首页> 外文会议>American Society for Mass Spectrometry Conference on Mass Spectrometry and Allied Topics >Digital pathology: Discovering and verifying Barretts' disease progression markers in tissue samples using LCM-coupled SRM assays.
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Digital pathology: Discovering and verifying Barretts' disease progression markers in tissue samples using LCM-coupled SRM assays.

机译:数字病理学:使用LCM偶联的SRM测定发现和验证BARTETS'疾病进展标志物中的组织样品。

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The incidence of esophageal adenocarcinoma (EAC) arising from Barrett's esophagus (BE) has increased by 350percent since 1970, and at the time of presentation, 50percent of patients will have advanced disease with virtually no chance for cure. The prognosis for EAC arising from BE is poor with an overall 5-year survival rate less than 15percent, with no verified progression markers. So there is clearly a need to define those patients at highest risk for cancer development beyond the histologic identification of dysplasia within a BE field. Currently, risk for esophageal cancer is determined by the histologic appearance of BE, however there is a large degree of intra- and inter-observer variability among pathologists.
机译:自1970年以来,巴雷特食管引起的食管腺癌(EAC)的发病率增加了350%,并且在介绍时,50%的患者将具有晚期治疗方法。 EAC的预后较差,总体5年生存率小于15年,没有经过验证的进展标记。因此,显然需要将这些患者定义最高风险的癌症发展,超出了域内发育不良的组织学鉴定。目前,食管癌的风险由组织学外观决定,然而,病理学家之间存在很大程度的互相间变异性。

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