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肿瘤标记物联合检测对肿瘤高危人群筛查的临床意义
引用本文:邓伟伟,黄艳春,阿先古丽·阿不力孜. 肿瘤标记物联合检测对肿瘤高危人群筛查的临床意义[J]. 国际免疫学杂志, 2016, 0(1): 29-33. DOI: 10.3760/cma.j.issn.1673-4394.2016.01.006
作者姓名:邓伟伟  黄艳春  阿先古丽·阿不力孜
作者单位:新疆医科大学附属肿瘤医院检验科,乌鲁木齐市,830011
摘    要:目的 研究应用肿瘤标记物联合检测对恶性肿瘤高危人群筛查的临床价值.方法 选择血清肿瘤标记物组合对3 766例恶性肿瘤高危人员进行检测,对肿瘤标记(CA125、CEA、Cyfra21-1、CA19-9、AFP、NSE、CA72-4、SCC、CA153)升高人员进一步行颈胸部CT、腹盆部CT或内窥镜检查,女性进行妇科检查,未明确诊断者进行长期随访(大于6个月).结果 经过随访,共发现肿瘤患者69例,其中发现肿瘤标志物升高6个月内诊断为恶性肿瘤20例(62.5%),6个月至1年诊断5例(15.6%),1年至2年诊断4例(12.5%),2年至3年诊断2例(9.4%).COX分析显示肿瘤标志物升高的程度(RR=2.308,95% CI:2.517 ~2.475,P<0.001)、肿瘤标志物逐渐升高(RR=7.727,95% CI:3.008 ~ 19.836,P<0.05)和有相关临床症状(RR=7.879,95% CI:2.357 ~ 26.384,P<0.05)是筛查肿瘤标志物升高人员患肿瘤的危险因素.结论 血清肿瘤标记物联合检测对肿瘤筛查人群应答率高,危险因素调查是肿瘤筛查的有效手段.

关 键 词:恶性肿瘤  早期诊断  肿瘤标记物  联合检测

Clinical significicance of tumor markers combined detection in screening for tumor high-risk groups
Abstract:Objective To investigate the clinical value of combined detection of tumor markers in screening malignant tumor high-risk population.Methods 3 766 people with malignant tumor high-risk were tested with corresponding tumor markers CA125,CEA,Cyfra21-1,CA19-9,AFP,NSE,CA72 4,SCC,CA153 were rised.These people were inspected with cervico thoracicor,abdominal,and pelvic CT or endoscopy.Moreover,these women were followed up for more than 6 months.Results After follow-up,there were 69 cancer patients were found.Among them,20 cases (62.5 %) were diagnosed in 6 months with rised tumor markers,Five cases(15.9%) were diagosed as cancer in 6 months to 1 year.Four cases (12.5%) were diagosed in 1 to 2 years,and two cases (9.4%) were diagosed in 2 to 3 years.COX analysis showed that the degree of the elevated tumor markers (RR =2.308,95% CI:2.517 ~ 2.475,P < 0.001).The gradually increased tumor markers (RR =7.727,95% CI:3.008-19.836,P < 0.05),and relevant symptoms (RR =7.879,95% CI:2.357-26.384,P < 0.05) were the cancer risk factors.Conclusion Combined detection of serum tumor markers is an efficient methed in tumor screening.
Keywords:Cancer  Early detetion  Tumor markers  Combined detection
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