GSTs 基因多态性对晚期非小细胞肺癌患者治疗效果的潜在预测作用。

IF 0.2 Q4 MEDICINE, RESEARCH & EXPERIMENTAL International journal of clinical and experimental medicine Pub Date : 2015-11-15 eCollection Date: 2015-01-01
Kaixiong Liu, Qichang Lin, Haibo Ding, Yongxu Jin, Gongping Chen
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引用次数: 0

摘要

本研究旨在探讨GSTP1、GSTM1和GSTT1多态性与晚期NSCLC治疗结果之间可能存在的关联。研究纳入了 2009 年 10 月至 2011 年 10 月间接受顺铂化疗的 308 例 IIIA、IIIB 或 IV 期 NSCLC 患者。采用聚合酶链式反应-限制性片段长度多态性对 GSTP1、GSTM1 和 GSTT1 多态性进行基因分型。我们发现,与 IIe/IIe 基因型相比,GSTP1 的 IIe/Val 和 Val/Val 基因型对晚期 NSCLC 化疗的 CR+PR 更多,Ors(95% CI)分别为 0.37(0.18-0.71)和 0.15(0.07-0.38)。与IIe/IIe基因型相比,GSTP1的IIe/Val和Val/Val基因型与更长的晚期NSCLC总生存期相关(IIe/Val vs IIe/IIe,37.63 ± 2.01个月 vs 30.25 ± 2.06个月;Val/Val vs IIe/IIe,39.84 ± 3.36个月 vs 30.25 ± 2.06个月)。在Cox比例危险模型中,IIe/Val和Val/Val基因型可显著降低晚期NSCLC患者死于各种原因的风险,HRs(95% CIs)分别为0.51(0.28-0.94)和0.35(0.16-0.78)。我们发现,GSTP1多态性可能会影响晚期NSCLC患者的临床预后,我们的研究结果有助于促进个体化治疗决策。
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Predictive potential role of GSTs gene polymorphisms in the treatment outcome of advanced non-small cell lung cancer patients.

This study aimed to investigate the possible association between GSTP1, GSTM1, and GSTT1 polymorphisms and treatment outcome of advanced NSCLC. Between October 2009 and October 2011, a total of 308 patients of NSCLC on stage IIIA, IIIB or IV, treated with cisplatin-based chemotherapy were included. Polymerase chain reaction-restriction fragment length polymorphism was used to genotype the GSTP1 and GSTM1, and GSTT1 polymorphisms. We found that the IIe/Val and Val/Val genotypes of GSTP1 showed more CR+PR to chemotherapy in advanced NSCLC when compared with IIe/IIe genotype, and the Ors (95% CI) were 0.37 (0.18-0.71) and 0.15 (0.07-0.38). The IIe/Val and Val/Val genotypes of GSTP1 were associated with longer overall survival of advanced NSCLC when compared with the IIe/IIe genotype (For IIe/Val vs IIe/IIe, 37.63 ± 2.01 months vs 30.25 ± 2.06 months; for Val/Val vs IIe/IIe, 39.84 ± 3.36 months vs 30.25 ± 2.06 months). In the Cox proportional hazards model, the IIe/Val and Val/Val genotypes significantly decreased risk of death from all causes in patients with advanced NSCLC, and the HRs (95% CIs) were 0.51 (0.28-0.94) and 0.35 (0.16-0.78), respectively. We found that the GSTP1 polymorphisms might affect the clinical outcome of patients with advanced NSCLC, and our results could help us to facilitate therapeutic decision for individualized therapy.

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