O'Brien Darragh P, Sandanayake Neomal S, Jenkinson Claire, Gentry-Maharaj Aleksandra, Apostolidou Sophia, Fourkala Evangelia-Ourania, Camuzeaux Stephane, Blyuss Oleg, Gunu Richard, Dawnay Anne, Zaikin Alexey, Smith Ross C, Jacobs Ian J, Menon Usha, Costello Eithne, Pereira Stephen P, Timms John F
Women's Cancer, Institute for Women's Health, University College London, London, United Kingdom.
Institute for Liver and Digestive Health, University College London, Royal Free Hospital, London, United Kingdom. Kolling Institute, University of Sydney, Royal North Shore Hospital, New South Wales, Australia.
Clin Cancer Res. 2015 Feb 1;21(3):622-31. doi: 10.1158/1078-0432.CCR-14-0365. Epub 2014 Jun 17.
Biomarkers for the early detection of pancreatic cancer are urgently needed. The primary objective of this study was to evaluate whether increased levels of serum CA19-9, CA125, CEACAM1, and REG3A are present before clinical presentation of pancreatic cancer and to assess the performance of combined markers for early detection and prognosis.
This nested case-control study within the UKCTOCS included 118 single and 143 serial serum samples from 154 postmenopausal women who were subsequently diagnosed with pancreatic cancer and 304 matched noncancer controls. Samples were split randomly into independent training and test sets. CA19-9, CA125, CEACAM1, and REG3A were measured using ELISA and/or CLIA. Performance of markers to detect cancers at different times before diagnosis and for prognosis was evaluated.
At 95% specificity, CA19-9 (>37 U/mL) had a sensitivity of 68% up to 1 year, and 53% up to 2 years before diagnosis. Combining CA19-9 and CA125 improved sensitivity as CA125 was elevated (>30 U/mL) in approximately 20% of CA19-9-negative cases. CEACAM1 and REG3A were late markers adding little in combined models. Average lead times of 20 to 23 months were estimated for test-positive cases. Prediagnostic levels of CA19-9 and CA125 were associated with poor overall survival (HR, 2.69 and 3.15, respectively).
CA19-9 and CA125 have encouraging sensitivity for detecting preclinical pancreatic cancer, and both markers can be used as prognostic tools. This work challenges the prevailing view that CA19-9 is upregulated late in the course of pancreatic cancer development.
迫切需要用于早期检测胰腺癌的生物标志物。本研究的主要目的是评估血清CA19-9、CA125、癌胚抗原相关细胞黏附分子1(CEACAM1)和再生胰岛衍生蛋白3α(REG3A)水平升高是否出现在胰腺癌临床表现之前,并评估联合标志物用于早期检测和预后的性能。
在英国癌症研究(UKCTOCS)中的这项巢式病例对照研究纳入了154名随后被诊断为胰腺癌的绝经后女性的118份单次血清样本和143份系列血清样本,以及304名匹配的非癌症对照。样本被随机分为独立的训练集和测试集。使用酶联免疫吸附测定(ELISA)和/或化学发光免疫分析(CLIA)检测CA19-9、CA125、CEACAM1和REG3A。评估标志物在诊断前不同时间检测癌症以及用于预后的性能。
在95%的特异性下,CA19-9(>37 U/mL)在诊断前1年的灵敏度为68%,在诊断前2年的灵敏度为53%。联合CA19-9和CA125可提高灵敏度,因为在大约20%的CA19-9阴性病例中CA125升高(>30 U/mL)。CEACAM1和REG3A是晚期标志物,在联合模型中作用不大。估计检测呈阳性的病例的平均提前期为20至23个月。CA19-9和CA125的诊断前水平与总体生存率差相关(风险比分别为2.69和3.15)。
CA19-9和CA125在检测临床前胰腺癌方面具有令人鼓舞的灵敏度,并且这两种标志物均可用作预后工具。这项工作挑战了CA19-9在胰腺癌发展过程后期上调的主流观点。