Abstract |
A phase II study of 3-deazauridine (DAUR) showed poor activity in previously treated patients with advanced colorectal adenocarcinoma. There were no responses among 15 patients treated on a dose schedule of 1200 mg/m2/day for 5 days repeated at 3-week intervals. Toxicity included mild nausea and vomiting, occasional mucositis, diarrhea, and dizziness. A minimal degree of myelosuppression was observed.
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Authors | S Bruno, P J Creaven, E Ledesma, D Poster, J Yoon, A Mittelman |
Journal | American journal of clinical oncology
(Am J Clin Oncol)
Vol. 5
Issue 1
Pg. 69-71
(Feb 1982)
ISSN: 0277-3732 [Print] United States |
PMID | 7081140
(Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
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Chemical References |
- Antineoplastic Agents
- 3-Deazauridine
- Uridine
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Topics |
- 3-Deazauridine
(administration & dosage, adverse effects)
- Adenocarcinoma
(drug therapy)
- Adult
- Aged
- Antineoplastic Agents
(administration & dosage, adverse effects)
- Colonic Neoplasms
(drug therapy)
- Digestive System
(drug effects)
- Drug Evaluation
- Female
- Humans
- Male
- Middle Aged
- Rectal Neoplasms
(drug therapy)
- Uridine
(analogs & derivatives)
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