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首页> 外文期刊>Canadian Urological Association Journal >Moderated Poster Session V: Oncology/Laparoscopy/Robotics/Basic Science
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Moderated Poster Session V: Oncology/Laparoscopy/Robotics/Basic Science

机译:适度的海报会话V:肿瘤科/腹腔镜/机器人/基础科学

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Background: Local recurrence remains a major cause of cancer-specificmortality following radical cystectomy. We sought to investigate tumordissemination in the operative field and contribution of pneumoperitoneumduring robot-assisted radical cystectomy (RARC).Methods: Six RARCs were included. Four pelvic irrigations with 0.9%normal saline were performed: Sample I: before RARC; Sample II: afterRARC; Sample III: after pelvic lymph node dissection (PLND), and leftoverirrigation fluid at end of procedure (Sample IV). CO2 used for pneumoperitoneumwas filtered using surgical smoke plume evacuation device. Filterwas then removed, washed with 0.9% saline, centrifuged and sedimentwas analyzed. Intravesical bladder irrigations were performed for threepatients. Methodology: pelvic irrigations (SI-IV) were examined for cytologyusing thin preparation and cell block by a genito-urinary pathologist/cytopathologist. Meanwhile, intravesical wash, pelvic irrigation, and filtersediment were analyzed for mRNA expression of bladder cancer relatedgenes. mRNA expression was examined by qRT-PCR, with human bladdercancer cell line 253J and GAPDH (controls). Epithelial cell markers EpCAM,cytokeratins 8, 18, and 19 were also assessed. Bladder cancer gene panelsused in the Cxbladder Detect urinary test were also examined (CDK1, MDK,IGFBP5, HOXA13 and CXCR2).Results: Four patients received neoadjuvant chemotherapy. The meanoperative time was 300 minutes. Four patients had pT1 disease, two hadpT2 disease. All patients had negative soft tissue surgical margins andmean LNY was 31. One patient had positive lymph nodes. No spillageof tumor cells or inadvertent entry into the bladder was observed. Alllymph nodes were removed in specimen bags. Cytology: Pelvic Irrigationshowed mostly blood, inflammatory, mesothelial cells and macrophages.All specimens were negative for malignant cells. mRNA expression: Bladdercancer-related mRNA was detected in the intra-vesical wash and 253Jbladder cancer cells (control). In contrast, all pelvic irrigations and filtersediment had very low or undetectable mRNA levels. However, in patientwith node positive disease, SI irrigation showed many epithelial markers(KRT8, 18, 19, IGFBP5).Conclusions: Our preliminary analysis showed that bladder cancer cells,bladder cancer-related genes and epithelial markers were not present inpelvic irrigation but in intravesical wash. These cells were detected in thepelvis in one patient with advanced disease. Active enrollment in this studycontinues, which will allow better understanding of local spread of bladdercancer. Funding by Roswell Park Alliance Foundation.
机译:背景:局部复发仍然是自由基膀胱切除术后癌症特异性的主要原因。我们试图调查手术域中的肿瘤术和肺肺型机器人辅助自由基膀胱切除术(RARC)的贡献。方法:包括六个RARC。进行四种骨盆灌溉,伴有0.9%生理盐水:样品I:在RARC之前;样本II:追逐;样品III:盆腔淋巴结解剖(PLND)和过程结束时的剩余灌浆液(样品IV)。 CO2用于使用外科烟雾羽状疏散装置过滤的气球。然后除去滤液,用0.9%盐水洗涤,分析离心和沉积物。对三间植物进行膀胱内膀胱灌溉。方法:通过泌尿细胞病理学家/细胞病理学医生检查细胞学薄制剂和细胞嵌段的骨盆灌溉(Si-IV)。同时,分析了膀胱内洗涤,盆腔灌溉和滤液,用于膀胱癌相关的mRNA表达。用QRT-PCR检查mRNA表达,用人膀胱癌细胞系253J和GAPDH(对照)。还评估上皮细胞标志物EPCAM,细胞角蛋白8,18和19。还检查了CxBladder检测尿检测中的膀胱癌基因(CDK1,MDK,IGFBP5,HOXA13和CXCR2)。结果:4名患者接受Neoadjuvant化疗。班次时间为300分钟。四名患者有PT1疾病,两只HADPT2疾病。所有患者患有阴性软组织外科山羊和艾氏患者31.一名患者有阳性淋巴结。没有观察到肿瘤细胞或无意中进入膀胱进入膀胱。在样品袋中除去全文节点。细胞学:盆腔灌溉主要是血液,炎症,间皮细胞和巨噬细胞。所有标本对恶性细胞负是阴性的。 MRNA表达:在血清内洗涤和253JBLADDER癌细胞(对照)中检测到膀胱癌相关mRNA。相比之下,所有盆腔灌溉和滤液都具有非常低或不可检测的mRNA水平。但是,在患者节点阳性疾病中,SI灌溉显示出许多上皮标记(KRT8,18,19,IGFBP5)。结论:我们的初步分析表明膀胱癌细胞,膀胱癌相关基因和上皮标记物均未出现inlosphiC灌溉,但在膀胱内洗涤。在具有晚期疾病的一名患者的患者中检测到这些细胞。本研究中的积极注册,这将使膀胱癌的当地传播更好地了解。 Roswell Park Alliance Foundation的资金。

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