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Should mismatch repair status be determined in all stage II and III colon cancer patients?

机译:是否应在所有II期和III期结肠癌患者中确定错配修复状态?

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Microsatellite instability constitutes an important oncogenic molecular pathway in colon cancer (12-15%). Microsatellite instability is a molecular marker of deficient DNA mismatch repair (MMR), which occurs from somatic hypermethylation of the MLH1 promoter or less frequently as a result of germline mutations in MMR genes. The excellent prognosis of patients with stage II deficient MMR colon cancer today, makes this information mandatory in order to decide or not on adjuvant chemotherapy. MMR deficiency may also predict tumor chemoresistance to 5-fluorouracil adjuvant treatment. However, when looking at very recent data on 5-fluorouracil plus oxaliplatin-based adjuvant regimens, it seems that the benefit of this adjuvant therapy is similar between deficient and proficient MMR patients.
机译:微卫星不稳定性是结肠癌的重要致癌分子途径(12-15%)。微卫星不稳定性是DNA错配修复(MMR)不足的分子标记,它是由MLH1启动子的体细胞超甲基化引起的,或者是由于MMR基因中的种系突变而引起的。今天,II期缺陷MMR结肠癌患者的良好预后使该信息成为强制性信息,以便决定是否进行辅助化疗。 MMR缺乏症也可能预测肿瘤对5-氟尿嘧啶辅助治疗的耐药性。但是,当查看基于5-氟尿嘧啶加奥沙利铂为基础的辅助治疗方案的最新数据时,似乎该MMM患者与辅助治疗的获益相似。

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