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. 2020 Jun 22;34(8):2125–2137. doi: 10.1038/s41375-020-0915-9

Table 1.

Demographic and baseline characteristics across patients with Ph + CP CML.

Characteristic Line of treatment Total (N = 156)
Second-line (n = 46) Third-line (n = 61) Fourth-line (n = 49)
Male, n (%) 23 (50.0) 37 (60.7) 21 (42.9) 81 (51.9)
Age, median (range), years 54.0 (19.0–88.0) 65.0 (27.0–85.0) 61.0 (21.0–85.0) 61.0 (19.0–88.0)
Age group, n (%)
    <65 years 34 (73.9) 30 (49.2) 32 (65.3) 96 (61.5)
    ≥65 years 12 (26.1) 31 (50.8) 17 (34.7) 60 (38.5)
ECOG PS, n (%)
    0 34 (73.9) 40 (65.6) 32 (65.3) 106 (67.9)
    1 12 (26.1) 20 (32.8) 13 (26.5) 45 (28.8)
    2 0 1 (1.6) 4 (8.2) 5 (3.2)
Median (range) duration since CML diagnosis, years 2.2 (0.2–11.4) 5.0 (0.3–18.6) 7.3 (0.7–27.7) 4.7 (0.2–27.7)
Prior TKI, n (%)a
    Imatinib 35 (76.1) 57 (93.4) 49 (100) 141 (90.4)
    Dasatinib 5 (10.9) 41 (67.2) 49 (100) 95 (60.9)
    Nilotinib 6 (13.0) 24 (39.3) 49 (100) 79 (50.6)
Prior interferon alpha, n (%) 2 (4.3) 3 (4.9) 6 (12.2) 11 (7.1)
Resistant to any prior TKI, n (%) 17 (37.0) 35 (57.4) 31 (63.3) 83 (53.2)
Intolerant to all prior TKIs, n (%) 29 (63.0) 26 (42.6) 18 (36.7) 73 (46.8)

Full analysis set.

CML chronic myeloid leukemia, CP chronic phase, ECOG PS Eastern Cooperative Oncology Group performance status, Ph Philadelphia chromosome, TKI tyrosine kinase inhibitor.

aIn the third-line cohort, 37 (60.7%) of patients received prior imatinib and dasatinib, 20 (32.8%) of patients received prior imatinib and nilotinib and 4 (6.6%) of patients received prior dasatinib and nilotinib.