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首页> 外文期刊>Oncologie. >Toward a personalized treatment of colorectal cancer: Prognostic and predictive factors [Vers un traitement personnalisé du cancer colorectal: Facteurs pronostiques et prédictifs]
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Toward a personalized treatment of colorectal cancer: Prognostic and predictive factors [Vers un traitement personnalisé du cancer colorectal: Facteurs pronostiques et prédictifs]

机译:走向大肠癌的个性化治疗:预后和预测因素[走向大肠癌的个性化治疗:预后和预测因素]

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摘要

Colorectal cancer (CRC) remains a major public health problem despite the advent of several conventional chemotherapies and targeted therapies. The identification of prognostic factors, and also factors that can predict response to different treatments and their toxicity, has become amajor issue in order to optimize and personalize treatment of CRC patients. Although few molecular factors are validated in the field of CRC prognosis where the TNM classification is the main parameter used in clinical practice, the fact is not true for molecular predictive factors. Several of them are now validated for predicting response to certain treatments (KRAS mutations and anti-EGFR antibodies) and their toxicity (dihydropyrimidine déshydrogenase [DPD] for 5-fluorouracil [5-FU], UDP-glucuronosyltransferase 1A1 [UGT 1A1] polymorphism for irinotecan) and open up the way of personalized treatment of CRC.
机译:尽管出现了几种常规化学疗法和靶向疗法,但结直肠癌(CRC)仍然是主要的公共卫生问题。为了优化和个性化CRC患者的治疗,识别预后因素以及可以预测对不同治疗方法及其毒性的反应的因素已经成为主要问题。尽管在TNM分类是临床实践中主要参数的CRC预后领域中,很少有分子因素得到验证,但对于分子预测因素而言,事实并非如此。现在已经验证了其中的几种药物,可预测对某些治疗(KRAS突变和抗EGFR抗体)的反应及其毒性(5-氢尿嘧啶[5-FU]的二氢嘧啶脱氢酶[DPD],UDP-葡萄糖醛酸转移酶1A1 [UGT 1A1]多态性) irinotecan),开辟了CRC个性化治疗的途径。

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