Phase 2 study of the treatment discontinuation after the change from imatinib to Interferon-alpha in chronoic myeloid leukemia patients who maintained major molecular remission.
- Conditions
- Chronic myeloid leukemia in 1st chronic phase and major molecular response sustained for more than 2 years with imatinib
- Registration Number
- JPRN-UMIN000002838
- Lead Sponsor
- Kanto CML collaborative study group
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 15
Not provided
1) Patients with another primary malignancy except if the other primary malignancy is neither currently clinically significant or requiring active intervention. 2) Patients with uncontrolled active infection. 3) Patients with suspicion of interstitial pneumonitis. 4) History of depression. 5) Patients with uncontrolled diabetes. 6) Patients who currently receiving systemic treatment with corticoid or immunosuppressive drugs. 7) Patients whose physicians consider not appropriate.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Among evaluable patients, the ratio of patients who maintained MMR 12 months after stop of IFN.
- Secondary Outcome Measures
Name Time Method