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dc.contributor.authorHancock, B
dc.contributor.authorTodd, Ian D
dc.contributor.authorWilkinson, Peter M
dc.date.accessioned2011-06-14T17:39:47Z
dc.date.available2011-06-14T17:39:47Z
dc.date.issued1980-07
dc.identifier.citationChemotherapy of metastatic carcinoma of the breast. 1980, 31 (4):433-6 Clin Radiolen
dc.identifier.issn0009-9260
dc.identifier.pmid7418343
dc.identifier.doi10.1016/S0009-9260(80)80184-X
dc.identifier.urihttp://hdl.handle.net/10541/133130
dc.description.abstractThirty-four patients with metastatic breast carcinoma were treated with the following combination: methotrexate 60 mg/m2 i.v. days 1 and 8,5-fluorouracil 500 mg/m2 i.v. days 1 and 8, cyclophosphamide 100 mg/m2 daily for 14 days, and prednisolone 25 mg b.d. by mouth daily for 14 days. In 21/34 (62%) patients regression of tumour was maintained for at least three months and in six (18%) this was complete. The median duration of response was 15 months (range 6--33) and there was a significant difference in survival between responders and non-responders (P<0.01). Toxicity was acceptable although dose reduction was necessary in eight patients and in three patients treatment had to be discontinued.
dc.language.isoenen
dc.subjectBreast Canceren
dc.subject.meshAdult
dc.subject.meshAntineoplastic Agents
dc.subject.meshBreast Neoplasms
dc.subject.meshCyclophosphamide
dc.subject.meshDrug Therapy, Combination
dc.subject.meshFemale
dc.subject.meshFluorouracil
dc.subject.meshHumans
dc.subject.meshMethotrexate
dc.subject.meshMiddle Aged
dc.subject.meshPrednisolone
dc.subject.meshProspective Studies
dc.titleChemotherapy of metastatic carcinoma of the breast.en
dc.typeArticleen
dc.contributor.departmentDepartments of Radiotherapy and Clinical Pharmacology, Christie Hospital and Holt Radium Institute, Withington, Manchester, UKen
dc.identifier.journalClinical Radiologyen
html.description.abstractThirty-four patients with metastatic breast carcinoma were treated with the following combination: methotrexate 60 mg/m2 i.v. days 1 and 8,5-fluorouracil 500 mg/m2 i.v. days 1 and 8, cyclophosphamide 100 mg/m2 daily for 14 days, and prednisolone 25 mg b.d. by mouth daily for 14 days. In 21/34 (62%) patients regression of tumour was maintained for at least three months and in six (18%) this was complete. The median duration of response was 15 months (range 6--33) and there was a significant difference in survival between responders and non-responders (P<0.01). Toxicity was acceptable although dose reduction was necessary in eight patients and in three patients treatment had to be discontinued.


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