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    Trimetrexate in untreated and previously treated patients with metastatic breast cancer: a Cancer and Leukemia Group B study

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    Authors
    Dawson, N. A.
    Costanza, Mary E.
    Korzun, A. H.
    Clamon, G. H.
    Pollak, M.
    Vogelzang, N. J.
    Carey, R. W.
    Norton, L.
    UMass Chan Affiliations
    Department of Medicine, Division of Hematology/Oncology
    Document Type
    Journal Article
    Publication Date
    1991-01-01
    Keywords
    Antineoplastic Agents
    Antineoplastic Combined Chemotherapy Protocols
    Breast Neoplasms
    Carcinoma
    Cyclophosphamide
    Doxorubicin
    Drug Administration Schedule
    Female
    Fluorouracil
    Hematologic Diseases
    Humans
    Liver Neoplasms
    Middle Aged
    Quinazolines
    Trimetrexate
    Life Sciences
    Medicine and Health Sciences
    Women's Studies
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    Link to Full Text
    https://doi.org/10.1002/mpo.2950190413
    Abstract
    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.
    Source

    Med Pediatr Oncol. 1991;19(4):283-8.

    DOI
    10.1002/mpo.2950190413
    Permanent Link to this Item
    http://hdl.handle.net/20.500.14038/51084
    PubMed ID
    1829134
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    Link to article in PubMed

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    10.1002/mpo.2950190413
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