Attallah A M, El-Far M, Ibrahim A R, El-Desouky M A, Omran M M, Elbendary M S, Attallah K A, Qura E R, Abdallah S O
a Research & Development Department , Biotechnology Research Center , New Damietta , Egypt.
b Chemistry Department, Faculty of Science , Mansoura University , Mansoura , Egypt.
Br J Biomed Sci. 2018 Jul;75(3):122-127. doi: 10.1080/09674845.2018.1456309. Epub 2018 May 8.
Although established markers such as CEA and CA19-9 are important for diagnosing early stages of colon cancer, they are not ideal. Developing promising markers include cytokeratin 1 (CK1) and mucin-1 (MUC1), but the combined value of each of these markers is unclear. We therefore evaluated the value of a combined laboratory-based score of these four markers in the diagnosis of colon cancer.
Two hundred patients who had undergone colonoscopic examination (150 colon cancer, 50 benign growths) were recruited. The study was controlled by 35 healthy subjects. CEA, CA19-9, CK1 and MUC1 were measured by ELISA and evaluated for cancer diagnosis using area under the receiver operating characteristic curve (AUC).
Serum levels of all four markers were increased in the order colon cancer > benign disease > healthy controls (p < 0.001). In multivariate analysis, CA19.9 (p = 0.025), CK1 (p < 0.001) and MUC1 (p = 0.009) were significant independent predictors of colon cancer. A score that gave the greatest power of discrimination for colon cancer was defined as 1.06 + [0.001 × CA19.9 result] + [0.003 × CEA result] + [0.03 × CK1 result] + [0.05 × MUC1 result]. The colon score provided superior discrimination, AUC, and sensitivity and specificity for colon cancer versus benign growth than each of the individual markers. Similarly, the colon score provided superior AUC, and sensitivity and specificity that each individual marker for tumour stage, lymph node invasion and distant organ metastases than each individual marker.
A colon score derived from serum CEA, CA19-9, CK1 and MUC1 is a potential valuable non-invasive index that could be used for detection and screening early stage colon cancer patients.
尽管癌胚抗原(CEA)和糖类抗原19-9(CA19-9)等既定标志物对结肠癌早期诊断很重要,但并不理想。有前景的标志物包括细胞角蛋白1(CK1)和粘蛋白1(MUC1),但这些标志物各自的联合价值尚不清楚。因此,我们评估了这四种标志物基于实验室的联合评分在结肠癌诊断中的价值。
招募了200例接受结肠镜检查的患者(150例结肠癌患者,50例良性肿瘤患者)。该研究以35名健康受试者作为对照。通过酶联免疫吸附测定(ELISA)法检测CEA、CA19-9、CK1和MUC1,并使用受试者操作特征曲线下面积(AUC)评估其对癌症的诊断价值。
所有四种标志物的血清水平按照结肠癌>良性疾病>健康对照的顺序升高(p<0.001)。在多变量分析中,CA19.9(p = 0.025)、CK1(p<0.001)和MUC1(p = 0.009)是结肠癌的显著独立预测因子。对结肠癌具有最大鉴别能力的评分定义为1.06 + [0.001×CA19.9结果] + [0.003×CEA结果] + [0.03×CK1结果] + [0.05×MUC1结果]。与单个标志物相比,结肠评分在鉴别结肠癌与良性肿瘤方面具有更高的鉴别能力、AUC、敏感性和特异性。同样,与单个标志物相比,结肠评分在肿瘤分期、淋巴结侵犯和远处器官转移方面具有更高的AUC、敏感性和特异性。
源自血清CEA、CA19-9、CK1和MUC1的结肠评分是一种潜在的有价值的非侵入性指标,可用于检测和筛查早期结肠癌患者。