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Table 1 Baseline patient characteristics

From: Multicenter phase II clinical trial of nilotinib for patients with imatinib-resistant or -intolerant chronic myeloid leukemia from the East Japan CML study group evaluation of molecular response and the efficacy and safety of nilotinib

Parameters

Value

Median age, y (range)

62 (19–84)

Men/women

27/22

Chronic phase/accelerated phase

45/4

Median duration of CML, months (range)

46.0 (3.6-208.2)

Median duration of imatinib therapy, months (range)

43.4 (3.1-101.9)

Imatinib-resistant/-intolerant

33/16

Prior TKI therapy

 

Imatinib/dasatinib/bosutinib

49/4/2

Other prior therapy

 

Interferon/hydroxyurea/AraC/BU

9/8/1/1

Cytogenetic response at baseline, Ph +%

 

>95/>65-95/>35-65/>0-36/0

14/6/4/2/23

BCR-ABL1 level at baseline, IS%

 

>10/>1-10/>0.1-1/≤ 0.1

18/7/10/14

Additional chromosomal abnormality, n (%)

5 (15.2)

BCR-ABL1 mutations, n (%)

6 (12.2)

  1. CML, chronic myeloid leukemia; mo, months; TKI, tyrosine kinase inhibitor; AraC, cytarabine; BU, busulfan; Ph +%, % of Philadelphia chromosome-positive patients; IS%, international scale %.