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

Primary Purpose

Endometrial Cancer

Status
Recruiting
Phase
Not Applicable
Locations
Korea, Republic of
Study Type
Interventional
Intervention
Sentinel lymph node mapping
Routine lymph node dissection
Sponsored by
Asan Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endometrial Cancer focused on measuring Sentinel lymph node mapping, Indocyanine green, Fluorescent camera, Lymph node dissection, Endometrial cancer

Eligibility Criteria

20 Years - 80 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. 20 ~ 80 years old female
  2. histologically diagnosed endometrial cancer that has never been treated before.
  3. histological type :endometrioid, mucinous, serous, clear cell, uindifferentiated, dedifferentiated, mesonephric adenocarcinoma, mesonephric-like adenocarcinoma, carcinosarcoma, and mixed type
  4. histological grade : FIGO grade 1, 2, 3
  5. Presumed FIGO stage I-II
  6. Planed for laparoscopic or robotic hystererctomy and lymph adenectomy
  7. Largest pelvic or para-aortic lymph node diameter = or < 15 mm in short axis on MRI
  8. ECOG performance status 0-2
  9. ASA PS 0-2
  10. 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
  11. A patient who voluntarily signed a document for the study.

Exclusion Criteria:

  1. Presumed FIGO stage III-IV
  2. Neuroendocrine tumor histology
  3. Other disease involving lymphatic system
  4. lymphedema of the lower extremity or inguinal area
  5. previous pelvic or paraaortic lymph node dissection
  6. previous radiation or concurrent chemoradiation therapy of abdomen or pelvis
  7. previous chemotherapy due to malignant disease of abdomen or pelvis
  8. 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
  9. severe, uncontrolled underlying diseases or underlying disease with complications
  10. hypersensitivity to indocyanine green
  11. a pregnant or breast-feeding woman

Sites / Locations

  • Asan Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Sentinel lymph node mapping

Routine lymph node dissection

Arm Description

The group composed of patients who undergo sentinel lymph node mapping

The group composed of patients who undergo routine pelvic lymph node dissection

Outcomes

Primary Outcome Measures

The 3-year disease-free survival (3-year DFS)
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 Outcome Measures

Surgery-related morbidity rate
Compare the surgery-related morbidity rate after one month of surgery.
Incidence of lymphocele and lymphedema
After 3 years of surgery, the incidence of lymphocele and lymphedema are compared.
The 3-year overall survival (3-year OS)
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.
The 5-year disease free survival (5-year DFS)
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.
The 5-year overall survival (5-year OS)
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.
The pattern of recurrence
Anatomic location of first recurrence

Full Information

First Posted
April 12, 2021
Last Updated
February 18, 2022
Sponsor
Asan Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT04845828
Brief Title
Randomized Comparison Between Sentinel Lymph Node Biopsy and Lymph Node Dissection in Early Stage Endometrial Cancer
Acronym
SELYE
Official 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
Study Type
Interventional

2. Study Status

Record Verification Date
February 2022
Overall Recruitment Status
Recruiting
Study Start Date
January 26, 2022 (Actual)
Primary Completion Date
December 1, 2027 (Anticipated)
Study Completion Date
December 1, 2029 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Asan Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
Yes
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometrial Cancer
Keywords
Sentinel lymph node mapping, Indocyanine green, Fluorescent camera, Lymph node dissection, Endometrial cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantOutcomes Assessor
Allocation
Randomized
Enrollment
810 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Sentinel lymph node mapping
Arm Type
Experimental
Arm Description
The group composed of patients who undergo sentinel lymph node mapping
Arm Title
Routine lymph node dissection
Arm Type
Active Comparator
Arm Description
The group composed of patients who undergo routine pelvic lymph node dissection
Intervention Type
Procedure
Intervention Name(s)
Sentinel lymph node mapping
Other Intervention Name(s)
Indocyanine green, Fluorescent camera
Intervention Description
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. 3. Sentinel lymph node is excised
Intervention Type
Procedure
Intervention Name(s)
Routine lymph node dissection
Intervention Description
Laparoscopic or robotic hysterectomy with/without bilateral salpingo-oophorectomy Lymph node detection is performed.
Primary Outcome Measure Information:
Title
The 3-year disease-free survival (3-year DFS)
Description
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.
Time Frame
3 years
Secondary Outcome Measure Information:
Title
Surgery-related morbidity rate
Description
Compare the surgery-related morbidity rate after one month of surgery.
Time Frame
One month
Title
Incidence of lymphocele and lymphedema
Description
After 3 years of surgery, the incidence of lymphocele and lymphedema are compared.
Time Frame
3 years
Title
The 3-year overall survival (3-year OS)
Description
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.
Time Frame
3 years
Title
The 5-year disease free survival (5-year DFS)
Description
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.
Time Frame
5 years
Title
The 5-year overall survival (5-year OS)
Description
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.
Time Frame
5-years
Title
The pattern of recurrence
Description
Anatomic location of first recurrence
Time Frame
3 years

10. Eligibility

Sex
Female
Gender Based
Yes
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jeong-Yeol Park, M.D Ph.D.,
Phone
+82-2-3010-3646
Email
obgyjypark@amc.seoul.kr
Facility Information:
Facility Name
Asan Medical Center
City
Seoul
Country
Korea, Republic of
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jeong-Yeol Park

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
21444878
Citation
Lecuru F, Mathevet P, Querleu D, Leblanc E, Morice P, Darai E, Marret H, Magaud L, Gillaizeau F, Chatellier G, Dargent D. Bilateral negative sentinel nodes accurately predict absence of lymph node metastasis in early cervical cancer: results of the SENTICOL study. J Clin Oncol. 2011 May 1;29(13):1686-91. doi: 10.1200/JCO.2010.32.0432. Epub 2011 Mar 28.
Results Reference
background
PubMed Identifier
21489874
Citation
Ballester M, Dubernard G, Lecuru F, Heitz D, Mathevet P, Marret H, Querleu D, Golfier F, Leblanc E, Rouzier R, Darai E. Detection rate and diagnostic accuracy of sentinel-node biopsy in early stage endometrial cancer: a prospective multicentre study (SENTI-ENDO). Lancet Oncol. 2011 May;12(5):469-76. doi: 10.1016/S1470-2045(11)70070-5. Epub 2011 Apr 12.
Results Reference
background
PubMed Identifier
25986870
Citation
Bae HS, Lim MC, Lee JS, Lee Y, Nam BH, Seo SS, Kang S, Chung SH, Kim JY, Park SY. Postoperative Lower Extremity Edema in Patients with Primary Endometrial Cancer. Ann Surg Oncol. 2016 Jan;23(1):186-95. doi: 10.1245/s10434-015-4613-1. Epub 2015 May 19.
Results Reference
background
PubMed Identifier
26095896
Citation
Tanner EJ, Sinno AK, Stone RL, Levinson KL, Long KC, Fader AN. Factors associated with successful bilateral sentinel lymph node mapping in endometrial cancer. Gynecol Oncol. 2015 Sep;138(3):542-7. doi: 10.1016/j.ygyno.2015.06.024. Epub 2015 Jun 19.
Results Reference
background
PubMed Identifier
36047376
Citation
Park JY, Kim JH, Baek MH, Park E, Kim SW. Randomized comparison between sentinel lymph node mapping using indocyanine green plus a fluorescent camera versus lymph node dissection in clinical stage I-II endometrial cancer: a Korean Gynecologic Oncology Group trial (KGOG2029/SELYE). J Gynecol Oncol. 2022 Nov;33(6):e73. doi: 10.3802/jgo.2022.33.e73. Epub 2022 Jul 25.
Results Reference
derived

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

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