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Detection of SLN in Patients With Endometrial Cancer Undergoing Robotic Assisted Staging: Comparison of ISB and ICG

Primary Purpose

Endometrial Cancer

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
ISB dye and standard white light imaging
ICG dye and FireFly fluorescence imaging
Sponsored by
AdventHealth
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Endometrial Cancer focused on measuring Sentinel lymph nodes, da Vinci, Firefly, Sentinel lymph node mapping, Fluorescence Imaging, SLN, SLN mapping

Eligibility Criteria

18 Years - 85 Years (Adult, Older Adult)FemaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. The patient must be ≥18 and ≤85 years of age.
  2. The patient must be female.
  3. The patient must be willing and able to provide informed consent.
  4. The patient is willing and able to comply with the study protocol.
  5. The patient has endometrial cancer and is scheduled for robotic hysterectomy and lymphadenectomy.
  6. The patient agrees to follow-up examinations out to 6-weeks post-treatment

Exclusion Criteria:

  1. The patient is not a candidate for robotic assisted hysterectomy and lymphadenectomy.
  2. The patient has known or suspected allergies to iodine, ICG or ISB.
  3. The patient has hepatic dysfunction confirmed by elevated liver function studies (i.e., hepatic enzyme SGOT, SGPT or Bilirubin > 2 x normal (based on reference values from the laboratory used by the patient)

Sites / Locations

  • Florida Hospital Gynecologic Oncology

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

ISB dye, standard white light

ICG dye, FireFly fluorescence imaging

Arm Description

SLN mapping utilizing da Vinci surgical system with Isosulfan Blue (ISB) dye and standard white light imaging.

SLN mapping utilizing da Vinci surgical system with ISB dye and standard white light first, and then additionally, Indocyanine Green (ICG) dye and FireFly fluorescence imaging.

Outcomes

Primary Outcome Measures

Number of Pelvic Sentinel Lymph Nodes (SLN) in Endometrial Cancer Patients Detected by Either ICG and/or ISB Dyes.

Secondary Outcome Measures

Negative Predictive Value (NPV) of Pelvic SLN in Endometrial Cancer in Relation to the Number of Nodes With Metastasis.
The standard definition for negative predictive value was used to calculate NPV. There was one false negative SLN in this study, 39 true positive sentinel lymph nodes, and 140 negative pelvic metastatic patients. NPV = 140/141=99.3%

Full Information

First Posted
February 14, 2014
Last Updated
August 20, 2019
Sponsor
AdventHealth
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1. Study Identification

Unique Protocol Identification Number
NCT02068820
Brief Title
Detection of SLN in Patients With Endometrial Cancer Undergoing Robotic Assisted Staging: Comparison of ISB and ICG
Official Title
Detection of Sentinel Lymph Nodes in Patients With Endometrial Cancer Undergoing Robotic-Assisted Staging: Comparison of Isosulfan Blue (ISB) and Indocyanine Green Dyes (ICG) With Fluorescence Imaging
Study Type
Interventional

2. Study Status

Record Verification Date
August 2019
Overall Recruitment Status
Completed
Study Start Date
September 2012 (undefined)
Primary Completion Date
January 2015 (Actual)
Study Completion Date
January 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
AdventHealth

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The investigators hypothesis is that if sensitivity and specificity are found to be significantly higher than the current reports with Technesium-99 and ISB colorimetric dye, SLN biopsies might allow omission of full lymphadenectomy in lower-risk cases, thereby limiting peri-operative morbidity. SLN biopsies might also improve the detection of metastatic disease, essentially lowering the recognized false-negative rate of standard lymphadenectomy analyzed by routine H&E pathologic analysis.
Detailed Description
The study objective is to compare two sentinel lymph node detection technologies [fluorescence imaging and Indocyanine Green (ICG) dye verses standard laparoscopic colorimetric analysis using Isosulfan Blue (ISB) dye] for sensitivity and specificity of detecting metastatic disease in pelvic lymph nodes of women with endometrial cancer undergoing robotic-assisted laparoscopic hysterectomy and lymphadenectomy. The following three specific aims would be addressed in this research proposal: Specific Aim 1: To determine the ability of mapping bilaterally pelvic SLN in women with endometrial cancer undergoing robotic-assisted laparoscopic staging comparing two different methods (i.e., comparing the combination of colorimetric analysis-ISB dye + fluorescence imaging-ICG dye vs. colorimetric analysis-ISB dye alone). Specific Aim 2: To estimate the negative predictive value (NPV) of pelvic SLN in endometrial cancer with respect to predicting nodal metastasis. Specific Aim 3: To evaluate the ability of sentinel lymph nodes to increase the detection of metastatic disease through ultra-sectioning and immuno-histochemical (IHC) staining by comparing IHC results and standard hematoxylin and eosin (H&E) results.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Endometrial Cancer
Keywords
Sentinel lymph nodes, da Vinci, Firefly, Sentinel lymph node mapping, Fluorescence Imaging, SLN, SLN mapping

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
200 (Actual)

8. Arms, Groups, and Interventions

Arm Title
ISB dye, standard white light
Arm Type
Active Comparator
Arm Description
SLN mapping utilizing da Vinci surgical system with Isosulfan Blue (ISB) dye and standard white light imaging.
Arm Title
ICG dye, FireFly fluorescence imaging
Arm Type
Experimental
Arm Description
SLN mapping utilizing da Vinci surgical system with ISB dye and standard white light first, and then additionally, Indocyanine Green (ICG) dye and FireFly fluorescence imaging.
Intervention Type
Device
Intervention Name(s)
ISB dye and standard white light imaging
Other Intervention Name(s)
Isosulfan Blue dye
Intervention Description
Sentinel lymph node mapping utilizing the da Vinci surgical system and ISB dye with standard white light imaging.
Intervention Type
Device
Intervention Name(s)
ICG dye and FireFly fluorescence imaging
Other Intervention Name(s)
Indocyanine green dye
Intervention Description
Sentinel lymph node mapping utilizing the da Vinci surgical system with ICG dye and FireFly fluorescence imaging.
Primary Outcome Measure Information:
Title
Number of Pelvic Sentinel Lymph Nodes (SLN) in Endometrial Cancer Patients Detected by Either ICG and/or ISB Dyes.
Time Frame
through 6 weeks post-operative
Secondary Outcome Measure Information:
Title
Negative Predictive Value (NPV) of Pelvic SLN in Endometrial Cancer in Relation to the Number of Nodes With Metastasis.
Description
The standard definition for negative predictive value was used to calculate NPV. There was one false negative SLN in this study, 39 true positive sentinel lymph nodes, and 140 negative pelvic metastatic patients. NPV = 140/141=99.3%
Time Frame
through 6 weeks post-operative
Other Pre-specified Outcome Measures:
Title
Number of Pelvic Sentinal Lymph Nodal Metastasis in Regard to Staining by Immunohistochemical (IHC) Staining in Comparison to Standard Hematoxylin and Eosin (H&E).
Description
Of the 127 positive nodes with pathology information, the percentage of each type of node will be summarized by the staining method. Statistical testing of the individual staining methods compared to both will be computed using Chi-square test of independence.
Time Frame
through 6 weeks post-operative

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: The patient must be ≥18 and ≤85 years of age. The patient must be female. The patient must be willing and able to provide informed consent. The patient is willing and able to comply with the study protocol. The patient has endometrial cancer and is scheduled for robotic hysterectomy and lymphadenectomy. The patient agrees to follow-up examinations out to 6-weeks post-treatment Exclusion Criteria: The patient is not a candidate for robotic assisted hysterectomy and lymphadenectomy. The patient has known or suspected allergies to iodine, ICG or ISB. The patient has hepatic dysfunction confirmed by elevated liver function studies (i.e., hepatic enzyme SGOT, SGPT or Bilirubin > 2 x normal (based on reference values from the laboratory used by the patient)
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Robert Holloway, MD
Organizational Affiliation
Florida Hospital Gynecologic Oncology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Florida Hospital Gynecologic Oncology
City
Orlando
State/Province
Florida
ZIP/Postal Code
32804
Country
United States

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Detection of SLN in Patients With Endometrial Cancer Undergoing Robotic Assisted Staging: Comparison of ISB and ICG

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