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谷胱甘肽 S-转移酶 P1 和 XRCC1 的遗传多态性:预测晚期非小细胞肺癌(NSCLC)患者铂类化疗的临床疗效。

Genetic polymorphisms of GSTP1 and XRCC1: prediction of clinical outcome of platinum-based chemotherapy in advanced non-small cell lung cancer (NSCLC) patients.

机构信息

Department of Oncology, The Affiliated Hospital of Medical College, Qing Dao University, Qingdao, Shandong Province, China.

出版信息

Swiss Med Wkly. 2011 Oct 19;141:w13275. doi: 10.4414/smw.2011.13275. eCollection 2011.

Abstract

PRINCIPLES

Platinum agents cause DNA cross-linking and oxidative damage. Genetic polymorphisms of GSTP1 and XRCC1 involved in glutathione metabolic and DNA repair pathways may explain inter individual differences in chemosensitivity and clinical outcome in NSCLC patients treated with platinum-based regimens.

METHODS

We used DNA sequencing methods to evaluate genetic polymorphisms of the GSTP1A313G and XRCC1G28152A in 111 patients with stage IV NSCLC treated with platinum-based chemotherapy. Clinical response was evaluated according to RECIST criteria after 2-3 cycles of chemotherapy and time to progression (TTP) was calculated from the time of initial treatment to disease progression.

RESULTS

GSTP1A313G and XRCC1G28152A polymorphisms, both alone and in combination, were significantly associated with response to treatment and clinical outcome (p <0.05) in NSCLC patients treated with platinum-based chemotherapy. These polymorphisms independently predicted clinical outcome even after taking into account age, gender, tumour histology, tumour differentiation and chemotherapy regimens.

CONCLUSION

Genetic polymorphisms of GSTP1 and XRCC1 may be important predictive factors in platinum-treated patients with advanced NSCLC. Assessment of genetic variations of GSTP1 and XRCC1 could facilitate therapeutic decisions for individualised therapy in advanced NSCLC.

摘要

原则

铂类药物会导致 DNA 交联和氧化损伤。参与谷胱甘肽代谢和 DNA 修复途径的 GSTP1 和 XRCC1 的遗传多态性,可能解释了接受铂类方案治疗的 NSCLC 患者的化疗敏感性和临床结局的个体差异。

方法

我们使用 DNA 测序方法评估了 111 例接受铂类化疗的 IV 期 NSCLC 患者 GSTP1A313G 和 XRCC1G28152A 的遗传多态性。根据化疗 2-3 周期后的 RECIST 标准评估临床反应,从初始治疗到疾病进展的时间计算无进展生存期(TTP)。

结果

GSTP1A313G 和 XRCC1G28152A 多态性,无论是单独存在还是联合存在,与接受铂类化疗的 NSCLC 患者的治疗反应和临床结局均显著相关(p<0.05)。这些多态性独立预测了临床结局,即使考虑了年龄、性别、肿瘤组织学、肿瘤分化和化疗方案。

结论

GSTP1 和 XRCC1 的遗传多态性可能是晚期 NSCLC 铂类治疗患者的重要预测因素。评估 GSTP1 和 XRCC1 的遗传变异可能有助于为晚期 NSCLC 患者的个体化治疗做出治疗决策。

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