Department of Medicine, University of Montreal, Montreal, QC, Canada; Division of Gastroenterology, Maisonneuve-Rosemont Hospital, Montreal, QC, Canada.
ATGen Canada Inc, Laval, QC, Canada.
Gastroenterology. 2017 Oct;153(4):980-987. doi: 10.1053/j.gastro.2017.06.009. Epub 2017 Jun 15.
BACKGROUND & AIMS: Low activity of natural killer (NK) cells has been associated with increased risk of cancer and has been reported in patients with colorectal cancer (CRC). Activity of NK cells can be measured in a small volume of whole blood by a commercially available test. We investigated whether this test could be used to identify patients with CRC, using findings from colonoscopy as a reference standard.
We performed an open-label, prospective, cross-sectional study of 872 high-risk subjects (more than 40 years old) screened for CRC by colonoscopy at a university hospital in Montreal, Canada from October 2014 through January 2016. Blood samples were collected on the day of colonoscopy, prior to the procedure. The test involves stimulation of whole blood with cytokine that induces NK cells to secrete interferon gamma (IFNG), which is quantified by an ELISA. Tissue samples were taken from lesions during the colonoscopy and analyzed histologically; subjects were classified as having no evidence of disease, adenomatous polyps of less than 10 mm, of 10 mm or more, or CRC. We used the non-parametric Mann-Whitney test to compare NK cell activity between subjects with no evidence of CRC and subjects found to have CRC. Receiver operating characteristic curve analysis was used to assess the ability of the test to identify individuals with CRC. The primary objective was to determine the difference in NK cell activity between subjects with vs without CRC. The secondary objective was the test performance, based on receiver operating characteristic analysis, and cut-off value that most accurately identified individuals with CRC.
We found a significant difference in NK cell activity between the 23 subjects with CRC (based on pathology analysis) and the 849 subjects without CRC: subjects found to have CRC by colonoscopy had a median level of 86.0 pg IFNG/mL (inter-quartile range, 43.3-151.0 pg IFNG/mL), whereas subjects without CRC had a median level of 298.1 pg IFNG/mL (inter-quartile range, 100.4-920.2 pg IFNG/mL) (P = .0002). The cut-off value that most accurately identified subjects with CRC was 181 pg/mL. The NK cell activity test identified subjects with CRC with 87.0% sensitivity, 60.8% specificity, a positive predictive value of 5.7%, and a negative predictive value of 99.4%. The odds ratio for detection of CRC in subjects with low NK cell activity vs subjects with higher NK cell activity was 10.3 (95% CI, 3.03-34.9).
Using colonoscopy as the reference standard, a test for NK cell activity in whole blood samples identified patients with CRC with 87.0% sensitivity and a negative predictive value of 99.4%. Subjects with low NK cell activity had a 10-fold higher risk of CRC compared with subjects with high NK cell activity. This test might be used in clinical practice to assess patients for risk of CRC. Clinicaltrials.gov number: NCT02291198.
自然杀伤 (NK) 细胞活性降低与癌症风险增加相关,并且在结直肠癌 (CRC) 患者中已有报道。NK 细胞的活性可以通过商业上可获得的测试在小体积的全血中进行测量。我们研究了这种测试是否可以用于识别 CRC 患者,以结肠镜检查结果作为参考标准。
我们对 2014 年 10 月至 2016 年 1 月在加拿大蒙特利尔的一家大学医院接受结肠镜检查筛查 CRC 的 872 名高危受试者(年龄超过 40 岁)进行了一项开放标签、前瞻性、横断面研究。在结肠镜检查当天采集血液样本,在检查前采集。该测试涉及用细胞因子刺激全血,诱导 NK 细胞分泌干扰素 γ (IFNG),通过 ELISA 定量。从结肠镜检查过程中的病变处采集组织样本并进行组织学分析;将受试者分为无 CRC 证据、腺瘤性息肉小于 10mm、10mm 或更大、或 CRC。我们使用非参数曼-惠特尼检验比较无 CRC 证据的受试者和发现 CRC 的受试者之间的 NK 细胞活性。使用接收者操作特征曲线分析评估该测试识别 CRC 个体的能力。主要目的是确定有和无 CRC 的受试者之间 NK 细胞活性的差异。次要目标是基于接收者操作特征分析的测试性能和最准确识别 CRC 个体的截断值。
我们发现,23 名经病理分析发现 CRC 的受试者与 849 名无 CRC 的受试者之间的 NK 细胞活性存在显著差异:通过结肠镜检查发现 CRC 的受试者的中位 IFNG 水平为 86.0pg/mL(四分位距,43.3-151.0pg/mL),而无 CRC 的受试者的中位 IFNG 水平为 298.1pg/mL(四分位距,100.4-920.2pg/mL)(P=0.0002)。最准确识别 CRC 受试者的截断值为 181pg/mL。NK 细胞活性测试对 CRC 受试者的灵敏度为 87.0%,特异性为 60.8%,阳性预测值为 5.7%,阴性预测值为 99.4%。NK 细胞活性低的受试者与 NK 细胞活性高的受试者相比,CRC 的检出率比值为 10.3(95%CI,3.03-34.9)。
以结肠镜检查为参考标准,对全血样本中 NK 细胞活性的检测可识别出 87.0%的 CRC 患者,阴性预测值为 99.4%。与 NK 细胞活性高的受试者相比,NK 细胞活性低的受试者 CRC 的风险高 10 倍。该检测方法可用于临床实践中评估患者的 CRC 风险。临床试验注册编号:NCT02291198。