Table 2

Discontinuation from treatment

Reason, n (%)IM + DAS resistant (n = 37)IM + DAS intolerant (n = 50)IM + NI resistant (n = 27)IM + DAS ± NI (n = 4)*Total (n = 118)
Discontinued treatment 31 (84) 34 (68) 16 (59) 3 (75) 84 (71) 
    Unsatisfactory response (efficacy) 12 (32) 7 (14) 5 (19) 1 (25) 25 (21) 
    AE 6 (16) 15 (30) 3 (11) 24 (20) 
    Disease progression 8 (22) 4 (8) 6 (22) 2 (50) 20 (17) 
    Death 2 (5) 2 (4) 4 (3) 
    Patient request 2 (4) 1 (4) 3 (3) 
    Lost to follow-up 2 (5) 2 (2) 
    Investigator request 1 (4) 1 (1) 
    Protocol violation 1 (2) 1 (1) 
    Other 1 (3) 3 (6) 4 (3) 
Reason, n (%)IM + DAS resistant (n = 37)IM + DAS intolerant (n = 50)IM + NI resistant (n = 27)IM + DAS ± NI (n = 4)*Total (n = 118)
Discontinued treatment 31 (84) 34 (68) 16 (59) 3 (75) 84 (71) 
    Unsatisfactory response (efficacy) 12 (32) 7 (14) 5 (19) 1 (25) 25 (21) 
    AE 6 (16) 15 (30) 3 (11) 24 (20) 
    Disease progression 8 (22) 4 (8) 6 (22) 2 (50) 20 (17) 
    Death 2 (5) 2 (4) 4 (3) 
    Patient request 2 (4) 1 (4) 3 (3) 
    Lost to follow-up 2 (5) 2 (2) 
    Investigator request 1 (4) 1 (1) 
    Protocol violation 1 (2) 1 (1) 
    Other 1 (3) 3 (6) 4 (3) 

IM indicates imatinib; DAS, dasatinib; and NI, nilotinib.

*

Includes 3 patients who previously received all 3 inhibitors and 1 patient with NI intolerance.

Includes patient noncompliance (n = 2), lack of finances (n = 1), and started chemotherapy for gastric adenocarcinoma (n = 1).

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