首页> 外文OA文献 >MTHFR-1298 A>C (rs1801131) is a predictor of survival in two cohorts of stage II/III colorectal cancer patients treated with adjuvant fluoropyrimidine chemotherapy with or without oxaliplatin
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MTHFR-1298 A>C (rs1801131) is a predictor of survival in two cohorts of stage II/III colorectal cancer patients treated with adjuvant fluoropyrimidine chemotherapy with or without oxaliplatin

机译:MTHFR-1298 A> C(rs1801131)是两个接受氟尿嘧啶辅助化疗和/或奥沙利铂辅助治疗的II / III期结直肠癌患者队列的生存预测指标

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摘要

Adjuvant treatment based on fluoropyrimidines (FL) improves the prognosis of stage II/III colorectal cancer (CRC). Validated predictive/prognostic biomarkers would spare therapy-related morbidity in patients with a good prognosis. We compared the impact of a set of 22 FL-related polymorphisms with the prognosis of two cohorts of CRC patients treated with adjuvant FL with or without OXA, including a total of 262 cases. 5,10-Methylentetrahydrofolate reductase (MTHFR) MTHFR-1298 A>C (rs1801131) polymorphism had a concordant effect: MTHFR-rs1801131-1298CC genotype carriers had a worse disease free survival (DFS) in both the cohorts. In the pooled population MTHFR-rs1801131-1298CC carriers had also a worse overall survival. We computed a clinical score related to DFS including MTHFR-rs1801131, tumor stage, sex and tumor location, where rs1801131 is the most detrimental factor (hazard ratio=5.3, 95% confidence interval=2.2-12.9; P-value=0.0006). MTHFR-rs1801131 is a prognostic factor that could be used as an additional criteria for the choice of the proper adjuvant regimen in stage II/III colorectal cancer patients.
机译:基于氟嘧啶(FL)的辅助治疗可改善II / III期大肠癌(CRC)的预后。经过验证的预测性/预后性生物标志物可以使预后良好的患者免于与治疗相关的发病率。我们比较了一组22种FL相关基因多态性的影响与两个接受辅助FL或无OXA辅助治疗的CRC患者队列的预后,共计262例。 5,10-亚甲基四氢叶酸还原酶(MTHFR)MTHFR-1298 A> C(rs1801131)多态性具有协调一致的作用:MTHFR-rs1801131-1298CC基因型携带者在两个队列中均具有较差的无病生存期(DFS)。在合并人群中,MTHFR-rs1801131-1298CC携带者的整体生存率也较差。我们计算了与DFS相关的临床评分,包括MTHFR-rs1801131,肿瘤分期,性别和肿瘤位置,其中rs1801131是最有害的因素(危险比= 5.3,95%置信区间= 2.2-12.9; P值= 0.0006)。 MTHFR-rs1801131是一种预后因素,可以作为选择II / III期大肠癌患者合适佐剂方案的附加标准。

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