用户名: 密码: 验证码:
血清前列腺特异性抗原联合血清肿瘤相关物质在早期前列腺癌诊断中的应用分析
详细信息    查看全文 | 推荐本文 |
  • 英文篇名:Application of serum prostate specific antigen combined with serum tumor associated material in the early diagnosis of prostate cancer
  • 作者:赵琪 ; 刘秉乾 ; 何长海 ; 李保安 ; 王志 ; 王雪峰
  • 英文作者:ZHAO Qi;LIU Bingqian;HE Changhai;LI Baoan;WANG Zhi;WANG Xuefeng;Department of Urologic Surgery,Nanyang First People's Hospital;Department of Urologic Surgery,the First Affiliated Hospital of Zhengzhou University;
  • 关键词:血清前列腺特异性抗原 ; 血清肿瘤相关物质 ; 前列腺癌 ; 诊断价值
  • 英文关键词:serum prostate specific antigen;;serum tumor associated material;;prostate cancer;;diagnostic value
  • 中文刊名:AZJZ
  • 英文刊名:Oncology Progress
  • 机构:南阳市第一人民医院泌尿外科;郑州大学第一附属医院泌尿外科;
  • 出版日期:2019-01-10
  • 出版单位:癌症进展
  • 年:2019
  • 期:v.17
  • 语种:中文;
  • 页:AZJZ201901012
  • 页数:3
  • CN:01
  • ISSN:11-4971/R
  • 分类号:55-57
摘要
目的分析血清前列腺特异性抗原(PSA)联合血清肿瘤相关物质(TAM)在早期诊断前列腺癌中的应用价值。方法选择128例前列腺癌患者为病例组,另选择128例前列腺良性病变者为对照组,检测所有患者PSA及TAM值,分析PSA联合TAM在早期诊断前列腺癌中的应用价值。结果以PSA≥4.08 ng/ml为诊断前列腺癌的临界值,PSA诊断前列腺癌的准确度、特异度以及灵敏度分别为82.8%、76.1%和88.6%,受试者工作特征(ROC)曲线下面积为0.873。以TAM≥98.36 U/ml为诊断前列腺癌的临界值,TAM诊断前列腺癌的准确度、特异度以及灵敏度分别为77.3%、78.7%和74.5%,ROC曲线下面积为0.832。实施双指标联合检测,特异度为96.6%,高于单一指标诊断特异度。病例组患者TAM和PSA水平均高于对照组,差异均有统计学意义(P﹤0.05)。结论在进行筛查以及早期诊断前列腺癌中,采用PSA及TAM联合检测法,可提升诊断特异度,令检查结果更为精准,值得进一步在临床中推广应用。
        Objective To analyze the value of serum prostate specific antigen(PSA) combined with serum tumor associated material(TAM) in the early diagnosis of prostate cancer. Method 128 patients with prostate cancer were included as case group, while another 128 with benign prostate lesions were recruited as control, of which the PSA and TAM levels were detected to determine the diagnostic value of both measures in the early diagnosis of prostate cancer. Result With PSA≥4.08 ng/ml as the critical value for confirming prostate cancer, the accuracy, specificity and sensitivity of PSA in the diagnosis of prostate cancer were 82.8%, 76.1% and 88.6%, respectively, and the area under the curve of receiver operating characteristic(ROC) curve was 0.873. With TAM ≥98.36 U/ml as the critical value instead, the accuracy, specificity and sensitivity of TAM in the diagnosis of prostate cancer were 77.3%, 78.7% and 74.5%, respectively, with AUC of ROC being 0.832. When combined, the coupled detection indicated a specificity as high as 96.6%, which was higher than that of each measure used alone. The levels of TAM and PSA in the case group were significantly higher than those in control group, demonstrating statistically significant difference(P<0.05). Conclusion In the screening and early diagnosis of prostate cancer, the combined detection of PSA and TAM can improve the diagnostic specificity and accuracy.
引文
[1]闫存玲,李志艳,何群,等.血清前列腺特异性抗原同源异构体2在前列腺癌诊断中的应用价值[J].中华检验医学杂志, 2015, 38(12):813-817.
    [2]翟玉普,闫成全.多种肿瘤标志物联合前列腺特异性抗原检测在前列腺癌诊断中的价值[J].中国性科学, 2016, 25(8):7-10.
    [3]郭小鹏,成俊,王鹏.血清前列腺特异抗原、直肠指检联合磁共振波谱成像对前列腺癌的诊断价值[J].中国实验诊断学, 2016, 20(3):381-384.
    [4]刘妍,徐勇,刘冉录,等.血清PSA、PSAD检测在前列腺癌骨转移诊断中的价值[J].山东医药, 2015, 55(5):1-3; 6.
    [5]李浩,王晓东,郜乐,等.血清各项前列腺特异性抗原数值联合磁共振弥散加权中表观扩散系数及波谱成像对前列腺特异性抗原灰区前列腺癌的诊断应用[J].中国医师进修杂志, 2016, 39(3):249-253.
    [6]庞宽,周泽光,刘成倍,等.对血清前列腺特异性抗原<10.0μg/L者行经会阴饱和前列腺穿刺活检诊断前列腺癌的价值[J].中国性科学, 2015, 24(4):47-50.
    [7]杨宗珂,王德林,杨研,等.前列腺特异性抗原及其相关指标在前列腺癌鉴别诊断中的应用价值[J].中国医学装备,2015, 12(12):31-35.
    [8]谢冲,黄其伟,王国民,等.多种肿瘤标志物联合前列腺特异性抗原检测在前列腺癌诊断中的价值[J].中华泌尿外科杂志, 2015, 36(3):204-208.
    [9]吴义启,刘修恒.前列腺特异性抗原前体2型及其百分比、前列腺健康指数对前列腺癌的诊断价值[J].现代泌尿外科杂志, 2015, 20(7):525-527.
    [10] Xue D, Zhou CX, Shi YB, et al. MD-miniRNA could be a more accurate biomarker for prostate cancer screening compared with serum prostate-specific antigen level[J].Tumour Biol, 2015, 36(5):3541-3547.
    [11] Nnabugwu II, Ugwumba FO, Enivwenae OA, et al. Serum total prostate-specific antigen values in men with symptomatic prostate enlargement in Nigeria:role in clinical decision-making[J]. Clin Interv Aging, 2015, 10:89-93.
    [12]周俊,宋建达,夏术阶.血清肿瘤相关物质群和前列腺特异性抗原诊断前列腺癌的比较[J].上海医学, 2006, 29(6):356-358.

© 2004-2018 中国地质图书馆版权所有 京ICP备05064691号 京公网安备11010802017129号

地址:北京市海淀区学院路29号 邮编:100083

电话:办公室:(+86 10)66554848;文献借阅、咨询服务、科技查新:66554700