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.
Gastroenterology. 2021 Mar;160(4):1373-1383.e6. doi: 10.1053/j.gastro.2020.11.052. Epub 2020 Dec 14.
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.
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.
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.
CA19-9 can serve as an anchor marker for pancreatic cancer early detection applications.
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。
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。
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)。
CA19-9 可作为胰腺癌早期检测应用的锚定标志物。