Literature DB >> 2532073

Phase II trial of plicamycin and hydroxyurea in acute myelogenous leukemia.

E Archimbaud1, J Troncy, C Sebban, D Guyotat, Y Devaux, M French, M Moriceau, J J Viala, D Fiere.   

Abstract

A total of 23 patients with high-risk acute myelogenous leukemia (AML) at diagnosis (2 patients), relapsing AML (14) or resistant AML (6) were treated with 25 micrograms/kg i.v. plicamycin every other day for 3 weeks and 500-4,000 mg hydroxyurea per day p. o. according to the WBC count. Aplasia was observed in only two patients. Severe extrahematologic toxicity included sepsis (four cases), vomiting (four patients), toxic hepatitis (three cases), and fibrinopenia (one patient). No partial or complete responses were observed. The 95% confidence interval limit of the overall response rate (CR + PR) was 0-14%.

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Year:  1989        PMID: 2532073     DOI: 10.1007/bf00689589

Source DB:  PubMed          Journal:  Cancer Chemother Pharmacol        ISSN: 0344-5704            Impact factor:   3.333


  11 in total

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8.  Mithramycin inhibition of ribonucleic acid synthesis.

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10.  Preliminary observations on the therapy of the myeloid blast phase of chronic granulocytic leukemia with plicamycin and hydroxyurea.

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