Abstract
This multicenter randomized phase III study was designed to compare the efficacy and toxicity of IFN alpha-2c (3.5 MU/d) in combination with either araC (10 mg/m(2) d1-10) or hydroxyurea (HU: 25 mg/kg per day) in newly diagnosed CML patients. A total of 114 patients were randomized. Following a median observation period of 36 (range 1-73) months the major cytogenetic response rates were 25 and 27% and the 4-year survival probabilities 62.5 and 63% for the araC and HU group, respectively. While the overall toxicity profile was comparable between both groups, patients in the HU arm exhibited a slightly higher degree of WHO grades 3 and 4 non-hematological toxicities.
Publication types
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Clinical Trial
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Clinical Trial, Phase III
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Multicenter Study
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Randomized Controlled Trial
MeSH terms
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Adult
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Aged
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Antineoplastic Combined Chemotherapy Protocols / adverse effects
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Cytarabine / administration & dosage
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Cytarabine / adverse effects
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Female
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Gastrointestinal Diseases / chemically induced
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Hematologic Diseases / chemically induced
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Humans
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Hydroxyurea / administration & dosage
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Hydroxyurea / adverse effects
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Interferon-alpha / administration & dosage
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Interferon-alpha / adverse effects
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Leukemia, Myeloid, Chronic-Phase / drug therapy*
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Leukemia, Myeloid, Chronic-Phase / mortality
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Life Tables
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Male
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Middle Aged
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Nervous System Diseases / chemically induced
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Recombinant Proteins
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Treatment Outcome
Substances
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Interferon-alpha
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Recombinant Proteins
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Cytarabine
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interferon alfa-2c
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Hydroxyurea