Literature DB >> 10361112

Sequential homoharringtonine and interferon-alpha in the treatment of early chronic phase chronic myelogenous leukemia.

S O'Brien1, H Kantarjian, C Koller, E Feldman, M Beran, M Andreeff, S Giralt, B Cheson, M Keating, E Freireich, M B Rios, M Talpaz.   

Abstract

Homoharringtonine (HHT) is a novel plant alkaloid that produced a complete hematologic remission (CHR) in 72% of patients with late chronic phase chronic myelogenous leukemia (CML). Cytogenetic (CG) remissions were noted in 31%. In this study, six courses of HHT were administered to 90 patients with early chronic phase CML (< 1 year from diagnosis). Patients then received interferon-alpha (IFN-alpha) with a target dose of 5 MU/m2 daily. Results were compared with those in a prior group of patients treated with IFN-alpha-based therapy between 1982 and 1990. Ninety-two percent of patients achieved CHR with HHT; CG responses were observed in 60% and were major in 27%. Both CHR and CG response rates were significantly higher than those seen in historical control patients after 6 months of IFN-alpha therapy. After receiving HHT, patients required lower doses of IFN-alpha to maintain a CHR. The median dose delivered was 2.4 MU/m2. This reduction in IFN-alpha dose was associated with a lower incidence of myalgia and gastrointestinal (GI) disturbances than that seen in patients treated at the 5 MU/m2 dose. Overall, CG responses were seen in 66% of the patients who received HHT and IFN-alpha compared with 61% of the historical control patients. HHT is a very effective treatment of early chronic phase CML, and ongoing trials are investigating the simultaneous administration of HHT and IFN-alpha, as well as that of HHT and low-dose cytosine arabinoside in patients failing IFN-alpha therapy.

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Year:  1999        PMID: 10361112

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  16 in total

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2.  Omacetaxine: a protein translation inhibitor for treatment of chronic myelogenous leukemia.

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Review 3.  Chronic myeloid leukemia: mechanisms of resistance and treatment.

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Journal:  Hematol Oncol Clin North Am       Date:  2011-10-19       Impact factor: 3.722

Review 4.  Homoharringtonine/omacetaxine mepesuccinate: the long and winding road to food and drug administration approval.

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Journal:  Clin Lymphoma Myeloma Leuk       Date:  2013-06-20

5.  Phase 2 study of subcutaneous omacetaxine mepesuccinate after TKI failure in patients with chronic-phase CML with T315I mutation.

Authors:  Jorge Cortes; Jeff H Lipton; Delphine Rea; Raghunadharao Digumarti; Charles Chuah; Nisha Nanda; Annie-Claude Benichou; Adam R Craig; Mauricette Michallet; Franck E Nicolini; Hagop Kantarjian
Journal:  Blood       Date:  2012-08-15       Impact factor: 22.113

6.  Homoharringtonine as a backbone drug for the treatment of newly diagnosed pediatric acute myeloid leukemia: a report from a single institution in China.

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Review 8.  Chronic myeloid leukemia: pathophysiology, diagnostic parameters, and current treatment concepts.

Authors:  Christian Sillaber; Matthias Mayerhofer; Hermine Agis; Verena Sagaster; Christine Mannhalter; Wolfgang R Sperr; Klaus Geissler; Peter Valent
Journal:  Wien Klin Wochenschr       Date:  2003-08-14       Impact factor: 1.704

Review 9.  Best Practices in Chronic Myeloid Leukemia Monitoring and Management.

Authors:  Simona Soverini; Caterina De Benedittis; Manuela Mancini; Giovanni Martinelli
Journal:  Oncologist       Date:  2016-03-31

10.  Phase 2 study of subcutaneous omacetaxine mepesuccinate for chronic-phase chronic myeloid leukemia patients resistant to or intolerant of tyrosine kinase inhibitors.

Authors:  J Cortes; R Digumarti; P M Parikh; M Wetzler; J H Lipton; A Hochhaus; A R Craig; A-C Benichou; F E Nicolini; H M Kantarjian
Journal:  Am J Hematol       Date:  2013-03-07       Impact factor: 10.047

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