Literature DB >> 6871884

Phase I trial of homoharringtonine administered as a 5-day continuous infusion.

C J Coonley, R P Warrell, C W Young.   

Abstract

Homoharringtonine (HHT) has substantial cytotoxic activity against cell lines of experimental tumors. Moreover, the drug has been used extensively in the People's Republic of China for the treatment of patients with acute leukemia. Since rapid injections of HHT can produce serious hypotension and cardiac arrhythmias, we evaluated HHT administered as a continuous infusion for 5 days in patients with advanced cancer. Thirty-one patients were treated with HHT at doses which ranged from 0.2 to 3.75 mg/m2/day. Myelosuppression (both leukopenia and thrombocytopenia) was the dose-limiting toxic reaction. Platelet recovery was delayed in five patients; the median time to platelet nadir was 31 days in patients treated at the highest dose level. Sinus tachycardia occurred frequently, but the relation of this effect to drug administration was uncertain. Serious cardiac arrhythmias and hypotension were not observed using this schedule. We conclude that HHT can be safely administered as a continuous infusion. A daily dose of 3.25 mg/m2 x 5 days is recommended for phase II studies.

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Year:  1983        PMID: 6871884

Source DB:  PubMed          Journal:  Cancer Treat Rep        ISSN: 0361-5960


  11 in total

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2.  High-dose homoharringtonine versus standard-dose daunorubicin is effective and safe as induction and post-induction chemotherapy for elderly patients with acute myeloid leukemia: a multicenter experience from China.

Authors:  Bin-Tao Huang; Qing-Chun Zeng; Jessica Yu; Xiao-Li Liu; Zhen Xiao; Hong-Qian Zhu
Journal:  Med Oncol       Date:  2011-01-22       Impact factor: 3.064

3.  Homoharringtonine: a phase I evaluation.

Authors:  J A Stewart; I H Krakoff
Journal:  Invest New Drugs       Date:  1985       Impact factor: 3.850

4.  Drug monographs: cabozantanib and omacetaxine.

Authors:  Dominic A Solimando; Kristin V Ho; J Aubrey Waddell
Journal:  Hosp Pharm       Date:  2013-05

5.  Effect of homoharringtonine on the viability of murine leukemia P388 cells resistant to either adriamycin, vincristine, or 1-beta-D-arabinofuranosylcytosine.

Authors:  L J Wilkoff; D A Dulmadge; W R Laster; D P Griswold
Journal:  Cancer Chemother Pharmacol       Date:  1989       Impact factor: 3.333

6.  Biologic and pharmacologic effects of harringtonine on human leukemia-lymphoma cells.

Authors:  Y Takemura; T Ohnuma; T C Chou; T Okano; J F Holland
Journal:  Cancer Chemother Pharmacol       Date:  1985       Impact factor: 3.333

7.  Responses of human bone marrow progenitor cells to fluoro-ara-AMP, homoharringtonine, and elliptinium.

Authors:  G E Umbach; V Hug; G Spitzer; H Thames; B Drewinko
Journal:  Invest New Drugs       Date:  1984       Impact factor: 3.850

8.  Evaluation of homoharringtonine efficacy in the treatment of squamous cell carcinoma of the head and neck: a phase II Illinois Cancer Council Study.

Authors:  M A Runge-Morris; M S Kies; E Vokes; R Blough; L Weidner; R Knop; K Rowland
Journal:  Invest New Drugs       Date:  1989-07       Impact factor: 3.850

9.  A phase I dose-finding and pharmacokinetic study of subcutaneous semisynthetic homoharringtonine (ssHHT) in patients with advanced acute myeloid leukaemia.

Authors:  V Lévy; S Zohar; C Bardin; A Vekhoff; D Chaoui; B Rio; O Legrand; S Sentenac; P Rousselot; E Raffoux; F Chast; S Chevret; J P Marie
Journal:  Br J Cancer       Date:  2006-07-18       Impact factor: 7.640

Review 10.  Homoharringtonine and omacetaxine for myeloid hematological malignancies.

Authors:  Shuqing Lü; Jianmin Wang
Journal:  J Hematol Oncol       Date:  2014-01-03       Impact factor: 17.388

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