Source:http://linkedlifedata.com/resource/pubmed/id/18418220
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rdf:type | |
lifeskim:mentions |
umls-concept:C0006826,
umls-concept:C0013216,
umls-concept:C0030705,
umls-concept:C0036525,
umls-concept:C0069717,
umls-concept:C0205179,
umls-concept:C0205195,
umls-concept:C0239308,
umls-concept:C0246415,
umls-concept:C0282460,
umls-concept:C0679246,
umls-concept:C0679729,
umls-concept:C1274040,
umls-concept:C1517927,
umls-concept:C1518578,
umls-concept:C1522484,
umls-concept:C2603343
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pubmed:issue |
5
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pubmed:dateCreated |
2008-4-17
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pubmed:abstractText |
A phase II trial was performed to determine the efficacy and tolerance of docetaxel plus oxaliplatin with hematopoietic growth factor support in previously untreated patients with advanced gastroesophageal adenocarcinoma. Thirty-five patients were entered in this trial. Treatment consisted of 3-weekly docetaxel 80 mg/m2 and oxaliplatin 100 mg/m2 both infused on day 1. A prophylactic 5-day course of human granulocyte colony-stimulating factor 5 microg/kg/day was given subcutaneously, and erythropoietin (10,000 IU subcutaneously three times per week) was administered if hemoglobin was less than 12.0 mg/dl. The confirmed overall response rate was 34%, including two complete responses (6%) and 10 partial responses (28%). Fifteen patients (43%) had stable disease. The median time to response was 2.5 months (1-3.5), the median time to progression was 8.9 (4-42.5) months and the median overall survival time was 11.6 (2.5-51) months. Hematologic toxicity was common, though World Health Organization grade 3 or 4 neutropenia occurred only in six (17%) patients and anemia in six (17%) patients, respectively. Nonhematologic adverse reactions were usually mild-to-moderate. Our data suggest that the combination of docetaxel and oxaliplatin with granulocyte colony-stimulating factor and erythropoietin has a promising therapeutic index in patients with advanced gastroesophageal adenocarcinoma.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Erythropoietin,
http://linkedlifedata.com/resource/pubmed/chemical/Granulocyte Colony-Stimulating...,
http://linkedlifedata.com/resource/pubmed/chemical/Organoplatinum Compounds,
http://linkedlifedata.com/resource/pubmed/chemical/Taxoids,
http://linkedlifedata.com/resource/pubmed/chemical/docetaxel,
http://linkedlifedata.com/resource/pubmed/chemical/oxaliplatin
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pubmed:status |
MEDLINE
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pubmed:month |
Jun
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pubmed:issn |
0959-4973
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
19
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
535-9
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pubmed:meshHeading |
pubmed-meshheading:18418220-Adenocarcinoma,
pubmed-meshheading:18418220-Adult,
pubmed-meshheading:18418220-Aged,
pubmed-meshheading:18418220-Anemia,
pubmed-meshheading:18418220-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:18418220-Drug Administration Schedule,
pubmed-meshheading:18418220-Erythropoietin,
pubmed-meshheading:18418220-Esophageal Neoplasms,
pubmed-meshheading:18418220-Female,
pubmed-meshheading:18418220-Granulocyte Colony-Stimulating Factor,
pubmed-meshheading:18418220-Humans,
pubmed-meshheading:18418220-Infusions, Intravenous,
pubmed-meshheading:18418220-Injections, Subcutaneous,
pubmed-meshheading:18418220-Male,
pubmed-meshheading:18418220-Middle Aged,
pubmed-meshheading:18418220-Neutropenia,
pubmed-meshheading:18418220-Organoplatinum Compounds,
pubmed-meshheading:18418220-Stomach Neoplasms,
pubmed-meshheading:18418220-Survival Rate,
pubmed-meshheading:18418220-Taxoids
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pubmed:year |
2008
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pubmed:articleTitle |
Phase II study of docetaxel in combination with oxaliplatin in patients with metastatic or locally advanced esophagogastric cancer previously untreated with chemotherapy for advanced disease: results of the Central European Cooperative Oncology Group Study ESGAS.1.2.001.
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pubmed:affiliation |
Department of Internal Medicine I, Division of Oncology, Medical University of Vienna, Vienna, Austria. michael.hejna@meduniwien.ac.at
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pubmed:publicationType |
Journal Article,
Clinical Trial, Phase II
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