Table 1 Demographics and baseline characteristics for patients

From: Bemcentinib as monotherapy and in combination with low-dose cytarabine in acute myeloid leukemia patients unfit for intensive chemotherapy: a phase 1b/2a trial

 

Phase 1b

Phase 2a

Property

Number of patients

Percentage, %

Number of patients

Percentage, %

Sex [1]

 Female

14

61

12

33

 Male

22

39

24

67

Age (years)

 Median

74.5 (Range 51-85)

 

76 (Range 66–86)

 

 <75

18

50

12

33

 ≥75

18

50

24

67

ECOG at screening

 Median

1 (Range 0–2)

 

1 (Range 0–2)

 

 0

7

19

13

36

 1

19

53

18

50

 2

10

28

5

14

Type of cancer

 AML

34

94

36

100

 MDS (high risk)

2

6

0

0

% blasts at screening (bone marrow)

 <10

4

11

5

14

 ≥10

26

72

31

86

 missing

6

17

0

0

Cytogenetic Profile [2]

 favorable

2

6

7

19

 intermediate

3

8

13

36

 adverse

7

19

14

39

 missing

24

67

2

6

Disease status

 Treatment-naive

2

6

6

17

 relapsed

16

44

21

58

 refractory

12

33

9

25

 other

6

17

0

0

No. lines prior therapy

 Median

2 (Range 1–6)

 

1 (Range 0–8)

 

 0

1

3

6

17

 1

12

33

15

42

 2

11

31

9

25

 ≥3

12

33

6

17

Prior treatment

 Venetoclax

0

0

11

31

 Allo-HCT

2

6

0

0

 Intensive chemotherapy

18

50

9

25

FLT3 status

 Wildtype

17

47

21

58

 Mutated

7

19

5

14

 of which ITD

2

6

1

3

 Missing

12

33

10

28

  1. Allo-HCT Allogeneic hematopoietic cell transplantation, AML Acute Myeloid leukemia, ECOG Eastern Cooperative Oncology Group performance status, ITD internal tandem duplication, MDS Myelodysplastic syndrome, No. number. Headings and subheadings in bold.
  2. [1] Self-reported.
  3. [2] Cytogenetic risk was assessed by each study site using locally defined criteria. DE cohort patients were assessed as low, medium or high risk. LDAC Cohort patients were assessed as favorable, intermediate or adverse risk. Where specific data was provided, classification was consistent with ELN 2017 criteria.