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NCT Number: NCT04845828

Randomized Comparison Between Sentinel Lymph Node Biopsy and Lymph Node Dissection in Early Stage Endometrial Cancer

Through this clinical trial, the investigators aim to verify the usefulness and stability of sentinel lymph node mapping in endometrial cancer of clinical stage I-II.

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Key information

Age range

20 year–80 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

Asan Medical Center

Seoul, South Korea

Location status: Recruiting

Location contact

Jeong-Yeol Park

CONTACT

About this study

The standard treatment for endometrial cancer is total hysterectomy and bilateral salpingo-oophorectomy, peritoneal cytology, and lymph node dissection. Pelvic lymph node dissection helps to set accurate staging and adjuvant therapy group, but it has never been proven to have therapeutic effects by itself. According to the results of two recent randomized clinical trials, routine pelvic lymph node dissection in early stage endometrial cancer doesn't improve survival rates.

Routine pelvic lymph node detection can cause complications in a large number of patients and is associated with poor quality of life. Therefore, it is important to develop a method that can check the status of the lymph node in a less invasive way. Efforts have been made to preserve other lymph nodes with significantly less potential for metastasis through less invasive methods, reducing lymph edema and complications such as bleeding and nerve damage caused by excessive surgery.

Sentinel lymph node dissection is used as a standard treatment for breast cancer and malignant melanoma, and efforts to develop it have recently continued in endometrial cancer and cervical cancer. A SENTICOL study conducted in cervical cancer patients showed a false-negative rate of 0% when both were monitored lymph node dissection. In addition, unlike routine pelvic lymph node dissection, ultra-staging through 0,2mm gas intercepts allow additional detection of less than 2mm of microtransfer or less than 0.2mm of independent tumor cells that have not been found before. In a recent large-scale prospective study of endometrial cancer, sentinel lymph node mapping using indocyanine green and fluorescent imaging was successful at 86%, and sensitivity (patient-by-patient analysis) reported 100% in diagnosis of lymph node metastasis.

As laparoscopic and robotic surgery account for most of the treatment of endometrial cancer patients, a good environment is created for monitoring lymph node exploration using ICG, and sensitivity and detection rate seem to have improved compared to the previous method. However, there has been no prospective study on the effects of patient clinical prognosis, such as a standard treatment, pelvic lymph node resection, and disease-free survival rate, and overall survival rate, so a prospective study is essential. The investigators compare survival rates in the group that does sentinel lymph node mapping and routine pelvic lymph node detection in endometrial cancer in clinical stage I-II.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 20 ~ 80 years old female
  • histologically diagnosed endometrial cancer that has never been treated before.
  • histological type :endometrioid, mucinous, serous, clear cell, uindifferentiated, dedifferentiated, mesonephric adenocarcinoma, mesonephric-like adenocarcinoma, carcinosarcoma, and mixed type
  • histological grade : FIGO grade 1, 2, 3
  • Presumed FIGO stage I-II
  • Planed for laparoscopic or robotic hystererctomy and lymph adenectomy
  • Largest pelvic or para-aortic lymph node diameter = or < 15 mm in short axis on MRI
  • ECOG performance status 0-2
  • ASA PS 0-2
  • WBC ≥ 3,000/mm3, Platelets ≥ 100,000/mm3, Creatinine ≤ 2.0 mg/dL ,Bilirubin ≤ 1.5 x institutional upper limit normal ,SGOT, SGPT, and ALP ≤ 3 x institutional upper limit normal
  • A patient who voluntarily signed a document for the study.

Exclusion criteria

  • Presumed FIGO stage III-IV
  • Neuroendocrine tumor histology
  • Other disease involving lymphatic system
  • lymphedema of the lower extremity or inguinal area
  • previous pelvic or paraaortic lymph node dissection
  • previous radiation or concurrent chemoradiation therapy of abdomen or pelvis
  • previous chemotherapy due to malignant disease of abdomen or pelvis
  • Patients who have had or have been treated for cancer within five years, other than non-melanoma skin cancer, carcinoma in situ of uterine cervix, stomach or bladder
  • severe, uncontrolled underlying diseases or underlying disease with complications
  • hypersensitivity to indocyanine green
  • a pregnant or breast-feeding woman

Treatment and study plan

sentinel lymph node mapping

Procedure

Laparoscopic or robotic hysterectomy with/without bilateral salpingo-oophorectomy 2. Inject 1.25 mg/ml of ICG and a total of 6ml into the cornual area (0.5-1 cm deep) of the uterus. And then inject 1 ml of mucous membrane (1-3 mm deep) and 1 ml of substrate (1-2 cm deep) into the cervix, and a total of 4 ml in each direction of 3 and 9 o'clock.

  • Sentinel lymph node is excised

Other names: Indocyanine green, Fluorescent camera

Routine lymph node dissection

Procedure
  • Laparoscopic or robotic hysterectomy with/without bilateral salpingo-oophorectomy
  • Lymph node detection is performed.

Primary outcomes

  1. The 3-year disease-free survival (3-year DFS)

    Time frame: 3 years

    The time interval between the date of surgery and the date of recurrence will be caculated as month. The survival curve will be calculated suing Kaplan-Meir method, and survival difference will be compared using Log-rank test.

Secondary outcomes

  1. Surgery-related morbidity rate

    Time frame: One month

    Compare the surgery-related morbidity rate after one month of surgery.

  2. Incidence of lymphocele and lymphedema

    Time frame: 3 years

    After 3 years of surgery, the incidence of lymphocele and lymphedema are compared.

  3. The 3-year overall survival (3-year OS)

    Time frame: 3 years

    The time interval between the date of surgery and the date of death of disease will be caculated as month. The survival curve will be calculated suing Kaplan-Meir method, and survival difference will be compared using Log-rank test.

  4. The 5-year disease free survival (5-year DFS)

    Time frame: 5 years

    The time interval between the date of surgery and the date of recurrence will be caculated as month. The survival curve will be calculated suing Kaplan-Meir method, and survival difference will be compared using Log-rank test.

  5. The 5-year overall survival (5-year OS)

    Time frame: 5-years

    The time interval between the date of surgery and the date of death of disease will be caculated as month. The survival curve will be calculated suing Kaplan-Meir method, and survival difference will be compared using Log-rank test.

  6. The pattern of recurrence

    Time frame: 3 years

    Anatomic location of first recurrence

Study contacts

Contact information is provided by the study sponsor or research team.

Jeong-Yeol Park, M.D Ph.D.,

CONTACT

[email protected]

+82-2-3010-3646

Sponsors and collaborators

Lead sponsor

Asan Medical Center

Other

Registry information

Official study title

Prospective Randomized Comparison of Sentinel Lymph Node Mapping Using Indocyanine Green and Conventional Pelvic Lymph Node Dissection in Clinical Stage I-II Endometrial Cancer

Acronym: SELYE

Important dates

Study start
2022
Primary completion
2027
Study completion
2029
First posted
Apr 15, 2021
Registry last updated
Feb 21, 2022

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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