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临床试验/NCT03024398
NCT03024398招募中不适用

Evaluation of the Fluorescent Green of Indocyanine in the Detection of Sentinel Lymph Node in Endometrial Cancer

University Hospital, Strasbourg, France1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2017年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
50
试验地点
1
主要终点
Detection of sentinel node

研究概览

简要总结

Selective lymphadenectomy Sentinel (LSS). This technique is already well established in breast cancer and melanoma and more recently in vulvar and cervical cancer.

Compared to lymphadenectomy, it has several theoretical advantages:

  • this is a sensitive technique with a detection rate of> 90% and a false negative rate of <5%.
  • the anatomopathological techniques used (immunohistochemistry with anti-cytokeratin antibodies, serial sections) are more sensitive than the standard histological analysis of lymphadenectomy, which allows an improvement in the detection of metastases (micro-metastases, isolated tumor cells). In the SENTI-ENDO study, it was possible to detect lymph node metastases in 11% of patients with low-risk endometrial cancer and in 15% of intermediate-risk patients.
  • it avoids short-term and long-term operative and post-operative morbidity of lymphadenectomy.

Early studies of LSS in endometrial cancer demonstrated superior efficacy of the colorimetric method coupled with the Technetium 99m isotopic method with an overall detection rate of 78% [95% CI: 73-84]. The fluorescent green of indocyanine appears to give better results with an overall detection rate of 94% and a bilateral detection rate of 80%.

It seemed useful to take stock of this technique using this new dye.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
Female
接受健康志愿者

入选标准

  • Major patient, without guardianship or curatorship.
  • patient with endometrial cancer confirmed by biopsy.
  • Invasive cancer stage FIGO I at intermediate risk and high risk and II according to the FIGO classification.
  • need for surgical staging.
  • performing an endovaginal ultrasound or a pelvic MRI in preoperative, if contraindication to MRI, performing a CT scan.
  • subject affiliated to a social health insurance scheme.
  • speaking and reading French.
  • subject having dated and signed informed consent.

排除标准

  • pregnancy in progress.
  • FIGO III and IV stage diagnosed preoperatively or intraoperatively.
  • Cure or pre-surgery that may alter the uterine lymphatic drainage (conization, myomectomy).
  • MRI or CT scan of suspected lymph nodes.

结局指标

主要结局

Detection of sentinel node

时间窗: 1 hour after surgery

次要结局

未报告次要终点

研究者

发起方
University Hospital, Strasbourg, France
申办方类型
Other
责任方
Sponsor

研究点 (1)

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