Source:http://linkedlifedata.com/resource/pubmed/id/15746582
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
4
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pubmed:dateCreated |
2005-3-4
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pubmed:abstractText |
We evaluated the efficacy and toxicity of cisplatin, tegafur plus uracil and leucovorin as neoadjuvant chemotherapy for locally advanced squamous cell carcinoma (SCC) of the oropharynx and hypopharynx. Forty-six patients (stage IV, 83%; N2/3, 52%) were treated with PUL (50 mg/m2 cisplatin on day 1, 300 mg/m2 tegafur plus uracil orally and 60 mg leucovorin orally on days 1-14) over a 14-day cycle. Evaluation after 3 cycles led to chemotherapy termination if primary tumor responses were less than partial responses. Otherwise, PUL was continued up to 6 cycles before locoregional therapy. Patients achieving at least good partial responses at the primary site after neoadjuvant chemotherapy received radiotherapy for organ preservation. Chemotherapy responses were analyzed by intent-to-treat. Response rates of primary sites were 71.7% (33 of 46) with 34.8% (16 of 46) showing a complete response. Thirty patients (65.2%) achieved good partial responses at the primary site. Overall response and complete response rates of neck lymph nodes were 68.6% (24 of 35) and 25.7% (nine of 35). The combined response rate of primary site and neck lymph nodes was 63% (95% confidence interval 48.5-77.5%) with a complete response rate of 15.2%. Toxicities of WHO grade 3-4 included anemia (19.6%), diarrhea (17.4%) and neutropenia (8.7%). With a median follow-up of 36 months, overall survival and disease-free survival rates were 45.7% (21 of 46) and 41.3% (19 of 46); organ preservation rate was 90% (19 of 21). We concluded that the outpatient PUL regimen was a moderately effective, less-toxic neoadjuvant chemotherapy for SCC of the oropharynx and hypopharynx. PUL should be studied further with other active agents or radiotherapy.
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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 |
Apr
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pubmed:issn |
0959-4973
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
16
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
447-53
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pubmed:dateRevised |
2006-4-24
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pubmed:meshHeading |
pubmed-meshheading:15746582-Adult,
pubmed-meshheading:15746582-Aged,
pubmed-meshheading:15746582-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:15746582-Carcinoma, Squamous Cell,
pubmed-meshheading:15746582-Cisplatin,
pubmed-meshheading:15746582-Female,
pubmed-meshheading:15746582-Humans,
pubmed-meshheading:15746582-Hypopharyngeal Neoplasms,
pubmed-meshheading:15746582-Leucovorin,
pubmed-meshheading:15746582-Male,
pubmed-meshheading:15746582-Maximum Tolerated Dose,
pubmed-meshheading:15746582-Middle Aged,
pubmed-meshheading:15746582-Neoadjuvant Therapy,
pubmed-meshheading:15746582-Neoplasm Staging,
pubmed-meshheading:15746582-Oropharyngeal Neoplasms,
pubmed-meshheading:15746582-Survival Rate,
pubmed-meshheading:15746582-Tegafur,
pubmed-meshheading:15746582-Uracil
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pubmed:year |
2005
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pubmed:articleTitle |
Phase II trial of cisplatin, tegafur plus uracil and leucovorin as neoadjuvant chemotherapy in patients with squamous cell carcinoma of the oropharynx and hypopharynx.
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pubmed:affiliation |
Division of Hematology/Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital, Taipei, Taiwan. whm526@ms12.hinet.net
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Clinical Trial, Phase II
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