Abstract
The combination of gemcitabine and cisplatin has proven effective as first-line chemotherapy for patients with breast cancer, inducing a response rate of 80% in one phase II study. Five additional studies in intensively pretreated breast cancer patients demonstrated a median response rate of 43% (range, 26%-50%). The toxicity profile was moderate, with thrombocytopenia and neutropenia as the main side effects. The gemcitabine/ cisplatin combination, therefore, offers a tolerable and effective treatment option, particularly for patients whose disease progressed after treatment with anthracyclines and/or taxanes.
MeSH terms
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Anthracyclines
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Antibodies, Monoclonal / administration & dosage
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Antibodies, Monoclonal, Humanized
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
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Breast Neoplasms / drug therapy*
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Breast Neoplasms / pathology
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Bridged-Ring Compounds
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Cisplatin / administration & dosage
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Clinical Trials, Phase II as Topic
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Deoxycytidine / administration & dosage
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Deoxycytidine / analogs & derivatives*
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Female
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Gemcitabine
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Humans
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Neoplasm Metastasis
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Taxoids*
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Trastuzumab
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Treatment Failure
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Treatment Outcome
Substances
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Anthracyclines
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Humanized
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Bridged-Ring Compounds
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Taxoids
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Deoxycytidine
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taxane
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Trastuzumab
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Cisplatin
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Gemcitabine