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Intraoperative sentinel lymph node mapping in stage I non-small cell lung cancer: detection of micrometastases by polymerase chain reaction

机译:Ⅰ期非小细胞肺癌的术中前哨淋巴结定位:通过聚合酶链反应检测微小转移

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Objective: We previously reported the results achieved in detecting sentinel lymph nodes (SLN). We applied the molecular techniques (RT-PCR) to improve the detection of micrometastasis in order to evaluate an improvement of staging in early non-small cell lung cancer (NSCLC) patients (pts). Methods: This study was carried out on 22 consecutive NSCLC pts with stage I disease. A dose of 37 MBq (1 ml 99mTc-nanocolloid® suspension) was administered. The intralesional injection was performed under CT-guidance (7 pts), by using bronchoscopy (5 pts), VATS (2 pts) and at time of the thoracotomy (8 pts). RT-PCR analysis for cytokeratin 7 and 19 (CK7-CK19) was used to identify tumour-derived material in lymph nodes (LN). Each SLN was bisected: half was used for conventional examination (H&E staining/by immunohistochemistry (IHC), half was snap-frozen to -80 °C for RNA-detection of CK7 and CK19. Results: SLN was detected in 16 out of 19 pts. In three pts SLN was not identified (due to an incorrect technique). Conventional pathologic examination showed stage I disease in 13 pts, T3N0 disease in 1 pt, N2 in 5 pts. The IHC analysis identified micrometastasis in seven pts (two evaluated N0 according to H&E staining). RT-PCR analysis, performed in 10/16 pts, identified micrometastasis in 6 pts (3 pts evaluated N0 disease by H&E; 1 of these evaluated N0 even by IHC). All N2 patients relapsed. One patient (N0 pts after H&E and IHC analysis) with positive CK7 and CK19 expression by RT-PCR analysis relapsed (systemic relapse) 3 months after surgery. Conclusions: SLN technique could provide a subgroup of patients in which the use of RT-PCR could be applied on a well-focused target. This approach may be useful for stratifying histologically N0 patients into higher risk and lower risk groups. © 2008 European Association for Cardio-Thoracic Surgery
机译:目的:我们先前报道了在检测前哨淋巴结(SLN)方面取得的成果。我们应用了分子技术(RT-PCR)来改善微转移的检测,以评估早期非小细胞肺癌(NSCLC)患者的分期改善情况(pts)。方法:本研究针对22例患有I期疾病的非小细胞肺癌患者进行。给药剂量为37 MBq(1 ml 99mTc-nanocolloid?悬浮液)。在CT引导下(7分),使用支气管镜检查(5分),VATS(2分)和开胸手术时(8分)进行病灶内注射。细胞角蛋白7和19(CK7-CK19)的RT-PCR分析用于鉴定淋巴结(LN)中的肿瘤来源物质。每个SLN均一分为二:一半用于常规检查(H&E染色/免疫组织化学(IHC),一半冷冻至-80°C,用于CK7和CK19的RNA检测。结果:在19个中有16个检测到SLN在3分中,未鉴定出SLN(由于技术不正确);常规病理检查显示I期疾病为13分,T3N0疾病为1分,N2为5分。IHC分析鉴定为7分的微转移(评估为2分)根据H&E染色N0),以10/16 pts进行RT-PCR分析,发现6 pts有微转移(H&E评估N0疾病3 pts;甚至IHC评估N0疾病中1例)N2全部复发,1例患者复发。 RT-PCR分析显示CK7和CK19阳性表达(H&E和IHC分析后N0分)在术后3个月复发(全身性复发)结论:SLN技术可以为亚组患者提供RT-PCR的可能应用于重点明确的目标。这种方法可能对从组织学角度将N0患者分为高危和低危人群。 ©2008欧洲心胸外科协会

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