Skip to main content

Table 1 Patient characteristics

From: Olverembatinib (HQP1351), a well-tolerated and effective tyrosine kinase inhibitor for patients with T315I-mutated chronic myeloid leukemia: results of an open-label, multicenter phase 1/2 trial

 

Total

Chronic phase CML

Accelerated phase CML

Patient number

165

127

38

Age (y), median (range)

42 (20–74)

43 (20–70)

38.5 (21–74)

Male, n (%)

110 (66.7)

79 (62.2)

31 (81.6)

ECOG performance status, n (%)

0

99 (60.0)

82 (64.6)

17 (44.7)

1

64 (38.8)

43 (33.9)

21 (55.3)

Not done

2 (1.2)

2 (1.6)

0

Time from diagnosis to olverembatinib treatment (y), median (range)

5.7 (0.3–23.2)

5.3 (0.6–23.2)

6.9 (0.3–14.7)

Prior TKIs, n (%)

Imatinib

22 (13.3)

16 (12.6)

6 (15.8)

Imatinib/dasatinib

60 (36.4)

47 (37.0)

13 (34.2)

Imatinib/nilotinib

26 (15.8)

22 (17.3)

4 (10.5)

Imatinib/dasatinib/nilotinib

45 (27.3)

35 (27.6)

10 (26.3)

Nilotinib

6 (3.6)

4 (3.1)

2 (5.3)

Dasatinib

2 (1.2)

1 (0.8)

1 (2.6)

Dasatinib/nilotinib

4 (2.4)

2 (1.6)

2 (5.3)

Number of lines of prior TKI therapy, n (%)

1

30 (18.2)

21 (16.5)

9 (23.7)

2

90 (54.5)

71 (55.9)

19 (50.0)

 ≥ 3

45 (27.3)

35 (27.6)

10 (26.3)

BCR-ABL1 mutation status by Sanger sequencing, n (%)

No mutation

24 (14.5)

23 (18.1)

1 (2.6)

T315I single mutation

102 (61.8)

77 (60.6)

25 (65.8)

T315I + additional mutations

25 (15.2)

16 (12.6)

9 (23.7)

Other mutations

14 (8.5)

11 (8.7)

3 (7.9)

BCR-ABL1 mutation status by next-generation sequencing, n (%)

No mutation

20 (16.9)

19 (20.2)

1 (4.2)

T315I single mutation

53 (44.9)

41 (43.6)

12 (50.0)

T315I + additional mutations

19 (16.1)

15 (16.0)

4 (16.7)

Other mutations

14 (11.9)

12 (12.8)

2 (8.3)

Compound mutations

12 (10.2)

7 (7.4)

5 (20.8)

ACA, n (%)

   

Yes

28 (17.0)

10 (7.9)

18 (47.4)

No

137 (83.0)

117 (92.1)

20 (52.6)

  1. ACA additional chromosomal abnormalities, CML chronic myeloid leukemia, ECOG Eastern Cooperative Oncology Group, TKI tyrosine kinase inhibitor