中华检验医学杂志
中華檢驗醫學雜誌
중화검험의학잡지
CHINESE JOURNAL OF LABORATORY MEDICINE
2015年
2期
106-110
,共5页
陈欢欢%潘世扬%张洁心%张燕%黄珮珺%黄蕾%王加%凌芸%高丽
陳歡歡%潘世颺%張潔心%張燕%黃珮珺%黃蕾%王加%凌蕓%高麗
진환환%반세양%장길심%장연%황패군%황뢰%왕가%릉예%고려
癌,非小细胞肺%胸腔积液%流式细胞术
癌,非小細胞肺%胸腔積液%流式細胞術
암,비소세포폐%흉강적액%류식세포술
Carcinoma,non-small-cell lung%Pleural effusion%Flow cytometry
目的 探讨特异性荧光抗体标记的流式细胞术检测胸腔积液肺癌脱落细胞的临床应用价值.方法 采用特异性识别非小细胞肺癌(NSCLC)的单克隆抗体NJ001进行荧光标记,建立流式细胞术检测胸腔积液肺癌脱落细胞的方法.采用病例对照研究,收集2014年2至8月南京医科大学第一附属医院经临床确诊的32例NSCLC(包括29例肺腺癌和3例肺鳞癌)和26例肺部良性疾病患者的胸腔积液,流式细胞术进行肺癌脱落细胞水平检测,采用秩和检验分析组间差异,并绘制ROC曲线进行分析;对32例NSCLC的流式法和巴氏染色法检测结果进行x2检验统计比较.对22例NSCLC胸腔积液脱落细胞涂片采用直接荧光法检测,观察脱落细胞上NJ001特异性抗原的表达,并与流式法检测结果进行x2检验统计比较.结果 NSCLC组流式检测的阳性计数水平为100(2 ~988)个/10万,显著高于肺部良性疾病组的5(0~18)个/10万(Z=-5.647,P<0.001);ROC曲线下面积为0.934;最佳诊断临界值为18个/10万,对应的敏感度为87.5% (28/32),特异度为100.0%(26/26).其中29例肺腺癌胸腔积液流式法检测的阳性率为93.1%(27/29),显著高于巴氏染色法检测的阳性率58.6%(17/29),差异有统计学意义(x2 =7.627,P=0.006),12例巴氏染色法检测阴性的肺腺癌胸腔积液,流式法检测的阳性率为11/12;3例肺鳞癌胸腔积液流式法检测的阳性率为1/3,对应的巴氏染色法检测均为阴性.22例NSCLC胸腔积液脱落细胞涂片直接荧光法检测的阳性率为59.1% (13/22);对应的流式法的阳性率为90.9%(20/22),显著高于直接荧光法的阳性率59.1%(13/22) (x2 =4.364,P=0.037).结论 特异性荧光抗体标记的流式细胞术检测胸腔积液肺癌尤其是肺腺癌脱落细胞具有极高的敏感度和特异度,具有重要的临床应用价值.
目的 探討特異性熒光抗體標記的流式細胞術檢測胸腔積液肺癌脫落細胞的臨床應用價值.方法 採用特異性識彆非小細胞肺癌(NSCLC)的單剋隆抗體NJ001進行熒光標記,建立流式細胞術檢測胸腔積液肺癌脫落細胞的方法.採用病例對照研究,收集2014年2至8月南京醫科大學第一附屬醫院經臨床確診的32例NSCLC(包括29例肺腺癌和3例肺鱗癌)和26例肺部良性疾病患者的胸腔積液,流式細胞術進行肺癌脫落細胞水平檢測,採用秩和檢驗分析組間差異,併繪製ROC麯線進行分析;對32例NSCLC的流式法和巴氏染色法檢測結果進行x2檢驗統計比較.對22例NSCLC胸腔積液脫落細胞塗片採用直接熒光法檢測,觀察脫落細胞上NJ001特異性抗原的錶達,併與流式法檢測結果進行x2檢驗統計比較.結果 NSCLC組流式檢測的暘性計數水平為100(2 ~988)箇/10萬,顯著高于肺部良性疾病組的5(0~18)箇/10萬(Z=-5.647,P<0.001);ROC麯線下麵積為0.934;最佳診斷臨界值為18箇/10萬,對應的敏感度為87.5% (28/32),特異度為100.0%(26/26).其中29例肺腺癌胸腔積液流式法檢測的暘性率為93.1%(27/29),顯著高于巴氏染色法檢測的暘性率58.6%(17/29),差異有統計學意義(x2 =7.627,P=0.006),12例巴氏染色法檢測陰性的肺腺癌胸腔積液,流式法檢測的暘性率為11/12;3例肺鱗癌胸腔積液流式法檢測的暘性率為1/3,對應的巴氏染色法檢測均為陰性.22例NSCLC胸腔積液脫落細胞塗片直接熒光法檢測的暘性率為59.1% (13/22);對應的流式法的暘性率為90.9%(20/22),顯著高于直接熒光法的暘性率59.1%(13/22) (x2 =4.364,P=0.037).結論 特異性熒光抗體標記的流式細胞術檢測胸腔積液肺癌尤其是肺腺癌脫落細胞具有極高的敏感度和特異度,具有重要的臨床應用價值.
목적 탐토특이성형광항체표기적류식세포술검측흉강적액폐암탈락세포적림상응용개치.방법 채용특이성식별비소세포폐암(NSCLC)적단극륭항체NJ001진행형광표기,건립류식세포술검측흉강적액폐암탈락세포적방법.채용병례대조연구,수집2014년2지8월남경의과대학제일부속의원경림상학진적32례NSCLC(포괄29례폐선암화3례폐린암)화26례폐부량성질병환자적흉강적액,류식세포술진행폐암탈락세포수평검측,채용질화검험분석조간차이,병회제ROC곡선진행분석;대32례NSCLC적류식법화파씨염색법검측결과진행x2검험통계비교.대22례NSCLC흉강적액탈락세포도편채용직접형광법검측,관찰탈락세포상NJ001특이성항원적표체,병여류식법검측결과진행x2검험통계비교.결과 NSCLC조류식검측적양성계수수평위100(2 ~988)개/10만,현저고우폐부량성질병조적5(0~18)개/10만(Z=-5.647,P<0.001);ROC곡선하면적위0.934;최가진단림계치위18개/10만,대응적민감도위87.5% (28/32),특이도위100.0%(26/26).기중29례폐선암흉강적액류식법검측적양성솔위93.1%(27/29),현저고우파씨염색법검측적양성솔58.6%(17/29),차이유통계학의의(x2 =7.627,P=0.006),12례파씨염색법검측음성적폐선암흉강적액,류식법검측적양성솔위11/12;3례폐린암흉강적액류식법검측적양성솔위1/3,대응적파씨염색법검측균위음성.22례NSCLC흉강적액탈락세포도편직접형광법검측적양성솔위59.1% (13/22);대응적류식법적양성솔위90.9%(20/22),현저고우직접형광법적양성솔59.1%(13/22) (x2 =4.364,P=0.037).결론 특이성형광항체표기적류식세포술검측흉강적액폐암우기시폐선암탈락세포구유겁고적민감도화특이도,구유중요적림상응용개치.
Objective To investigate the clinical application value of flow cytometry (FCM) established by specific fluorescent monoclonal antibody in detecting lung cancer cells in pleural effusion with non-small cell lung cancer (NSCLC).Methods The FCM assay was established by using fluorescent monoclonal antibody NJ001 which could specifically recognize NSCLC.A case-control study was conducted to evaluate the level of lung cancer cells in pleural effusion among 32 cases of NSCLC (including 29 lung adenocarcinoma cases and 3 lung squamous cell carcinoma cases) and 26 cases of benign disease with definite diagnosis collected from the First Affiliated Hospital of Nanjing Medical University from February 2014 to August 2014.The data of FCM assay between NSCLC and benign disease were evaluated by the rank sum test.The data were analyzed by ROC curve to assess the diagnosis value.Those FCM results among 32 cases of NSCLC were compared with Papanicolaou staining by the chi-square test.Meanwhile,NJ001 specific antigen on exfoliate cells was detected by direct immunofluorescence assay and comparing with FCM assay by the chi-square test among 22 cases of NSCLC.Results The number of positive events by FCM assay was 5(0-18)/100 000 in benign pleural effusion and 100(2-988)/100 000 in pleural effusion of NSCLC,which was significantly higher compared with the benign disease (Z =-5.647,P < 0.001).The area under the ROC curve was 0.934 and the optimal diagnostic critical value was 18/100 000.This method performed a high sensitivity[87.5% (28/32)] and specificity[100.0% (26/26)].The positive rate in 29 lung adenocarcinoma cases was significantly higher by FCM assay than Papanicolaou staining [93.1% (27/ 29) vs 58.6% (17/29),x2 =7.627,P =0.006],and in 12 negative Papanicolaou staining lung adenocarcinoma cases the positive rate of FCM assay was 11/12; In 3 lung squamous cell carcinoma cases the positive rate of FCM assay was 1/3 while all of Papanicolaou staining presented negative results.The FCM assay positive rate of 22 NSCLC cases was significantly higher than the direct immunofluorescence assay [90.9% (20/22) vs 59.1% (13/22),x2 =4.364,P =0.037].Conclusion The FCM assay established by specific fluorescent monoclonal antibody applied for lung cancer cells especially for lung adenocarcinoma detection in pleural effusion had a high sensitivity and specificity,which was confirmed to be a valuable technological application for NSCLC clinical diagnosis.