Publication: Efficacy and Toxicity of Idarubicin Versus High-dose Daunorubicin for Induction Chemotherapy in Adult Acute Myeloid Leukemia: A Systematic Review and Meta-analysis
Issued Date
2018-12-01
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ISSN
21522669
21522650
21522650
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2-s2.0-85053732903
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Mahidol University
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SCOPUS
Bibliographic Citation
Clinical Lymphoma, Myeloma and Leukemia. Vol.18, No.12 (2018), 814-821.e3
Suggested Citation
Weerapat Owattanapanich, Natthida Owattanapanich, Smith Kungwankiattichai, Patompong Ungprasert, Theera Ruchutrakool Efficacy and Toxicity of Idarubicin Versus High-dose Daunorubicin for Induction Chemotherapy in Adult Acute Myeloid Leukemia: A Systematic Review and Meta-analysis. Clinical Lymphoma, Myeloma and Leukemia. Vol.18, No.12 (2018), 814-821.e3. doi:10.1016/j.clml.2018.08.008 Retrieved from: https://repository.li.mahidol.ac.th/handle/20.500.14594/44967
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Title
Efficacy and Toxicity of Idarubicin Versus High-dose Daunorubicin for Induction Chemotherapy in Adult Acute Myeloid Leukemia: A Systematic Review and Meta-analysis
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Abstract
© 2018 The Authors The present meta-analysis compared the efficacy and toxicity between idarubicin (IDA) and high-dose daunorubicin (HDD) for induction therapy for adult acute myeloid leukemia (AML). Across the 5 included studies, patients who had received IDA had a significantly greater complete remission rate after first induction therapy and lower rate of refractory AML after induction therapy compared with those who received had HDD. Background: The 2 main formulations of anthracycline used for acute myeloid leukemia (AML) induction therapy are idarubicin (IDA) and daunorubicin. Patients and Methods: The present systematic review and meta-analysis compared the efficacy and toxicity between IDA and high-dose daunorubicin (HDD) for induction therapy for adult AML. Relevant studies reported before June 2018 were searched from the Medline and Embase databases. Results: A total of 5 studies with 1809 participants (3 randomized controlled studies and 2 retrospective cohort studies) met the eligibility criteria and were included in the meta-analysis. The patients in the IDA arm for induction therapy had a significantly greater complete response rate after the first course of induction therapy compared with those in the HDD arm (66.7% vs. 61.1%, respectively; odds ratio, 1.23; P =.04; I 2 = 0%). A significantly lower rate of refractory AML was also observed in the IDA group than in the HDD group (16.8% vs. 20.7%, respectively; odds ratio, 0.77; P =.04; I 2 = 0%). However, no difference was found in the long-term overall survival between the 2 groups. Also, the induction mortality rate, febrile neutropenia rate, and cardiotoxicity rate were not significantly different between the 2 groups. The major limitation was the relatively small number of included studies, which could have limited the power of the meta-analysis to demonstrate significant long-term benefits. Conclusion: The complete response rate after the first course of induction therapy was significantly greater among adult patients with AML who had received IDA as part of induction therapy compared with those who had received HDD.