The main aim of this study is to observe correction of the hemoglobin level in the patients under chemotherapy, treated with epoetin alfa biosimilar and presenting with a solid tumor or a lymphoma or a myeloma.
This is a non-interventional, descriptive, national, multi-site, longitudinal and prospective observational study with adults patients who are suffering from cancer or malignant blood disease and whose chemotherapy treatment has induced symptomatic anemia and being treated with biosimilar of epoetin to correct haemoglobin levels.
Study Type
OBSERVATIONAL
Enrollment
2,333
Change and corrected Hemoglobin levels
Participants who have hemoglobin values between 11 and 12 g/dl after 6 months of treatment.
Time frame: 6 months
Observe evolution of the biological indicators
Observe evolution of the biological indicators: hemoglobin, hematocrit, reticulocytes, serum iron, ferritin, transferrin saturation
Time frame: 6 months
Study the profiles of treated patients
Time frame: 6 months
Assess the reasons for the prescriber's treatment regimens
Time frame: 6 months
Assess the correlations between the prescribing oncologists' treatment regimens and the patient characteristics
Time frame: 6 months
Observation of the safety profiles of the Product (Epoetin Alfa)
Time frame: 6 months
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Agen, France
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Aix-en-Provence, France
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Aix-en-Provence, France
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Aix-en-Provence, France
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Ajaccio, France
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Albi, France
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Amboise, France
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Amilly, France
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Annecy, France
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Antibes, France
...and 162 more locations