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dc.contributor.authorDawson, N. A.
dc.contributor.authorCostanza, Mary E.
dc.contributor.authorKorzun, A. H.
dc.contributor.authorClamon, G. H.
dc.contributor.authorPollak, M.
dc.contributor.authorVogelzang, N. J.
dc.contributor.authorCarey, R. W.
dc.contributor.authorNorton, L.
dc.date2022-08-11T08:11:05.000
dc.date.accessioned2022-08-23T17:33:02Z
dc.date.available2022-08-23T17:33:02Z
dc.date.issued1991-01-01
dc.date.submitted2007-07-30
dc.identifier.citation<p>Med Pediatr Oncol. 1991;19(4):283-8.</p>
dc.identifier.issn0098-1532 (Print)
dc.identifier.doi10.1002/mpo.2950190413
dc.identifier.pmid1829134
dc.identifier.urihttp://hdl.handle.net/20.500.14038/51084
dc.description.abstractTwenty-two patients with previously untreated metastatic breast cancer and nineteen patients with refractory metastatic breast cancer were treated with trimetrexate (TMTX). Patients received TMTX 8 mg/m2/day if previously treated or 12 mg/m2/day if previously untreated, both given by intravenous bolus days 1-5, every 21 days. None of the patients previously treated for metastatic disease responded to TMTX. There was one partial responder among the 22 patients with previously untreated metastatic disease. The primary toxicity was hematologic and occurred more frequently in patients with a pleural effusion, low serum protein or albumin, or poor performance status. There were three toxic deaths. The study for previously untreated patients required cyclophosphamide, doxorubicin, and 5-fluorouracil (CAF) after 4 cycles of TMTX. This study design for previously untreated patients allows the Cancer and Leukemia Group B (CALGB) to prospectively evaluate the activity of new agents in "chemotherapy-sensitive" metastatic breast cancer.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=1829134&dopt=Abstract">Link to article in PubMed</a></p>
dc.relation.urlhttps://doi.org/10.1002/mpo.2950190413
dc.subjectAntineoplastic Agents
dc.subjectAntineoplastic Combined Chemotherapy Protocols
dc.subjectBreast Neoplasms
dc.subjectCarcinoma
dc.subjectCyclophosphamide
dc.subjectDoxorubicin
dc.subjectDrug Administration Schedule
dc.subjectFemale
dc.subjectFluorouracil
dc.subjectHematologic Diseases
dc.subjectHumans
dc.subjectLiver Neoplasms
dc.subjectMiddle Aged
dc.subjectQuinazolines
dc.subjectTrimetrexate
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.subjectWomen's Studies
dc.titleTrimetrexate in untreated and previously treated patients with metastatic breast cancer: a Cancer and Leukemia Group B study
dc.typeJournal Article
dc.source.journaltitleMedical and pediatric oncology
dc.source.volume19
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/wfc_pp/99
dc.identifier.contextkey330335
html.description.abstract<p>Twenty-two patients with previously untreated metastatic breast cancer and nineteen patients with refractory metastatic breast cancer were treated with trimetrexate (TMTX). Patients received TMTX 8 mg/m2/day if previously treated or 12 mg/m2/day if previously untreated, both given by intravenous bolus days 1-5, every 21 days. None of the patients previously treated for metastatic disease responded to TMTX. There was one partial responder among the 22 patients with previously untreated metastatic disease. The primary toxicity was hematologic and occurred more frequently in patients with a pleural effusion, low serum protein or albumin, or poor performance status. There were three toxic deaths. The study for previously untreated patients required cyclophosphamide, doxorubicin, and 5-fluorouracil (CAF) after 4 cycles of TMTX. This study design for previously untreated patients allows the Cancer and Leukemia Group B (CALGB) to prospectively evaluate the activity of new agents in "chemotherapy-sensitive" metastatic breast cancer.</p>
dc.identifier.submissionpathwfc_pp/99
dc.contributor.departmentDepartment of Medicine, Division of Hematology/Oncology
dc.source.pages283-8


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