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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
3
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pubmed:dateCreated |
1995-5-18
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pubmed:abstractText |
A combination chemotherapy consisting of a 72-hour continuous infusion of cisplatin (CDDP; 100 mg/m2/72 h) and 5-fluorouracil (5-FU; 3 g/m2/72 h) was conducted for inoperable non-small cell lung cancer (NSCLC). Sixty patients were accepted for this study between June 1988 and December 1990. Forty-seven patients were male (median age 68). Thirty-four patients had stage III and 26 had stage IV disease. The response rate was 25.0% (95% confidence interval, CI, 14.0-36.0%), median survival was 15.7 months. In squamous cell carcinoma, the response rate was 35.5% (95% CI, 18.7-52.3%) and median survival was 15.1 months. In non-squamous cell carcinoma, the response rate was 13.8% (95% CI, 1.2-26.4%) and median survival was 17.7 months. There was a significant difference in response rate (p < 0.01), but no significant difference in survival (p = 0.36). Grade 3 leukopenia was 11.7%, grade 3 and 4 thrombocytopenia was 13.3%. Grade 3 nausea and vomiting were 8.3%. One patient had grade 4 renal toxicity. However, there was no treatment-related death. This regimen was well tolerated. In multivariate analysis, the significant parameters were CEA, performance status and response. In conclusion, 72-hour continuous infusion of CDDP and 5-FU for treatment of NSCLC provides similar response and toxicity as previously reported regimens using CDDP.
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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:issn |
0030-2414
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
52
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pubmed:owner |
NLM
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pubmed:authorsComplete |
N
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pubmed:pagination |
246-50
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pubmed:dateRevised |
2006-4-24
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pubmed:meshHeading |
pubmed-meshheading:7715909-Adult,
pubmed-meshheading:7715909-Aged,
pubmed-meshheading:7715909-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:7715909-Carcinoma, Non-Small-Cell Lung,
pubmed-meshheading:7715909-Cisplatin,
pubmed-meshheading:7715909-Drug Administration Schedule,
pubmed-meshheading:7715909-Female,
pubmed-meshheading:7715909-Fluorouracil,
pubmed-meshheading:7715909-Humans,
pubmed-meshheading:7715909-Infusions, Intravenous,
pubmed-meshheading:7715909-Lung Neoplasms,
pubmed-meshheading:7715909-Male,
pubmed-meshheading:7715909-Middle Aged,
pubmed-meshheading:7715909-Prognosis,
pubmed-meshheading:7715909-Proportional Hazards Models,
pubmed-meshheading:7715909-Survival Analysis,
pubmed-meshheading:7715909-Treatment Outcome
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pubmed:articleTitle |
A phase II study of 72-hour continuous infusion consisting of cisplatin and 5-fluorouracil for treatment of non-small cell lung cancer.
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pubmed:affiliation |
National Nishi-Gunma Hospital, Japan.
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Clinical Trial, Phase II
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