首页> 美国卫生研究院文献>Journal of Experimental Clinical Cancer Research : CR >TNFRSF1B A1466G genotype is predictive of clinical efficacy after treatment with a definitive 5-fluorouracil/cisplatin-based chemoradiotherapy in Japanese patients with esophageal squamous cell carcinoma
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TNFRSF1B A1466G genotype is predictive of clinical efficacy after treatment with a definitive 5-fluorouracil/cisplatin-based chemoradiotherapy in Japanese patients with esophageal squamous cell carcinoma

机译:TNFRSF1B A1466G基因型可预测在日本食管鳞状细胞癌患者中应用基于5-氟尿嘧啶/顺铂的定性放化疗后的临床疗效

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摘要

BackgroundCurrently definitive 5-fluorouracil (5-FU)/cisplatin (CDDP) -based chemotherapy is recognized as one of the most promising treatments for esophageal cancer. A series of studies performed found genetic polymorphisms and the plasma concentration of 5-FU to be predictive of acute severe toxicities and clinical response. Genetic polymorphisms of tumor necrosis factor (TNF) -α and its surface receptors, TNFRSF1A and TNFRSF1B have been examined in terms of susceptibility to various cancers. In this study, genetic polymorphisms of TNFRSF1B gene were evaluated Japanese esophageal squamous cell carcinoma (ESCC) patients treated with the definitive 5-FU/CDDP-based chemoradiotherapy and their predictive values of prognosis or severe acute toxicities were assessed.
机译:背景技术目前,基于确定性的5-氟尿嘧啶(5-FU)/顺铂(CDDP)的化疗被认为是食道癌最有前途的治疗方法之一。进行的一系列研究发现,遗传多态性和5-FU的血浆浓度可预测急性严重毒性和临床反应。肿瘤坏死因子(TNF)-α及其表面受体TNFRSF1A和TNFRSF1B的遗传多态性已根据对各种癌症的敏感性进行了研究。在这项研究中,评估了TNFRSF1B基因的遗传多态性,对日本食管鳞状细胞癌(ESCC)患者进行了基于5-FU / CDDP的放化疗的确诊,并评估了其对预后或严重急性毒性的预测价值。

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