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CA19-9 的时间轨迹作为胰腺癌早期检测的锚定标志物。

Lead-Time Trajectory of CA19-9 as an Anchor Marker for Pancreatic Cancer Early Detection.

机构信息

Department of Clinical Cancer Prevention, The University of Texas M. D. Anderson Cancer Center, Houston, Texas.

Department of Surgery, Indiana University School of Medicine, Indianapolis, Indiana.

出版信息

Gastroenterology. 2021 Mar;160(4):1373-1383.e6. doi: 10.1053/j.gastro.2020.11.052. Epub 2020 Dec 14.

Abstract

BACKGROUND & AIMS: There is substantial interest in liquid biopsy approaches for cancer early detection among subjects at risk, using multi-marker panels. CA19-9 is an established circulating biomarker for pancreatic cancer; however, its relevance for pancreatic cancer early detection or for monitoring subjects at risk has not been established.

METHODS

CA19-9 levels were assessed in blinded sera from 175 subjects collected up to 5 years before diagnosis of pancreatic cancer and from 875 matched controls from the Prostate, Lung, Colorectal and Ovarian (PLCO) Cancer Screening Trial. For comparison of performance, CA19-9 was assayed in blinded independent sets of samples collected at diagnosis from 129 subjects with resectable pancreatic cancer and 275 controls (100 healthy subjects; 50 with chronic pancreatitis; and 125 with noncancerous pancreatic cysts). The complementary value of 2 additional protein markers, TIMP1 and LRG1, was determined.

RESULTS

In the PLCO cohort, levels of CA19-9 increased exponentially starting at 2 years before diagnosis with sensitivities reaching 60% at 99% specificity within 0 to 6 months before diagnosis for all cases and 50% at 99% specificity for cases diagnosed with early-stage disease. Performance was comparable for distinguishing newly diagnosed cases with resectable pancreatic cancer from healthy controls (64% sensitivity at 99% specificity). Comparison of resectable pancreatic cancer cases to subjects with chronic pancreatitis yielded 46% sensitivity at 99% specificity and for subjects with noncancerous cysts, 30% sensitivity at 99% specificity. For prediagnostic cases below cutoff value for CA19-9, the combination with LRG1 and TIMP1 yielded an increment of 13.2% in sensitivity at 99% specificity (P = .031) in identifying cases diagnosed within 1 year of blood collection.

CONCLUSION

CA19-9 can serve as an anchor marker for pancreatic cancer early detection applications.

摘要

背景与目的

在有风险的受试者中,使用多标志物面板,液体活检方法在癌症早期检测方面引起了广泛关注。CA19-9 是一种已确立的胰腺癌循环生物标志物;然而,其在胰腺癌早期检测或监测风险受试者方面的相关性尚未确定。

方法

在前列腺癌、肺癌、结直肠癌和卵巢癌(PLCO)癌症筛查试验中,对 175 名受试者在诊断前 5 年内采集的盲血清中的 CA19-9 水平进行了评估,并对 875 名匹配对照进行了评估。为了比较性能,在可切除胰腺癌和 275 名对照(100 名健康受试者;50 名慢性胰腺炎患者;125 名非癌性胰腺囊肿患者)的诊断时采集的盲独立样本中检测了 CA19-9。还确定了另外两种蛋白质标志物 TIMP1 和 LRG1 的互补价值。

结果

在 PLCO 队列中,CA19-9 水平呈指数增长,从诊断前 2 年开始,所有病例在诊断前 0 至 6 个月内达到 99%特异性时的灵敏度达到 60%,而早期疾病诊断的病例灵敏度为 50%。对于从健康对照中区分新诊断的可切除胰腺癌病例,性能相当(99%特异性时 64%的灵敏度)。将可切除的胰腺癌病例与慢性胰腺炎患者进行比较,特异性为 99%时灵敏度为 46%,与非癌性囊肿患者相比,特异性为 99%时灵敏度为 30%。对于 CA19-9 截断值以下的预测病例,LRG1 和 TIMP1 的组合在以 99%特异性识别采血后 1 年内诊断的病例时,灵敏度提高了 13.2%(P=0.031)。

结论

CA19-9 可作为胰腺癌早期检测应用的锚定标志物。

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