A Multicenter Trial Defining a Serum Protein Signature Associated with Pancreatic Ductal Adenocarcinoma

A. Gerdtsson, N. Malats, Anna Säll, F. Real, M. Porta, Petter Skoog, H. Persson, C. Wingren, C. Borrebaeck
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引用次数: 28

Abstract

Background. Pancreatic ductal adenocarcinoma (PDAC) is an aggressive disease with rapid tumor progression and poor prognosis. This study was motivated by the lack of sensitive and specific PDAC biomarkers and aimed to identify a diagnostic, serum protein signature for PDAC. Methods. To mimic a real life test situation, a multicenter trial comprising a serum sample cohort, including 338 patients with either PDAC or other pancreatic diseases (OPD) and controls with nonpancreatic conditions (NPC), was analyzed on 293-plex recombinant antibody microarrays targeting immunoregulatory and cancer-associated antigens. Results. Serum samples collected from different hospitals were analyzed and showed that (i) sampling from five different hospitals could not be identified as a preanalytical variable and (ii) a multiplexed biomarker signature could be identified, utilizing up to 10 serum markers that could discriminate PDAC from controls, with sensitivities and specificities in the 91–100% range. The first protein profiles associated with the location of the primary tumor in the pancreas could also be identified. Conclusions. The results demonstrate that robust enough serum signatures could be identified in a multicenter trial, potentially contributing to the development of a multiplexed biomarker immunoassay for improved PDAC diagnosis.
一项确定与胰腺导管腺癌相关的血清蛋白特征的多中心试验
背景。胰腺导管腺癌(PDAC)是一种侵袭性疾病,肿瘤进展迅速,预后差。这项研究的动机是缺乏敏感和特异性的PDAC生物标志物,旨在确定PDAC的诊断性血清蛋白特征。方法。为了模拟现实生活中的测试情况,一项包括血清样本队列的多中心试验,包括338例PDAC或其他胰腺疾病(OPD)患者和对照组非胰腺疾病(NPC)患者,采用293-plex重组抗体微阵列对免疫调节和癌症相关抗原进行分析。结果。对从不同医院收集的血清样本进行了分析,结果表明:(i)不能将来自五家不同医院的样本确定为分析前变量;(ii)可以利用多达10种可将PDAC与对照组区分开来的血清标记物,识别出多重生物标记物特征,其灵敏度和特异性在91-100%范围内。与胰腺原发肿瘤位置相关的第一个蛋白质谱也可以被确定。结论。结果表明,在多中心试验中可以识别出足够强大的血清特征,这可能有助于开发用于改善PDAC诊断的多重生物标志物免疫测定法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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