Source:http://linkedlifedata.com/resource/pubmed/id/20143185
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2011-2-25
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pubmed:abstractText |
The published data on the predictive value of polymorphism of ERCC1 and XPD in patients with advanced non-small cell lung cancer receiving platinum-based chemotherapy are inconclusive. To derive a more precise estimation of the relationship, a meta-analysis was performed. Relevant studies were identified by searching the Medline, Embase, CNKI and American Society of Clinical Oncology abstract databases. Inclusion criteria were patients with advanced NSCLC, received platinum-based chemotherapy, evaluation of polymorphism of ERCC1 and XPD and overall response rate (ORR). A total of 12 studies were included in this meta-analysis. For studies evaluating ERCC1 polymorphism at codon 118, the ORR for the wild-type C/C genotype versus the heterozygous C/T and T/T genotype was 2.17 (95% confidence interval (CI), 1.43-3.33; P = 0.000). For studies evaluating XPD Asp312Asn and XPD Lys751Gln, the pooled OR was 1.33 (95% CI, 0.92-1.91; P = 0.13) and 1.02 (95% CI, 0.72-1.45; P = 0.915), respectively. The results indicated that platinum-based chemotherapy sensitivity was significantly associated with polymorphism of ERCC1 C118T. However, XPD Asp312Asn and XPD Lys751Gln were not predictive makers for platinum-based chemotherapy in patients with advanced NSCLC.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Carboplatin,
http://linkedlifedata.com/resource/pubmed/chemical/Cisplatin,
http://linkedlifedata.com/resource/pubmed/chemical/DNA-Binding Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/ERCC1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/ERCC2 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Endonucleases,
http://linkedlifedata.com/resource/pubmed/chemical/Xeroderma Pigmentosum Group D...
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
1559-131X
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
28
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
315-21
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pubmed:meshHeading |
pubmed-meshheading:20143185-Antineoplastic Combined Chemotherapy Protocols,
pubmed-meshheading:20143185-Carboplatin,
pubmed-meshheading:20143185-Carcinoma, Non-Small-Cell Lung,
pubmed-meshheading:20143185-Cisplatin,
pubmed-meshheading:20143185-DNA-Binding Proteins,
pubmed-meshheading:20143185-Endonucleases,
pubmed-meshheading:20143185-Humans,
pubmed-meshheading:20143185-Lung Neoplasms,
pubmed-meshheading:20143185-Meta-Analysis as Topic,
pubmed-meshheading:20143185-Polymorphism, Genetic,
pubmed-meshheading:20143185-Prognosis,
pubmed-meshheading:20143185-Xeroderma Pigmentosum Group D Protein
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pubmed:year |
2011
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pubmed:articleTitle |
Predictive value of ERCC1 and XPD polymorphism in patients with advanced non-small cell lung cancer receiving platinum-based chemotherapy: a systematic review and meta-analysis.
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pubmed:affiliation |
Department of Respiratory Medicine, Jinling Hospital, Nanjing University School of Medicine, 305 East Zhongshan Road, 210002 Nanjing, China.
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pubmed:publicationType |
Journal Article,
Review
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