Evaluation of the Efficacy for Sentinel Lymph Node Policy in Intermediate-risk Endometrial Carcinomas

Sponsor
Fudan University (Other)
Overall Status
Withdrawn
CT.gov ID
NCT03677024
Collaborator
(none)
0
1
2
20
0

Study Details

Study Description

Brief Summary

To evaluate the efficacy of sentinel lymph node policy in patients with intermediate-risk endometrial carcinomas

Condition or Disease Intervention/Treatment Phase
  • Procedure: SLN arm
N/A

Detailed Description

Surgical assessment for staging of endometrial carcinoma during primary surgery remains one of the most varied practices worldwide, as it may include no nodal assessment, sentinel node mapping, and complete pelvic and aortic lymphadenectomy up to the renal vessels. Since lymphadenectomy is significantly associated with longer operating time, higher surgical costs, greater rate of infection, as well as the occurrence of lymphocysts and lymphedema, gynecologists agree that pelvic and aortic lymphadenectomy should be routinely performed in high-risk patients (grade 3, deep myometrial invasion, type 2 cancer). However, whether lymphadenectomy is required in patients with endometrioid endometrial cancers of grade 1 or 2 and with less than 50% myometrial invasion is controversial. Then, the investigators conducted this prospective cohort study to investigate the efficacy of sentinel lymph node policy in patients with intermediate-risk endometrial carcinomas (grade 1 or 2, < 50% myometrial invasion, and a tumor diameter ≥ 2 cm) as well as their outcomes.

Surgery should be performed within a maximum of 4 weeks from the patient's first consultation.

Study Design

Study Type:
Interventional
Actual Enrollment :
0 participants
Allocation:
Non-Randomized
Intervention Model:
Crossover Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Evaluation of the Efficacy for Sentinel Lymph Node Policy in Intermediate-risk Endometrial Carcinomas
Anticipated Study Start Date :
Feb 6, 2020
Anticipated Primary Completion Date :
Oct 7, 2021
Anticipated Study Completion Date :
Oct 7, 2021

Arms and Interventions

Arm Intervention/Treatment
Experimental: SLN arm

Experimental: Intra-operative sentinel lymph node (SLN) mapping with indocyanin green injected into the stroma of the cervix. Full bilateral laparoscopic lymphadenectomy and hysterectomy: If bilateral SLN are detected, all positive SLN will be removed. Then the surgeons proceeds to a total hysterectomy. If only unilateral SLN are detected, surgeons will proceed to pelvic lymphadenectomy on the opposite side. If non SLN are detected, surgeons will proceed to a total hysterectomy, a bilateral salpingo-oophorectomy, a complete and bilateral pelvic lymphadenectomy.

Procedure: SLN arm
Intra-operative SN mapping with indocyanin green: Intracervical injection will be performed by the surgeon. Sub-mucous injections will be performed with 50% diluted dye at 3 and 9 o'clock positions. 1ml injection contained infracyanine green will be injected deeply into the stroma of the cervix (1cm-depth), and another 1ml will be injected superficially (2mm-depth). The time between the injection and the search for SLN must be as soon as possible.

No Intervention: Lymphadenectomy arm

Surgeons will proceed to a total hysterectomy, a bilateral salpingo-oophorectomy, a complete and bilateral pelvic lymphadenectomy.

Outcome Measures

Primary Outcome Measures

  1. Performance Analysis [Within 14 days after the surgery]

    Using the final pathological diagnosis as the Gold Standard, the investigators will calculate the sensitivity, specificity, and predictive accuracy of mapping and detection of SLN with metastatic disease.

Secondary Outcome Measures

  1. Postoperative complications [1 years after the surgery]

    Comparison of the incidence of complications such as lymph cysts, lymph edema, and postoperative fever etc.

  2. Recurrence rate [5 years after the surgery]

    The recurrence rate of different groups will be followed up.

  3. Adjuvant therapy rate [5 years after the surgery]

    The adjuvant therapy rate of different groups will be followed up.

  4. 5-year survival rate [5 years after the surgery]

    The 5-year survival rate of different groups will be followed up.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 100 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Age ≥ 18 years.

  2. No contraindication to surgery.

  3. Signed and dated informed consent.

  4. Intermediate-risk endometrioid cancer with grade 1-2, superficial myometrial invasion and tumor diameter ≥ 2cm (in intraoperative frozen section examinations).

  5. Without any suspicious pelvic, paraaortic or distant lymph node metastasis in preoperative imaging tests including MRI/CT/PET-CT.

Exclusion Criteria:
  1. Low-risk endometrioid cancer with grade 1-2, superficial myometrial invasion and tumor diameter < 2cm (in intraoperative frozen section examinations).

  2. Grade 3 endometrioid cancer (in preoperative pathological diagnosis or in intraoperative frozen section examinations).

  3. Deep muscular infiltration (in intraoperative frozen section examinations).

  4. Cervical invasion and/or ovarian/tubal invasion (in intraoperative frozen section examinations).

  5. With suspicious pelvic, paraaortic or distant lymph node metastasis in preoperative imaging tests including MRI/CT/PET-CT.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Obstetrics and Gynecology Hospital, Fudan University Shanghai Shanghai China 200011

Sponsors and Collaborators

  • Fudan University

Investigators

  • Principal Investigator: Xiaojun Chen, PhD, Obstetrics and Gynecology Hospital, Fudan University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Xiaojun Chen, Principal Investigator, Fudan University
ClinicalTrials.gov Identifier:
NCT03677024
Other Study ID Numbers:
  • 53201012
First Posted:
Sep 19, 2018
Last Update Posted:
Feb 5, 2020
Last Verified:
Feb 1, 2020
Individual Participant Data (IPD) Sharing Statement:
Undecided
Plan to Share IPD:
Undecided
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Xiaojun Chen, Principal Investigator, Fudan University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Feb 5, 2020