Source:http://linkedlifedata.com/resource/pubmed/id/16759850
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rdf:type | |
lifeskim:mentions |
umls-concept:C0006826,
umls-concept:C0007131,
umls-concept:C0008838,
umls-concept:C0013216,
umls-concept:C0029246,
umls-concept:C0030705,
umls-concept:C0035168,
umls-concept:C0087111,
umls-concept:C0205263,
umls-concept:C0239307,
umls-concept:C0246415,
umls-concept:C0282460,
umls-concept:C0456598,
umls-concept:C1516985
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pubmed:issue |
10
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pubmed:dateCreated |
2006-6-20
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pubmed:abstractText |
The objective of this phase II study was to document activity and toxicity of docetaxel and cisplatin as induction chemotherapy in patients with stage IIIA N2 non-small cell lung cancer (NSCLC) before definitive local treatment. Forty-six chemotherapy-nai ve patients (median age 60 years) were included. Treatment consisted of 3 cycles of docetaxel (85 mg/m2 on day 1), followed by cisplatin (40 mg/m2/day on days 1 and 2) every 21 days. Grade 3-4 leukopenia and neutropenia occurred in 45.7% and 65.2% of the patients, respectively. Among 8 cases of febrile neutropenia (17.4%), one (2.2%) resulted in early death. Common grade 3-4 non-haematological toxicities were nausea (17.4%) and vomiting (13%). Eighty-five percent of the patients received three courses; six stopped prematurely due to toxicity, one due to protocol violation. Response rate was the primary endpoint of this study. Considering eligible patients (n=40), 18 responses (1 complete and 17 partial responses) were observed (response rate 45%; 95% Confidence interval (CI): 29.3%-61.5%). In stage IIIA-N2 NSCLC patients, docetaxel-cisplatin could be administered and demonstrated manageable toxicity with modest efficacy.
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pubmed:grant | |
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 |
Jul
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pubmed:issn |
0959-8049
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
42
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
1399-406
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
pubmed-meshheading:16759850-Adult,
pubmed-meshheading:16759850-Aged,
pubmed-meshheading:16759850-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:16759850-Carcinoma, Non-Small-Cell Lung,
pubmed-meshheading:16759850-Cisplatin,
pubmed-meshheading:16759850-Disease-Free Survival,
pubmed-meshheading:16759850-Female,
pubmed-meshheading:16759850-Humans,
pubmed-meshheading:16759850-Lung Neoplasms,
pubmed-meshheading:16759850-Male,
pubmed-meshheading:16759850-Middle Aged,
pubmed-meshheading:16759850-Remission Induction,
pubmed-meshheading:16759850-Survival Analysis,
pubmed-meshheading:16759850-Taxoids,
pubmed-meshheading:16759850-Treatment Outcome
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pubmed:year |
2006
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pubmed:articleTitle |
Docetaxel and cisplatin as induction chemotherapy in patients with pathologically-proven stage IIIA N2 non-small cell lung cancer: a phase II study of the European organization for research and treatment of cancer (EORTC 08984).
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pubmed:affiliation |
Afdeling Longziekten, Jeroen Bosch Ziekenhuis, Nieuwstraat 34, 5211 NL's-Hertogenbosch, The Netherlands. b.biesma@jbz.nl
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't,
Multicenter Study,
Clinical Trial, Phase II,
Research Support, N.I.H., Extramural
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