2004Huaxi yaoxue zazhiRequires access

Clinical observation on the effects of low dosage imatinib to chronic myelogenous leukemia in blast crisis

Zhonggan Huang

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Abstract

OBJECTIVE To observe the efficacy and safety of low dosage imatinib in the treatment of chronic myelogenous leukemia in the blast crisis (CML-BC). METHODS 8 patients with CML-BC who had received interferon and hydroxyurea were treated with 200-300 mg·d -1 of oral imatinib for 18 to 94 weeks. RESULS 4 patients achieved complete hematological response and 2 patients achieved major hematological response.Imatinib induced major cytogenetic response in 2 patients and improved cytogenetic response in 2 patients. The adverse effects were little and tolerable. CONCLUSION Low dosage imatinib has also improved hematologic and cytogenetic responses in patients with CML-BC who had failed in previous therapy of interferon and hydroxyurea. Further investigation is required for long_term effects of low dosage imatinib on CML-BC.

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OBJECTIVE To observe the efficacy and safety of low dosage imatinib in the treatment of chronic myelogenous leukemia in the blast crisis (CML-BC). METHODS 8 patients with CML-BC who had received interferon and hydroxyurea were treated with 200-300 mg·d -1 of oral imatinib for 18 to 94 weeks. RESULS 4 patients achieved complete hematological response and 2 patients achieved major hematological response.Imatinib induced major cytogenetic response in 2 patients and improved cytogenetic response in 2 patients. The adverse effects were little and tolerable. CONCLUSION Low dosage imatinib has also improved hematologic and cytogenetic responses in patients with CML-BC who had failed in previous therapy of interferon and hydroxyurea. Further investigation is required for long_term effects of low dosage imatinib on CML-BC.

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Available abstract

OBJECTIVE To observe the efficacy and safety of low dosage imatinib in the treatment of chronic myelogenous leukemia in the blast crisis (CML-BC). METHODS 8 patients with CML-BC who had received interferon and hydroxyurea were treated with 200-300 mg·d -1 of oral imatinib for 18 to 94 weeks. RESULS 4 patients achieved complete hematological response and 2 patients achieved major hematological response.Imatinib induced major cytogenetic response in 2 patients and improved cytogenetic response in 2 patients. The adverse effects were little and tolerable. CONCLUSION Low dosage imatinib has also improved hematologic and cytogenetic responses in patients with CML-BC who had failed in previous therapy of interferon and hydroxyurea. Further investigation is required for long_term effects of low dosage imatinib on CML-BC.

Key concepts: Imatinib, Chronic myelogenous leukemia, Blast Crisis, Adverse effect, Leukemia, Internal medicine, Imatinib mesylate, Pharmacology

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