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dc.contributor.authorWilkinson, Peter M
dc.contributor.authorO'Neill, Paul A
dc.contributor.authorThatcher, Nick
dc.contributor.authorLucas, S B
dc.date.accessioned2010-07-21T11:45:08Z
dc.date.available2010-07-21T11:45:08Z
dc.date.issued1983
dc.identifier.citationPharmacokinetics of high-dose cyclophosphamide in patients with metastatic bronchogenic carcinoma. 1983, 11 (3):196-9 Cancer Chemother. Pharmacol.en
dc.identifier.issn0344-5704
dc.identifier.pmid6640827
dc.identifier.doi10.1007/BF00254204
dc.identifier.urihttp://hdl.handle.net/10541/108054
dc.description.abstractCyclophosphamide (CP) was administered to eight patients with metastatic bronchial carcinoma in escalating doses of 1.5, 2.5, and 3.5 g/m2 at intervals of 3 weeks. The proportion of the administered dose converted into alkylating metabolites was similar for each dose and there was no evidence to suggest that the enzyme system responsible for activating CP was saturated even with the highest dose. Considerable between-patient variation in drug metabolism was observed, but within each patient the fraction metabolised remained constant.
dc.language.isoenen
dc.subjectLung Canceren
dc.subject.meshAdult
dc.subject.meshAlkylation
dc.subject.meshCarcinoma, Bronchogenic
dc.subject.meshCyclophosphamide
dc.subject.meshDose-Response Relationship, Drug
dc.subject.meshFemale
dc.subject.meshHumans
dc.subject.meshKinetics
dc.subject.meshLeukocyte Count
dc.subject.meshLung Neoplasms
dc.subject.meshMale
dc.subject.meshMiddle Aged
dc.subject.meshNeutrophils
dc.titlePharmacokinetics of high-dose cyclophosphamide in patients with metastatic bronchogenic carcinoma.en
dc.typeArticleen
dc.contributor.departmentDepartment of Clinical Pharmacology, Christie Hospital and Holt Radium Institute, M20 9BX Manchester, England.en
dc.identifier.journalCancer Chemotherapy and Pharmacologyen
html.description.abstractCyclophosphamide (CP) was administered to eight patients with metastatic bronchial carcinoma in escalating doses of 1.5, 2.5, and 3.5 g/m2 at intervals of 3 weeks. The proportion of the administered dose converted into alkylating metabolites was similar for each dose and there was no evidence to suggest that the enzyme system responsible for activating CP was saturated even with the highest dose. Considerable between-patient variation in drug metabolism was observed, but within each patient the fraction metabolised remained constant.


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