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CA19-9 和载脂蛋白 A2 异构体作为胰腺癌的检测标志物:一项前瞻性评估。

CA19-9 and apolipoprotein-A2 isoforms as detection markers for pancreatic cancer: a prospective evaluation.

机构信息

Department of Biomarker for Early Detection of Cancer, National Cancer Center Research Institute, Tokyo, Japan.

Japan Agency for Medical Research and Development (AMED) CREST, Tokyo, Japan.

出版信息

Int J Cancer. 2019 Apr 15;144(8):1877-1887. doi: 10.1002/ijc.31900. Epub 2018 Dec 4.

Abstract

Recently, we identified unique processing patterns of apolipoprotein A2 (ApoA2) in patients with pancreatic cancer. Our study provides a first prospective evaluation of an ApoA2 isoform ("ApoA2-ATQ/AT"), alone and in combination with carbohydrate antigen 19-9 (CA19-9), as an early detection biomarker for pancreatic cancer. We performed ELISA measurements of CA19-9 and ApoA2-ATQ/AT in 156 patients with pancreatic cancer and 217 matched controls within the European EPIC cohort, using plasma samples collected up to 60 months prior to diagnosis. The detection discrimination statistics were calculated for risk scores by strata of lag-time. For CA19-9, in univariate marker analyses, C-statistics to distinguish future pancreatic cancer patients from cancer-free individuals were 0.80 for plasma taken ≤6 months before diagnosis, and 0.71 for >6-18 months; for ApoA2-ATQ/AT, C-statistics were 0.62, and 0.65, respectively. Joint models based on ApoA2-ATQ/AT plus CA19-9 significantly improved discrimination within >6-18 months (C = 0.74 vs. 0.71 for CA19-9 alone, p = 0.022) and ≤ 18 months (C = 0.75 vs. 0.74, p = 0.022). At 98% specificity, and for lag times of ≤6, >6-18 or ≤ 18 months, sensitivities were 57%, 36% and 43% for CA19-9 combined with ApoA2-ATQ/AT, respectively, vs. 50%, 29% and 36% for CA19-9 alone. Compared to CA19-9 alone, the combination of CA19-9 and ApoA2-ATQ/AT may improve detection of pancreatic cancer up to 18 months prior to diagnosis under usual care, and may provide a useful first measure for pancreatic cancer detection prior to imaging.

摘要

最近,我们在胰腺癌患者中鉴定了载脂蛋白 A2(ApoA2)的独特处理模式。我们的研究首次前瞻性评估了载脂蛋白 A2 同工型(“ApoA2-ATQ/AT”)作为一种单独的早期检测生物标志物,以及与肿瘤相关抗原 19-9(CA19-9)联合使用,用于胰腺癌的早期检测。我们在欧洲 EPIC 队列中对 156 名胰腺癌患者和 217 名匹配对照者进行了 ELISA 测量,使用的是在诊断前长达 60 个月采集的血浆样本。通过滞后时间分层计算风险评分的检测判别统计数据。对于 CA19-9,在单变量标志物分析中,区分未来胰腺癌患者和无癌症个体的 C 统计量为诊断前≤6 个月时采集的血浆为 0.80,诊断前>6-18 个月时为 0.71;对于 ApoA2-ATQ/AT,C 统计量分别为 0.62 和 0.65。基于 ApoA2-ATQ/AT 加 CA19-9 的联合模型在>6-18 个月(CA19-9 单独为 0.74,p = 0.022)和≤18 个月(CA19-9 单独为 0.75,p = 0.022)时显著提高了判别能力。在特异性为 98%的情况下,对于滞后时间≤6、>6-18 或≤18 个月,CA19-9 联合 ApoA2-ATQ/AT 的敏感性分别为 57%、36%和 43%,而 CA19-9 单独为 50%、29%和 36%。与 CA19-9 单独相比,CA19-9 与 ApoA2-ATQ/AT 的联合应用可能会提高在常规护理下 18 个月前诊断胰腺癌的检测率,并且可能为在成像之前进行胰腺癌检测提供有用的首个指标。

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