Source:http://linkedlifedata.com/resource/pubmed/id/11804695
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
2
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pubmed:dateCreated |
2002-1-23
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pubmed:abstractText |
Weekly administration of low-dose taxane reduces myelosuppression and increases dose intensity as compared with an every third week schedule. We conducted a phase II trial of weekly docetaxel and cisplatin in patients with advanced non-small cell lung cancer (NSCLC) to evaluate safety and efficacy. Thirty-seven patients with chemonaïve stage IIIB (n=15), stage IV (n=16), or recurrence after operation (n=6) NSCLC received intravenous infusions of docetaxel at 35 mg/m(2) and cisplatin at 25 mg/m(2) for three consecutive weeks, followed by a week of rest. There were ten partial responses for an objective response rate of 30% (95% confidence interval (CI), 15-46%) in 33 evaluable patients and 27% (95% CI, 13-41%) in the intent-to-treatment population. The median survival was 12.8 months (range 2.5-17.1), and the 1-year survival was 54%. Hematologic toxicities, which were mild, included grade 4 neutropenia in 6%. There were none with febrile neutropenia or severe (grade 3-4) infections, and no septic deaths. The common nonhematologic toxicities included grade 2-3 nausea and vomiting (44%) and grade 2-3 diarrhea (14%). Consecutive weekly administrations of docetaxel and cisplatin for 3 weeks produces minimal myelosuppression and shows activity in the treatment of chemonaïve patients with advanced NSCLC. A randomized phase III trial is warranted to compare this 3 consecutive weeks protocol with administration of docetaxel and cisplatin every third week.
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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 |
Feb
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pubmed:issn |
0169-5002
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
35
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
209-14
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pubmed:dateRevised |
2006-11-15
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pubmed:meshHeading |
pubmed-meshheading:11804695-Adult,
pubmed-meshheading:11804695-Aged,
pubmed-meshheading:11804695-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:11804695-Carcinoma, Non-Small-Cell Lung,
pubmed-meshheading:11804695-Cisplatin,
pubmed-meshheading:11804695-Drug Administration Schedule,
pubmed-meshheading:11804695-Female,
pubmed-meshheading:11804695-Humans,
pubmed-meshheading:11804695-Infusions, Intravenous,
pubmed-meshheading:11804695-Lung Neoplasms,
pubmed-meshheading:11804695-Male,
pubmed-meshheading:11804695-Middle Aged,
pubmed-meshheading:11804695-Neutropenia,
pubmed-meshheading:11804695-Paclitaxel,
pubmed-meshheading:11804695-Survival Analysis,
pubmed-meshheading:11804695-Taxoids,
pubmed-meshheading:11804695-Treatment Outcome
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pubmed:year |
2002
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pubmed:articleTitle |
Phase II study of docetaxel and cisplatin administered as three consecutive weekly infusions for advanced non-small cell lung cancer.
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pubmed:affiliation |
Division of Thoracic Oncology, National Cancer Center Hospital East, 6-5-1 Kashiwanoha, Kashiwa, Chiba 277-8577, Japan. siniho@east.ncc.go.jp
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pubmed:publicationType |
Journal Article,
Clinical Trial,
Research Support, Non-U.S. Gov't,
Clinical Trial, Phase II
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