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印度南部结直肠癌(CRC)患者 ABCB-1、ERCC-1 和 ERCC-2 基因多态性对卡培他滨和奥沙利铂(CAPOX)治疗反应的影响。

Influence of ABCB-1, ERCC-1 and ERCC-2 gene polymorphisms on response to capecitabine and oxaliplatin (CAPOX) treatment in colorectal cancer (CRC) patients of South India.

机构信息

Pharmacology Department, JIPMER, Puducherry, India.

Regional Cancer Centre, JIPMER, Puducherry, India.

出版信息

J Clin Pharm Ther. 2020 Aug;45(4):617-627. doi: 10.1111/jcpt.13166. Epub 2020 May 12.

Abstract

WHAT IS KNOWN AND OBJECTIVE

High interindividual response variability was reported with capecitabine and oxaliplatin (CAPOX) regimen in colorectal cancer (CRC). The single nucleotide polymorphisms (SNPs) of the genes related to drug efflux transport (ABCB1) and DNA repair (ERCC) could result in altered tumour response. Hence, this study was designed to assess the influence of ABCB1, ERCC-1 and ERCC-2 gene polymorphisms on tumour response to CAPOX treatment in CRC patients of South Indian origin.

PATIENTS AND METHODS

A total of 145 newly diagnosed CRC patients were included in the final analysis. Response to CAPOX treatment in the adjuvant setting was assessed in terms of disease-free survival rate (DFSR) and overall survival rate (OSR) at 3 years, whereas in the palliative setting, the response was assessed as progression-free survival rate (PFSR) and OSR at 3 years. Five millilitres of the venous blood sample was collected from each patient for genomic DNA extraction by the manual phenol-chloroform method. Genotyping and allelic discrimination analysis were done using real-time PCR (RT-PCR).

RESULTS AND DISCUSSION

With ABCB1 gene polymorphism rs1045642 (A > G), patients with AG/GG genotype showed better DFSR [P value = .02, OR = 2 (CI: 1.5-3)] and PFSR [P value = .02, OR = 1.6 (CI: 1.1-2.5)] when compared to AA genotype in the adjuvant and palliative settings, respectively. Similarly with rs1128503 (A > G) polymorphism, patients with AG/GG genotype were found to have better DFSR [P value = .02, OR = 1.9 (CI: 1.3-3)] and PFSR [P value = .01, OR = 2 (CI: 1.1-3.7)] when compared to AA genotype. However, we did not find any association between CAPOX response and ABCB1 gene polymorphisms in a binary logistic regression when non-genetic predictors were considered for analysis. We did not find any association with ERCC1 (rs11615 A > G) and ERCC2 (rs13181 T > G) gene polymorphisms with respect to CAPOX response in either of the treatment settings.

WHAT IS NEW AND CONCLUSION

The response to CAPOX treatment was found to be influenced by the ABCB1 gene variants (rs1128503 and rs1045642), thereby strengthening their predictive role. No association was found between ERCC1 (rs11615 A > G), ERCC2 (rs13181 T > G) gene polymorphisms and tumour response to CAPOX treatment in CRC patients of South Indian origin.

摘要

已知和目的

卡培他滨和奥沙利铂(CAPOX)方案在结直肠癌(CRC)患者中表现出高度的个体间反应变异性。与药物外排转运(ABCB1)和 DNA 修复(ERCC)相关的基因的单核苷酸多态性(SNP)可能导致肿瘤反应改变。因此,本研究旨在评估 ABCB1、ERCC-1 和 ERCC-2 基因多态性对南印度 CRC 患者 CAPOX 治疗肿瘤反应的影响。

患者和方法

共纳入 145 例新诊断的 CRC 患者进行最终分析。在辅助治疗中,根据无病生存率(DFSR)和 3 年总生存率(OSR)评估 CAPOX 治疗的反应,而在姑息治疗中,根据无进展生存率(PFSR)和 3 年 OSR 评估反应。从每位患者采集 5 毫升静脉血样,通过手动酚氯仿法提取基因组 DNA。使用实时 PCR(RT-PCR)进行基因分型和等位基因鉴别分析。

结果与讨论

ABCB1 基因多态性 rs1045642(A>G)中,与 AA 基因型相比,AG/GG 基因型的患者在辅助和姑息治疗中均具有更好的 DFSR [P 值=.02,OR=2(CI:1.5-3)]和 PFSR [P 值=.02,OR=1.6(CI:1.1-2.5)]。同样,rs1128503(A>G)多态性中,与 AA 基因型相比,AG/GG 基因型的患者具有更好的 DFSR [P 值=.02,OR=1.9(CI:1.3-3)]和 PFSR [P 值=.01,OR=2(CI:1.1-3.7)]。然而,当考虑非遗传预测因素进行分析时,我们在二元逻辑回归中未发现 CAPOX 反应与 ABCB1 基因多态性之间存在任何关联。在两种治疗方案中,我们均未发现 ERCC1(rs11615 A>G)和 ERCC2(rs13181 T>G)基因多态性与 CAPOX 反应之间存在任何关联。

新发现和结论

CAPOX 治疗的反应受 ABCB1 基因变异(rs1128503 和 rs1045642)的影响,从而增强了其预测作用。在南印度 CRC 患者中,未发现 ERCC1(rs11615 A>G)、ERCC2(rs13181 T>G)基因多态性与 CAPOX 治疗肿瘤反应之间存在任何关联。

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