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ID 30705
JaLCDOI
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Author
Takahashi, Isao
Hara, Masamichi
Uchida, Kozaburo
Takaoka, Kazuko
Watanabe, Seiichiro
Lai, Minyu
Hamasaki, Kazuhide
Kohi, Fumikazu
Kitajima, Koichi
Kimura, Ikuro
Adachi, Tomiro
Yorimitsu, Seiichi
Tokioka, Masaaki
Sanada, Hiroshi
Abstract

Relapses in nine patients with acute myelocytic leukemia were treated with a combination of aclarubicin (ACR) and cytosine arabinoside (ara-C). ACR, 40 mg/m2/day, was administered daily by intravenous injection from day 1 to day 3 and ara-C, 60-80 mg/m2/day, divided into 2 doses, was given every 12 h by intravenous infusion from day 1 to day 7. Depending on the state of the bone marrow, ACR-ara-C regimen was modified in administration period and repeated after the resting periods of at least 7 days. Complete remission was obtained in 7 of 9 patients (77.8%). The time required for achieving the complete remission varied from 20 to 55 days with a median of 39 days. The duration of complete remission was from 8 to 52 weeks with a median of 22 weeks. Side effects on digestive system such as nausea, vomiting and anorexia, were seen in all patients, although they were managed by symptomatic treatment. The results indicate the effectiveness of this ACR-ara-C regimen in the clinical management of acute nonlymphocytic leukemia.

Keywords
aclarubicin
cytosine arabinoside
chemotherapy
acute myelocytic leukemia
Amo Type
Brief Note
Publication Title
Acta Medica Okayama
Published Date
1982-02
Volume
volume36
Issue
issue1
Publisher
Okayama University Medical School
Start Page
77
End Page
80
ISSN
0386-300X
NCID
AA00508441
Content Type
Journal Article
language
English
File Version
publisher
Refereed
True
PubMed ID
Web of Science KeyUT