) 4.8 (<0.3-79.1) 
Peripheral myeloblast %, median (range) 17.5 (0-98) 
Bone marrow myeloblast %, median (range) 52.5 (2-94) 
FLT3 mutation status 
 ITD positive 17 (89.5) 
 Both ITD and TKD positive 1 (4.5) 
 TKD positive 1 (4.5) 
Bone marrow transplant 
 Pre 11 (57.9) 
 Post 8 (42.1) 
Prior therapy 
 Newly diagnosed 
  7 + 3 1 (5.3) 
  7 + 3 and/or HiDAC + midostaurin 14 (73.7) 
  BI 836858 + azacytidine 1 (5.3) 
  Entospletinib + azacytidine 1 (5.3) 
  Enasidenib 1 (5.3) 
  Unknown 1 (5.3) 
 Relapsed/refractory disease (before gilteritinib) 
  Pacritinib, selinexor + mitoxantrone/etoposide/cytarabine, sorafenib 1 (5.3) 
  Venetoclax + azacytidine, AZD5991 1 (5.3) 
  FLAG + HMA 1 (5.3) 

7 + 3, cytarabine continuously for 7 days with an anthracycline days 1 to 3; FLAG, fludarabine with HiDAC, idarubicin, and granulocyte-colony stimulating factor; HiDAC, high-dose cytarabine; HMA, hypomethylating agent.

*

Gilteritinib treatment post-transplant.

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