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. 2024 May 16;38(7):1522–1533. doi: 10.1038/s41375-024-02278-8

Table 2.

Patient demographics and baseline clinical characteristics.

Demographic variable All patients
N = 48
Evaluable patients
N = 45
Age, median (range), years 56.5 (26–86) 54.0 (26–86)
Age category, n (%)
  18 to <65 years 32 (66.7) 31 (68.9)
  ≥65 years 16 (33.3) 14 (31.1)
  ≥75 years 4 (8.3) 4 (8.9)
Sex, n (%)
  Male 37 (77.1) 36 (80.0)
  Female 11 (22.9) 9 (20.0)
Race, n (%)
  White 23 (47.9) 21 (46.7)
  Asian 12 (25.0) 12 (26.7)
  Unknown 6 (12.5) 5 (11.1)
  Other 6 (12.5) 6 (13.3)
  Black or African American 1 (2.1) 1 (2.2)
Ethnicity, n (%)
  East Asian 10 (20.8) 10 (22.2)
  Other 16 (33.3) 14 (31.1)
  Not reported 14 (29.2) 13 (28.9)
  Unknown 3 (6.3) 3 (6.7)
  Southeast Asian 2 (4.2) 2 (4.4)
  Hispanic or Latino 3 (6.3) 3 (6.7)
ECOG performance status, n (%)
  0 36 (75.0) 33 (73.3)
  1 12 (25.0) 12 (26.7)
No. of prior TKIs
  1a 8 (16.7) 8 (17.8)
  2 15 (31.3) 14 (31.1)
  3 17 (35.4) 16 (35.6)
  ≥4 8 (16.7) 7 (15.6)
Individual prior TKIs
  Bosutinib 3 (6.3) 2 (4.4)
  Dasatinib 33 (68.8) 33 (73.3)
  Imatinib 27 (56.3) 25 (55.6)
  Nilotinib 26 (54.2) 23 (51.1)
  Ponatinib 29 (60.4) 26 (57.8)
  Radotinib 4 (8.3) 4 (8.9)
Reason for discontinuation of last dose of ponatinib
  Intolerance 9 (31.0) 7 (26.9)
  Resistance 14 (48.3) 13 (50.0)
  Other 6 (20.7) 6 (23.1)
Mutations at screening, n (%)
  T315I alone 46 (95.8) 43 (95.6)
  T315I and E255K 1 (2.1) 1 (2.2)
  T315I and E355G 1 (2.1) 1 (2.2)
BCR::ABL1IS at screening, n (%)
  >0.01% to 0.1% 0 0
  >0.1% to 1% 8 (16.7) 8 (17.8)
  >1% to 10% 11 (22.9) 11 (24.4)
  >10% 26 (54.2) 26 (57.8)
  Atypical /e1a2/unknown transcriptsb 3 (6.3) 0

ECOG Eastern Cooperative Oncology Group, TKI tyrosine kinase inhibitor.

aPrior TKIs included dasatinib (n = 5), nilotinib (n = 2), and radotinib (n = 1).

be19a2 transcript, e13a3 (b2a3) transcript, no transcript detected (n = 1, each).