Source:http://linkedlifedata.com/resource/pubmed/id/17192902
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
6
|
pubmed:dateCreated |
2007-2-5
|
pubmed:abstractText |
We investigated the relationships between genetic factors and clinical outcome in Japanese non-small-cell lung cancer (NSCLC) patients treated with gefitinib. Ninety-eight NSCLC patients who had been treated with gefitinib, were screened for mutations in epidermal growth factor receptor (EGFR) exons 18-21, KRAS exon2, and polymorphisms including the CA simple sequence repeat in intron1 (CA-SSR1) and single nucleotide polymorphisms in the promoter region (-216G/T and -191C/A), using a PCR-based assay and direct sequencing. The EGFR copy number status was also evaluated using a fluorescence in situ hybridization assay. EGFR and KRAS mutations were found in 38 (38.8%) and 8 (8.2%) of the 98 patients, respectively. A high EGFR copy number status was identified in 31 (41.3%) of the 75 assessable patients. Drug-sensitive EGFR mutations limited to exon19 deletions and L858R were independent predictive factors of a stronger sensitivity to gefitinib (p = 0.0002), the overall survival (OS) (p = 0.0036), and prolonged progression-free survival (PFS) (p < 0.0001). The EGFR copy number status was not related to a sensitivity to gefitinib and prolonged OS and PFS. Regarding polymorphisms, patients with a short CA-SSR1 showed a prolonged OS as compared with those with a long length in patients with a drug-sensitive EGFR mutation, although this difference was not significant (p = 0.13). Thus, drug-sensitive EGFR mutations predict a favorable clinical outcome and a high EGFR copy number may not be related to clinical benefits in gefitinib-treated Japanese patients with NSCLC. Our findings also suggest that the CA-SSR1 length may influence the clinical outcome in patients with a drug-sensitive EGFR mutation.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Antineoplastic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/KRAS protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Proto-Oncogene Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Quinazolines,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Epidermal Growth Factor,
http://linkedlifedata.com/resource/pubmed/chemical/gefitinib,
http://linkedlifedata.com/resource/pubmed/chemical/ras Proteins
|
pubmed:status |
MEDLINE
|
pubmed:month |
Mar
|
pubmed:issn |
0020-7136
|
pubmed:author |
pubmed-author:AoeKeisukeK,
pubmed-author:AoeMotoiM,
pubmed-author:AsanoHiroakiH,
pubmed-author:DateHiroshiH,
pubmed-author:FujiwaraYoshiroY,
pubmed-author:HottaKatsuyukiK,
pubmed-author:IchiharaShujiS,
pubmed-author:IchimuraKouichiK,
pubmed-author:KiuraKatsuyukiK,
pubmed-author:ShigematsuHisayukiH,
pubmed-author:ShimizuKenjiK,
pubmed-author:ShimizuNobuyoshiN,
pubmed-author:SohJunichiJ,
pubmed-author:TokumoMasakiM,
pubmed-author:ToyookaShinichiS
|
pubmed:copyrightInfo |
(c) 2006 Wiley-Liss, Inc.
|
pubmed:issnType |
Print
|
pubmed:day |
15
|
pubmed:volume |
120
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
1239-47
|
pubmed:dateRevised |
2009-11-19
|
pubmed:meshHeading |
pubmed-meshheading:17192902-Aged,
pubmed-meshheading:17192902-Antineoplastic Agents,
pubmed-meshheading:17192902-Carcinoma, Non-Small-Cell Lung,
pubmed-meshheading:17192902-Dinucleotide Repeats,
pubmed-meshheading:17192902-Drug Resistance, Neoplasm,
pubmed-meshheading:17192902-Female,
pubmed-meshheading:17192902-Humans,
pubmed-meshheading:17192902-Lung Neoplasms,
pubmed-meshheading:17192902-Male,
pubmed-meshheading:17192902-Mutation,
pubmed-meshheading:17192902-Polymorphism, Genetic,
pubmed-meshheading:17192902-Promoter Regions, Genetic,
pubmed-meshheading:17192902-Proto-Oncogene Proteins,
pubmed-meshheading:17192902-Quinazolines,
pubmed-meshheading:17192902-Receptor, Epidermal Growth Factor,
pubmed-meshheading:17192902-Treatment Outcome,
pubmed-meshheading:17192902-ras Proteins
|
pubmed:year |
2007
|
pubmed:articleTitle |
The impact of epidermal growth factor receptor gene status on gefitinib-treated Japanese patients with non-small-cell lung cancer.
|
pubmed:affiliation |
Department of Cancer and Thoracic Surgery, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences, 2-5-1 Shikata-cho, Okayama 700-8558, Japan.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|