Rationale: At present, virtually no evidence exists regarding mid to long-term patient-reported health outcomes (e.g., health related quality of life-HRQOL) of CML patients treated with Imatinib. Purpose: the results of this research will provide preliminary evidence-based data on an number of issues from the patients' perspective, including adherence to therapy issues.
OBJECTIVES: Primary: to investigate a number of mid to long-term HRQOL issues in Chronic Myeloid Leukemia (CML) patients with complete cytogenetic response treated with Imatinib as First Line Therapy. Secondary evaluation of: * Psychological wellbeing. * Fatigue. * Adherence to therapy issues. * Symptom burden. * Possible association between social-demographic and clinical variables with patient reported health outcomes. OUTLINE:This is a multicenter study. SAMPLE SIZE: Sample size estimation has not been performed considering the nature of the study and the lack of preliminary data to hypothesize the number of possible eligible patients in each center. DURATION OF THE STUDY: The recruitment period is estimated in approximately 6 to 12 months.
Study Type
OBSERVATIONAL
Enrollment
448
Questionnaires
Ist.Ematologia e Oncologia Medica L.e A. Seragnoli
Bologna, Bologna, Italy
Number of mid to long-term HRQOL issues in Chronic Myeloid Leukemia (CML) patients with complete cytogenetic response treated with Imatinib as First Line Therapy.
Time frame: By the end of the study.
Psychological wellbeing.
Time frame: By the end of the study.
Fatigue.
Time frame: By the end of the study.
Adherence to therapy issues.
Time frame: By the end of the study.
Symptom burden.
Time frame: By the end of the study.
Possible association between socio-demographic and clinical variables with patient reported health outcomes.
Time frame: By the end of the study.
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