Chronic Myeloid Leukemia
Conditions
Brief summary
The purpose of this study is to evaluate treatment patterns and associated outcomes for CP-CML patients who fail Imatinib 400 mg daily in a real-world setting.
Detailed description
Time Perspective: Retrospective and Prospective
Interventions
None listed
Sponsors
Study design
Eligibility
Inclusion criteria
For more information regarding BMS clinical trial participation, please visit www.BMSStudyConnect.com. Inclusion Criteria: * Adult patients (18 years or older) in Chronic phase CML patients who have been treated with Imatinib 400 mg and have failed.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Complete Cytogenic Response (CCyR) for CP-CML patients who failed Imatinib 400 mg daily | At 3 months post treatment change |
Secondary
| Measure | Time frame |
|---|---|
| Prognostic factors (clinical and demographic characteristics) that influence treatment selection for CP-CML patients who fail imatinib 400 mg daily | Baseline |
| Best response rates achieved by patients if no CCyR | Baseline |