Study on ERCC1,XPD and XPA polymorphisms for prediction of platinum-based chemotherapy sensitivity in non-small cell lung cancer
Yitian Chen
Abstract
Yitian Chen
Abstract
OBJECTIVE:To analyze the correlations between genetic polymorphisms of ERCC1Asn118Asn,XPD Lys751Gln,XPA A23G and the clinical benefits to the platinum-based chemotherapy in NSCLC,and further investigate the effect of different genotypes for the survival and clinical outcome.METHODS:The polymerase chain reaction-restrictive fragment length polymorphism(PCR-RFLP)method was applied to measure the genotype in 94 patients with NSCLC,and the correlations of genetic polymorphisms with clinical benefits and survival were analyzed.RESULTS:The distributions of XPD genotypes differed significantly in median survival time(MST)(χ2=7.353,P=0.007),Lys/Lys was 11 months,while Lys/Gln and Gln/Gln was 12 months(95%CI:9.94-12.06,11.21-12.79,respectively),but there were no significant differences in clinical benefits to platinum-based chemotherapy,χ2=2.604,P=0.272.The same statistical results were found between the genetic polymorphisms and clinical benefits on ERCC1Asn118Asn and XPA A23G(χ2=0.451,P=1.000;χ2=1.383,P=0.550;respectively).The heterozygous genotypes of XPA and ERCC1 were not detected.CONCLUSION:XPD Lys751Gln genetic polymorphisms may be an important marker for prediction the survival in NSCLC,and can provide theoretical basis for individualized treatment.
OpenAlex reports 6 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
OBJECTIVE:To analyze the correlations between genetic polymorphisms of ERCC1Asn118Asn,XPD Lys751Gln,XPA A23G and the clinical benefits to the platinum-based chemotherapy in NSCLC,and further investigate the effect of different genotypes for the survival and clinical outcome.METHODS:The polymerase chain reaction-restrictive fragment length polymorphism(PCR-RFLP)method was applied to measure the genotype in 94 patients with NSCLC,and the correlations of genetic polymorphisms with clinical benefits and survival were analyzed.RESULTS:The distributions of XPD genotypes differed significantly in median survival time(MST)(χ2=7.353,P=0.007),Lys/Lys was 11 months,while Lys/Gln and Gln/Gln was 12 months(95%CI:9.94-12.06,11.21-12.79,respectively),but there were no significant differences in clinical benefits to platinum-based chemotherapy,χ2=2.604,P=0.272.The same statistical results were found between the genetic polymorphisms and clinical benefits on ERCC1Asn118Asn and XPA A23G(χ2=0.451,P=1.000;χ2=1.383,P=0.550;respectively).The heterozygous genotypes of XPA and ERCC1 were not detected.CONCLUSION:XPD Lys751Gln genetic polymorphisms may be an important marker for prediction the survival in NSCLC,and can provide theoretical basis for individualized treatment.
Key concepts: ERCC1, Genotype, Lung cancer, Chemotherapy, Oncology, Internal medicine, Biology, Polymerase chain reaction