Abstract |
This report describes some experimental and clinical studies showing the following: (1) in animals under protection of mesna the dose of ifosfamide (Ifo) can be increased significantly; (2) fractionated administration of Ifo, cyclophosphamide (CPA), or the stabilized metabolite of cyclophosphamide ( ASTA Z 7557) is less toxic than single push-injection of the same total daily dose and therapeutically more effective; and (3) in humans under the protection of mesna the continuous infusions of ifosfamide over 5 days leads to an increase of the MTD compared with single daily short-term infusion and responses in some solid tumors, e.g., soft tissue sarcomas.
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Authors | H O Klein, P D Wickramanayake, E Christian, C Coerper |
Journal | Cancer
(Cancer)
Vol. 54
Issue 6 Suppl
Pg. 1193-203
(Sep 15 1984)
ISSN: 0008-543X [Print] United States |
PMID | 6432305
(Publication Type: Clinical Trial, Comparative Study, Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Asta Z 7557
- Cyclophosphamide
- Mesna
- Ifosfamide
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Topics |
- Animals
- Clinical Trials as Topic
- Cyclophosphamide
(administration & dosage, analogs & derivatives, toxicity)
- Humans
- Ifosfamide
(administration & dosage, toxicity)
- Infusions, Parenteral
- Kidney
(drug effects)
- Lethal Dose 50
- Male
- Mesna
(administration & dosage)
- Mice
- Mice, Inbred Strains
- Middle Aged
- Neoplasms
(drug therapy)
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