This is a prospective, non-interventional study conducted in CP-CML patients receiving dasatinib who are enrolled by a sample of hematologists in France.
Study Type
OBSERVATIONAL
Enrollment
177
Non-Interventional
Local Institution
Paris, France
Incidence of CP-CML patients remaining on dasatinib treatment
Time frame: 24 months
Distribution of median age of CP-CML patients receiving dasatinib
Time frame: 24 months
Distribution of sex ratio of CP-CML patients receiving dasatinib
Time frame: 24 months
Distribution of concomitant treatment of CP-CML patients receiving dasatinib
Time frame: 24 months
Distribution of cardiovascular risk factors of CP-CML patients receiving dasatinib
Time frame: 24 months
Distribution of body mass index (BMI) of CP-CML patients receiving dasatinib
Time frame: 24 months
Distribution of comorbidities of CP-CML patients receiving dasatinib
Time frame: 24 months
Distribution of disease characteristics duration between diagnosis and drug initiation in CP-CML patients receiving dasatinib
Time frame: 24 months
Distribution disease characteristics of last known molecular response in CP-CML patients receiving dasatinib
Time frame: 24 months
SOKAL distribution of disease characteristics of CP-CML patients receiving dasatinib
Time frame: 24 months
Distribution of prior treatment(s) of CP-CML patients receiving dasatinib
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Time frame: 24 months
Incidence of initiating dasatinib due to suboptimal response
Time frame: 24 months
Incidence of initiating dasatinib due to failure
Time frame: 24 months
Incidence of initiating dasatinib due to intolerance
Time frame: 24 months
Incidence of initiating dasatinib due to convenience
Time frame: 24 months
Incidence of initiating dasatinib due to physician decision
Time frame: 24 months
Incidence of AE's
Time frame: 24 months
Incidence of SAE's
Time frame: 24 months
Utilization of dasatinib
Time frame: 24 months
Incidence of complete molecular response (CMR)
Time frame: Up to 24 months
Incidence of major molecular response (MMR)
Time frame: Up to 24 months