Evaluation of Indocyanine Green-guided Systematic Pelvic Lymphadenectomy in Endometrial and Cervical Cancer

Sponsor
Università degli Studi dell'Insubria (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT04246580
Collaborator
(none)
100
120

Study Details

Study Description

Brief Summary

The lymph nodes involvement is one of the most important prognostic factors in endometrial (EC) and cervical cancer (CC). Indeed, the lymph node involvement in cancer patients modifies the International Federation of Gynecology and Obstetrics (FIGO) stage and plays a pivotal role in the choice of the adjuvant therapy.

Since the modern imaging techniques are not yet able to accurately detect lymph nodes metastasis, pelvic systematic lymphadenectomy has still an important role and it still represents the gold standard in EC and CC. The sentinel lymph node (SLN) biopsy, which is a standard practice in breast cancer and melanoma, is often used in some early stage gynaecological cancers such as EC and CC.

Indocyanine green (ICG) is the most used tracer for the detection of SLN in gynaecological cancer, especially in laparoendoscopic setting. ICG allows a complete visualization of the lymphatic drainage and, for this reason, it may be used even in systematic pelvic lymphadenectomy to guide the surgeon during the procedure. Several studies have demonstrated an advantage of the ICG-guided lymphadenectomy in other types of cancers, showing a higher number of lymph nodes removed with this technique when compared to standard lymphadenectomy (without ICG).

To date, there is no published study about ICG-guided systematic pelvic lymphadenectomy in EC and CC. In this scenario, the aim of this study will be to compare systematic ICG-guided pelvic lymphadenectomy and standard lymphadenectomy in EC and CC.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Indocyanine green-guided systematic pelvic lymphadenectomy

Study Design

Study Type:
Observational
Anticipated Enrollment :
100 participants
Observational Model:
Case-Control
Time Perspective:
Retrospective
Official Title:
Evaluation of Indocyanine Green-guided Systematic Pelvic Lymphadenectomy in Endometrial and Cervical Cancer
Anticipated Study Start Date :
Feb 1, 2025
Anticipated Primary Completion Date :
Feb 1, 2030
Anticipated Study Completion Date :
Feb 1, 2035

Arms and Interventions

Arm Intervention/Treatment
Indocyanine green

Women with endometrial and cervical cancer undergoing indocyanine green-guided systematic pelvic lymphadenectomy by laparoscopy or robotic surgery

Procedure: Indocyanine green-guided systematic pelvic lymphadenectomy
Injection of Indocyanine green within the uterine cervix before to perform laparoscopic/robotic systematic pelvic lymphadenectomy

Control

Women with endometrial and cervical cancer undergoing systematic pelvic lymphadenectomy by laparoscopy or robotic surgery without the use of indocyanine green tracer injection.

Outcome Measures

Primary Outcome Measures

  1. Retrieved lymph nodes [At the moment of the surgery]

    Number of retrieved lymph nodes after laparoscopic/robotic systematic pelvic lymphadenectomy

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 70 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Women affected by endometrial or cervical cancer

  • Laparoscopic/robotic surgical approach with systematic pelvic lymphadenectomy.

Exclusion Criteria:
  • Women undergoing open surgery (laparotomy) for the surgical management of endometrial or cervical cancer.

Contacts and Locations

Locations

No locations specified.

Sponsors and Collaborators

  • Università degli Studi dell'Insubria

Investigators

  • Principal Investigator: Benito Chiofalo, M.D., Regina Elena National Cancer Institute, Rome, Italy
  • Study Chair: Antonio Simone Laganà, M.D., Ph.D., Università degli Studi dell'Insubria

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Antonio Simone Laganà, Principal Investigator, Università degli Studi dell'Insubria
ClinicalTrials.gov Identifier:
NCT04246580
Other Study ID Numbers:
  • GREEN-1
First Posted:
Jan 29, 2020
Last Update Posted:
Apr 29, 2021
Last Verified:
Apr 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Antonio Simone Laganà, Principal Investigator, Università degli Studi dell'Insubria
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 29, 2021