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Erschienen in: Tumor Biology 3/2012

01.06.2012 | Research Article

Pharmacogenetic role of ERCC1 genetic variants in treatment response of platinum-based chemotherapy among advanced non-small cell lung cancer patients

verfasst von: Dianke Yu, Juan Shi, Tong Sun, Xiaoli Du, Li Liu, Xiaojiao Zhang, Chao Lu, Xiaohu Tang, Meng Li, Lingchen Xiao, Zhouwei Zhang, Qipeng Yuan, Ming Yang

Erschienen in: Tumor Biology | Ausgabe 3/2012

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Abstract

The excision repair cross-complementation group 1 (ERCC1) plays an essential role in DNA repair and has been linked to resistance to platinum-based anticancer drugs among advanced non-small cell lung cancer (NSCLC) patients. We systematically evaluate whether ERCC1 Asn118Asn and C8092A genetic variants are associated with treatment response of platinum chemotherapy. We preformed a meta-analysis using ten eligible cohort studies (including 11 datasets) with a total of 1,252 NSCLC patients to summarize the existing data on the association between the ERCC1 Asn118Asn and C8092A polymorphisms and response to platinum regiments. Odds ratio or hazard ratio with 95% confidence interval were calculated to estimate the correlation. We found that neither ERCC1 C8092A polymorphism nor Asn118Asn variant is associated with different response of platinum-based treatment among advanced NSCLC patients. Additionally, these two genetic variants are not related to treatment response in either Caucasian patients or Asian patients. Our meta-analysis indicates that the ERCC1 Asn118Asn and C8092A polymorphisms may not be good prognostic biomarkers for platinum-based chemotherapy in patients with stage III–IV NSCLC.
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Metadaten
Titel
Pharmacogenetic role of ERCC1 genetic variants in treatment response of platinum-based chemotherapy among advanced non-small cell lung cancer patients
verfasst von
Dianke Yu
Juan Shi
Tong Sun
Xiaoli Du
Li Liu
Xiaojiao Zhang
Chao Lu
Xiaohu Tang
Meng Li
Lingchen Xiao
Zhouwei Zhang
Qipeng Yuan
Ming Yang
Publikationsdatum
01.06.2012
Verlag
Springer Netherlands
Erschienen in
Tumor Biology / Ausgabe 3/2012
Print ISSN: 1010-4283
Elektronische ISSN: 1423-0380
DOI
https://doi.org/10.1007/s13277-011-0314-y

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