SLN Mapping and ICG Dye for Vulvar Cancer

Sponsor
Tufts Medical Center (Other)
Overall Status
Not yet recruiting
CT.gov ID
NCT06035068
Collaborator
(none)
10
1
18
0.6

Study Details

Study Description

Brief Summary

Doctors typically use blue dye to assist in locating and extracting lymph nodes for biopsy. However, this process can prove somewhat challenging for both patients and medical teams due to its need for extensive coordination and the assistance of a nuclear medicine team. Some studies have talked about using a different method to find these lymph nodes using a special dye called Indocyanine Green (ICG). This method involves shining a special camera on the skin. So far, no studies have directly compared the ICG method to the standard blue dye. The ICG camera could make things easier for patients and doctors, and more patients might choose to have their lymph nodes checked with this new method. The goal of our study is to see if using the ICG dye is just as good as the standard method of blue dye.

Condition or Disease Intervention/Treatment Phase
  • Drug: Indocyanine green

Study Design

Study Type:
Observational
Anticipated Enrollment :
10 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Sentinel Lymph Node Mapping and Detection With Indocyanine Green and Spy-Phi Handheld Camera Technology in Early-Stage Vulvar Cancer (PILOT)
Anticipated Study Start Date :
Dec 1, 2023
Anticipated Primary Completion Date :
Dec 1, 2024
Anticipated Study Completion Date :
Jun 1, 2025

Arms and Interventions

Arm Intervention/Treatment
Combined ICG dye and blue tracer dye

This study is being done to see if a different way of finding and removing lymph nodes during surgery, using a special camera and a dye called Indocyanine Green (ICG), works as well as the usual method with blue dye plus a radioactive tracer called radiocolloid. By comparing the two ways directly, we hope to make it simpler for people with vulvar cancer to get their lymph nodes checked during surgery.

Drug: Indocyanine green
Indocyanine green (ICG) is a fluorescent dye that has been used for the imaging of cancers in the body for more than 30 years.
Other Names:
  • ICG dye
  • Outcome Measures

    Primary Outcome Measures

    1. Detection Rate of SLNs using ICG Dye vs Blue Dye at Patient Level [Data collection at time of surgery]

      Report the detection rate of SLNs using ICG dye for sentinel lymph node mapping. Report the detection rate of SLNs using blue dye for sentinel lymph node mapping. Compare the two detection rates using a chi-squared test or Fisher's exact test, depending on the sample size.

    2. Clustered Analysis at the Hemi-Pelvis Level [Data collection at time of surgery]

      Use generalized estimating equations (GEE) or mixed-effects logistic regression models to account for the clustering effect. Include a random effect for each patient to address the correlation between SLNs within the same patient's hemi-pelvis. Assess the significance of dye type using the Wald test or likelihood ratio test. Report odds ratios, confidence intervals, and p-values for the effect of dye type on SLN detection.

    3. 3. Difference in SLNs Detected in Blue vs Green Dye when Data is Clustered at Hemi-Pelvis Level [Data collection at time of surgery]

      Report the proportion of SLNs detected using blue dye in each hemi-pelvis. Report the proportion of SLNs detected using ICG dye in each hemi-pelvis. Use a paired t-test or Mcnemar's test to compare the proportions within each hemi-pelvis. Account for the clustering effect by using mixed-effects models

    Secondary Outcome Measures

    1. Sensitivity, Specificity, and Negative Predictive Value of ICG Dye vs Standard Blue Dye [Data collection at time of surgery]

      Create a 2x2 contingency table for sensitivity, specificity, and negative predictive value. Sensitivity = (True Positives) / (True Positives + False Negatives). Specificity = (True Negatives) / (True Negatives + False Positives). Negative Predictive Value = (True Negatives) / (True Negatives + False Negatives).

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    Female
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • 18 years of age or older

    • Patients with early-stage SCC (diameter <4 cm) of the vulva without suspicious lymph nodes at palpation or imaging who are planned for surgery at Tufts Medical Center.

    • Patients with squamous cell carcinoma, depth of invasion > 1mm

    • Patients with T1 or T2 tumors (FIGO staging) < 4 cm, not encroaching in urethra or anus with clinically negative inguinofemoral lymph nodes

    • Localization and size of the tumor are such that perilesional injection of the tracers at three or four sites is possible

    • Preoperative imaging do not show enlarged (<1.5 cm)/ suspicious nodes

    • Willing and able to give informed consent

    Exclusion Criteria:
    • Inoperable tumors and tumors with diameter > 4 cm

    • Patients with inguinofemoral lymph nodes that are palpable on clinical exam suspicious for metastases or with cytologically proven inguinofemoral lymph node metastases

    • Radiologically enlarged (>1.5 cm) inguinofemoral lymph nodes

    • Patients with multifocal tumors

    • Pregnancy

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Tufts Medical Center Boston Massachusetts United States 02111

    Sponsors and Collaborators

    • Tufts Medical Center

    Investigators

    • Principal Investigator: Rafael Gonzalez, MD, Tufts Medical Center

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    Responsible Party:
    Tufts Medical Center
    ClinicalTrials.gov Identifier:
    NCT06035068
    Other Study ID Numbers:
    • STUDY00004163
    First Posted:
    Sep 13, 2023
    Last Update Posted:
    Sep 13, 2023
    Last Verified:
    Sep 1, 2023
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Sep 13, 2023