Source:http://linkedlifedata.com/resource/pubmed/id/15585071
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
5
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pubmed:dateCreated |
2004-12-8
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pubmed:abstractText |
Combined determination of urokinase-type plasminogen activator (uPA) and its inhibitor, activator inhibitor type 1 (PAI-1), supports risk-adapted individualized therapy concepts, particularly in node-negative breast cancer. The prognostic impact of both factors in primary breast cancer was substantiated by a pooled analysis of > 8000 patients with breast cancer and a multicenter prospective randomized therapy trial in node-negative breast cancer; findings achieved the highest level of evidence for tumor biomarkers. Patients with node-negative breast cancer with low antigen levels of uPA and PAI-1 in their primary tumor tissue have a very good prognosis and therefore may be spared the burden of adjuvant chemotherapy, whereas those with elevated uPA/PAI-1 antigen levels carry an increased risk of disease recurrence. Recent retrospective analysis of > 3000 patients indicated that patients with breast cancer with high uPA/PAI-1 values derive a significantly greater benefit from adjuvant chemotherapy than patients with low uPA/PAI-1 levels. Similarly, in the multicenter prospective Chemo N0 trial, administration of cyclophosphamide/methotrexate/5-fluorouracil-based chemotherapy led to a substantial reduction in risk of disease recurrence in patients with high uPA/PAI-1. However, benefit from adjuvant endocrine therapy appears to be independent of a patient's uPA/PAI-1 status. In metastatic breast cancer, retrospective studies showed that elevated uPA or PAI-1 present in the primary tumor tissue are associated with a poor response to later palliative endocrine therapy. These findings suggest that high levels of uPA and/or PAI-1 do reflect an aggressive phenotype that may be overcome or suppressed by early systemic therapy in the adjuvant setting but may be too advanced for response to palliative therapy at a later stage.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Dec
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pubmed:issn |
1526-8209
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
5
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
348-52
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pubmed:dateRevised |
2008-11-21
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pubmed:meshHeading |
pubmed-meshheading:15585071-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:15585071-Breast Neoplasms,
pubmed-meshheading:15585071-Enzyme-Linked Immunosorbent Assay,
pubmed-meshheading:15585071-Female,
pubmed-meshheading:15585071-Humans,
pubmed-meshheading:15585071-Neoadjuvant Therapy,
pubmed-meshheading:15585071-Plasminogen Activator Inhibitor 1,
pubmed-meshheading:15585071-Prognosis,
pubmed-meshheading:15585071-Randomized Controlled Trials as Topic,
pubmed-meshheading:15585071-Treatment Outcome,
pubmed-meshheading:15585071-Urokinase-Type Plasminogen Activator
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pubmed:year |
2004
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pubmed:articleTitle |
Urokinase-type plasminogen activator and its inhibitor type 1 predict disease outcome and therapy response in primary breast cancer.
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pubmed:affiliation |
Department of Obstetrics and Gynecology, Technical University of Munich, Germany. nadia.harbeck@lrz.tum.de
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pubmed:publicationType |
Journal Article,
Review,
Research Support, Non-U.S. Gov't
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