首页> 外文期刊>The lancet oncology >Detection rate and diagnostic accuracy of sentinel-node biopsy in early stage endometrial cancer: a prospective multicentre study (SENTI-ENDO).
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Detection rate and diagnostic accuracy of sentinel-node biopsy in early stage endometrial cancer: a prospective multicentre study (SENTI-ENDO).

机译:早期子宫内膜癌前哨淋巴结活检的检出率和诊断准确性:一项前瞻性多中心研究(SENTI-ENDO)。

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BACKGROUND: Retrospective single-centre series have shown the feasibility of sentinel lymph-node (SLN) identification in endometrial cancer. We did a prospective, multicentre cohort study to assess the detection rate and diagnostic accuracy of the SLN procedure in predicting the pathological pelvic-node status in patients with early stage endometrial cancer. METHODS: Patients with International Federation of Gynecology and Obstetrics (FIGO) stage I-II endometrial cancer had pelvic SLN assessment via cervical dual injection (with technetium and patent blue), and systematic pelvic-node dissection. All lymph nodes were histopathologically examined and SLNs were serial sectioned and examined by immunochemistry. The primary endpoint was estimation of the negative predictive value (NPV) of sentinel-node biopsy per hemipelvis. This is an ongoing study for which recruitment has ended. The study is registered with ClinicalTrials.gov, number NCT00987051. FINDINGS: From July 5, 2007, to Aug 4, 2009, 133 patients were enrolled at nine centres in France. No complications occurred after injection of technetium colloid and no anaphylactic reactions were noted after patent blue injection. No surgical complications were reported during SLN biopsy, including procedures that involved conversion to open surgery. At least one SLN was detected in 111 of the 125 eligible patients. 19 of 111 (17%) had pelvic-lymph-node metastases. Five of 111 patients (5%) had an associated SLN in the para-aortic area. Considering the hemipelvis as the unit of analysis, NPV was 100% (95% CI 95-100) and sensitivity 100% (63-100). Considering the patient as the unit of analysis, three patients had false-negative results (two had metastatic nodes in the contralateral pelvic area and one in the para-aortic area), giving an NPV of 97% (95% CI 91-99) and sensitivity of 84% (62-95). All three of these patients had type 2 endometrial cancer. Immunohistochemistry and serial sectioning detected metastases undiagnosed by conventional histology in nine of 111 (8%) patients with detected SLNs, representing nine of the 19 patients (47%) with metastases. SLN biopsy upstaged 10% of patients with low-risk and 15% of those with intermediate-risk endometrial cancer. INTERPRETATION: SLN biopsy with cervical dual labelling could be a trade-off between systematic lymphadenectomy and no dissection at all in patients with endometrial cancer of low or intermediate risk. Moreover, our study suggests that SLN biopsy could provide important data to tailor adjuvant therapy. FUNDING: Direction Interregionale de Recherche Clinique, Ile-de-France, Assistance Publique-Hopitaux de Paris.
机译:背景:回顾性单中心系列研究已表明前哨淋巴结(SLN)鉴定在子宫内膜癌中的可行性。我们进行了一项前瞻性,多中心队列研究,以评估SLN程序在预测早期子宫内膜癌患者的病理性盆腔结节状态中的检测率和诊断准确性。方法:国际妇产科联合会(I-II期)子宫内膜癌患者通过颈椎双次注射(tech和漆成蓝色)进行盆腔SLN评估,并进行系统的盆腔淋巴结清扫术。对所有淋巴结进行组织病理学检查,并将SLNs连续切片并通过免疫化学检查。主要终点是每半个骨盆前哨淋巴结活检阴性预测值(NPV)的估计。这是一项正在进行的研究,招募已经结束。该研究已在ClinicalTrials.gov上注册,编号为NCT00987051。结果:从2007年7月5日到2009年8月4日,在法国的9个中心招募了133名患者。注射tech胶体后无并发症发生,注射专利蓝后未发现过敏反应。 SLN活检期间未报告手术并发症,包括涉及转为开放手术的手术。在125名合格患者中,至少有111名被检测到SLN。 111人中有19人(17%)有盆腔淋巴结转移。 111名患者中有5名(5%)在主动脉旁区域伴有SLN。以半盆腔为分析单位,NPV为100%(95%CI 95-100),灵敏度为100%(63-100)。以患者为分析单位,三名患者出现假阴性结果(两名在对侧骨盆区域转移,另一名在主动脉旁区域转移),NPV为97%(95%CI 91-99)。和敏感度为84%(62-95)。所有这三例患者均患有2型子宫内膜癌。免疫组织化学和连续切片法检测到111例SLNs中有9例(8%)患者中有9例(47%)有常规组织学无法诊断的转移,占19例(47%)转移中的9例。 SLN活检使低风险的子宫内膜癌患者和低风险的子宫内膜癌患者的比例分别提高了10%和15%。解释:对于具有低或中度风险的子宫内膜癌患者,采用宫颈双重标记的SLN活检可能是在系统性淋巴结清扫术与完全不进行解剖之间的权衡。此外,我们的研究表明,SLN活检可以提供重要的数据来调整辅助治疗。资金来源:法兰西岛大区区域卫生研究所指导,巴黎公共医院。

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