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Publication Type
Journal Article
Author, Analytic
White, Jeffrey D.; Wharfe, Gillian H.; Stewart, D. M.; Maher, V. E.; Eicher, D.; Herring, B.; Derby, M.; Jackson-Booth, P. G.; Marshall, M.; Lucy, D.; Jain, A.; Cranston, Beverley; Hanchard, Barrie; Lee, C. C. ; Top, L. E.; Fleisher, Thomas A.; Nelson, David L.; Waldmann, Thomas A.
Author Affiliation, Ana.
Department of Pathology
Article Title
The combination of zidovudine and interferon alpha-2B in the treatment of adult T-cell leukemia/lymphoma
Medium Designator
n/a
Connective Phrase
n/a
Journal Title
Leukemia and Lymphoma
Translated Title
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Reprint Status
n/a
Date of Publication
2001
Volume ID
40
Issue ID
3-4
Page(s)
287-94
Language
eng
Connective Phrase
n/a
Location/URL
n/a
ISSN
1042-8194
Notes
n/a
Abstract
Adult T-cell leukemia/lymphoma (ATL) is frequently a very aggressive malignancy with a poor survival despite aggressive multiagent chemotherapy. The combination of the antiretroviral drug zidovudine (AZT) and interferon alpha (IFNalpha) has been reported to induce remissions in patients with ATL. The purpose of this study was to evaluate the clinical response and toxicity following administration of a combination of IFNalpha-2b and AZT in patients with human T-cell lymphotropic virus type I (HTLV-I)-associated ATL. Eighteen patients with ATL (chronic. crisis, acute or lymphoma type) were treated with the combination of AZT (50 - 200 mg orally 5 times a day) and IFNalpha- 2b (2.5 - 10 million units subcutaneously daily). Three patients had objective responses lasting more than one month. One patient had a clinical complete remission, lasting 21.6 months and two patients had partial remissions lasting 3.7 and 26.5 months. Six patients were not considered evaluable for response due to short and/or interrupted periods of treatment. Seventeen patients have died with a median survival time after initiation of therapy of 6 months. Neutropenia and thrombocytopenia were the dose limiting toxicities. In conclusion, the response rate in this study was lower than noted in the two previous published series. This may be due to the amount and type of prior treatment our patients had received.....
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