Skip to main content
. Author manuscript; available in PMC: 2015 May 27.
Published in final edited form as: Cancer. 2009 Feb 1;115(3):551–560. doi: 10.1002/cncr.24066

Table 5.

Reasons for Imatinib Discontinuation Documented for Patients Who Had Dose Escalations in the International Randomized Study of Interferon and STI571 Study (N = 106)

Variable No. (%)
Remained on imatinib at data cutoff 42 (40)
    Patients receiving ≥600 mg/d dose at cutoff 31 (29)
Discontinued imatinib* 64 (60)
    Unsatisfactory effect 36 (34)
    Protocol violation 4 (4)
    Adverse event(s) 2 (2)
    Abnormal procedure 2 (2)
    Withdrawal of consent 5 (5)
    Administrative problems/lost to follow-up 2 (2)
    BMT (no longer required study drug) 6 (6)
    Crossed over to IFN-α plus cytarabine 7 (7)

BMT indicates bone marrow transplantation; IFN-α, interferon alpha.

*

Discontinued on or before January 31, 2007.

Patients who discontinued because of unsatisfactory therapeutic effect were on imatinib study treatment for a median of 47 months (range, 8.3– 72.9 months).