Diagnostic value of serum fibrin degradation complex DR-70 combined with conventional tumor biomarkers in colorectal cancer.

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Xiaoxia Wang, Wei Wei, Nanni Hua, Chunyan Li, Lili Yu
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引用次数: 0

Abstract

Objective: Most patients with colorectal cancer (CRC) show no early symptoms, and tumor markers have low sensitivity and specificity. We therefore investigated the ability of serum fibrin degradation complex DR-70 plus traditional tumor markers to diagnose CRC.

Methods: We retrospectively screened patients with CRC or non-malignant colorectal diseases, as well as healthy individuals, for inclusion in this study. The individuals' clinical characteristics were recorded, and serum samples were collected. Expression levels of DR-70 and conventional tumor markers were measured by enzyme-linked immunosorbent assay and electrochemiluminescence.

Results: DR-70 levels differed significantly among patients with CRC, patients with benign colorectal diseases, and healthy individuals. Receiver operating characteristic curve analysis identified DR-70 as a conventional tumor marker with the highest sensitivity and the second-highest specificity after carcinoembryonic antigen.

Conclusions: This study identified DR-70 as a reliable marker for the detection, differentiation, and progression of CRC, with good sensitivity and specificity. DR-70 measurement could greatly improve the efficacy of CRC diagnosis when used together with other tumor markers.

血清纤维蛋白降解复合物 DR-70 与传统肿瘤生物标志物相结合对结直肠癌的诊断价值。
目的:大多数结直肠癌(CRC)患者没有早期症状,而肿瘤标志物的敏感性和特异性较低。因此,我们研究了血清纤维蛋白降解复合物 DR-70 加上传统肿瘤标志物诊断 CRC 的能力:方法:我们对患有 CRC 或非恶性结直肠疾病的患者以及健康人进行了回顾性筛选。记录患者的临床特征并采集血清样本。通过酶联免疫吸附试验和电化学发光法测定 DR-70 和传统肿瘤标志物的表达水平:结果:DR-70的水平在CRC患者、良性结直肠疾病患者和健康人之间存在显著差异。接收者操作特征曲线分析确定 DR-70 是一种常规肿瘤标记物,其灵敏度最高,特异性仅次于癌胚抗原:本研究发现 DR-70 是检测、分化和评估 CRC 进展的可靠标志物,具有良好的灵敏度和特异性。如果与其他肿瘤标志物一起使用,DR-70 的测量可大大提高 CRC 诊断的有效性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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