Table 2

Patient disposition by PK category on day 29 steady-state imatinib trough level

Quartile 1, n=87, no, (%)Quartiles 2 and 3, n=178, no. (%)Quartile 4, n=86, no. (%)
Still on imatinib up to 5 y 51 (58.6) 129 (72.5) 66 (76.7) 
Discontinued imatinib 36 (41.4) 49 (27.5) 20 (23.3) 
    Unsatisfactory effect* 16 (18.4) 27 (15.2) 7 (8.1) 
    Adverse event(s) 4 (4.6) 5 (2.8) 6 (7.0) 
    Death 1 (1.1) 4 (2.2) 1 (1.2) 
    Transplantation 5 (5.7) 5 (2.8) 
    Other reasons 10 (11.5) 8 (4.5) 6 (7.0) 
Quartile 1, n=87, no, (%)Quartiles 2 and 3, n=178, no. (%)Quartile 4, n=86, no. (%)
Still on imatinib up to 5 y 51 (58.6) 129 (72.5) 66 (76.7) 
Discontinued imatinib 36 (41.4) 49 (27.5) 20 (23.3) 
    Unsatisfactory effect* 16 (18.4) 27 (15.2) 7 (8.1) 
    Adverse event(s) 4 (4.6) 5 (2.8) 6 (7.0) 
    Death 1 (1.1) 4 (2.2) 1 (1.2) 
    Transplantation 5 (5.7) 5 (2.8) 
    Other reasons 10 (11.5) 8 (4.5) 6 (7.0) 
*

Including 8 patients who crossed over to interferon and cytarabine (IFN+Ara-C) due to lack of response or loss of response (3, 5, and 0 patients, respectively).

Including 2 patients who crossed over to IFN+Ara-C due to intolerance of imatinib.

Other reasons include the following: subject withdrew consent, protocol violation, loss to follow up, abnormal test procedure, and administrative problems.

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