Source:http://linkedlifedata.com/resource/pubmed/id/15298734
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
8
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pubmed:dateCreated |
2004-8-9
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pubmed:abstractText |
To determine the recommended phase II dose of vinorelbine in combination with cisplatin and thoracic radiotherapy (TRT) in patients with unresectable stage III non-small cell lung cancer (NSCLC), 18 patients received cisplatin (80 mg/m2) on day 1 and vinorelbine (20 mg/m2 in level 1, and 25 mg/m2 in level 2) on days 1 and 8 every 4 weeks for 4 cycles. TRT consisted of a single dose of 2 Gy once daily for 3 weeks followed by a rest of 4 days, and then the same TRT for 3 weeks to a total dose of 60 Gy. Fifteen (83%) patients received 60 Gy of TRT and 14 (78%) patients received 4 cycles of chemotherapy. Ten (77%) of 13 patients at level 1 and all 5 patients at level 2 developed grade 3-4 neutropenia. Four (31%) patients at level 1 and 3 (60%) patients at level 2 developed grade 3-4 infection. None developed > or = grade 3 esophagitis or lung toxicity. Dose-limiting toxicity was noted in 33% of the patients in level 1 and in 60% of the patients in level 2. The overall response rate (95% confidence interval) was 83% (59-96%) with 15 partial responses. The median survival time was 30.4 months, and the 1-year, 2-year, and 3-year survival rates were 72%, 61%, and 50%, respectively. In conclusion, the recommended dose is the level 1 dose, and this regimen is feasible and promising in patients with stage III NSCLC.
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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 |
Aug
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pubmed:issn |
1347-9032
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pubmed:author |
pubmed-author:KodamaTetsuroT,
pubmed-author:KunitohHideoH,
pubmed-author:NodaKazumasaK,
pubmed-author:NokiharaHiroshiH,
pubmed-author:OheYuichiroY,
pubmed-author:OshitaFumihiroF,
pubmed-author:SaijoNagahiroN,
pubmed-author:SekineIkuoI,
pubmed-author:SumiMinakoM,
pubmed-author:TamuraTomohideT,
pubmed-author:TanakaManabuM,
pubmed-author:YamadaKouzouK,
pubmed-author:YamamotoNoboruN,
pubmed-author:YamashitaKosukeK
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pubmed:issnType |
Print
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pubmed:volume |
95
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
691-5
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pubmed:dateRevised |
2006-4-24
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pubmed:meshHeading |
pubmed-meshheading:15298734-Adult,
pubmed-meshheading:15298734-Aged,
pubmed-meshheading:15298734-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:15298734-Carcinoma, Non-Small-Cell Lung,
pubmed-meshheading:15298734-Cisplatin,
pubmed-meshheading:15298734-Female,
pubmed-meshheading:15298734-Humans,
pubmed-meshheading:15298734-Infusions, Intravenous,
pubmed-meshheading:15298734-Lung Neoplasms,
pubmed-meshheading:15298734-Male,
pubmed-meshheading:15298734-Maximum Tolerated Dose,
pubmed-meshheading:15298734-Middle Aged,
pubmed-meshheading:15298734-Survival Analysis,
pubmed-meshheading:15298734-Vinblastine
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pubmed:year |
2004
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pubmed:articleTitle |
Phase I study of cisplatin, vinorelbine, and concurrent thoracic radiotherapy for unresectable stage III non-small cell lung cancer.
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pubmed:affiliation |
Division of Thoracic Oncology, National Cancer Center Hospital, Chuo-ku, Tokyo 104-0045, Japan. isekine@ncc.go.jp
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Clinical Trial, Phase I
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