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Tilmanocept vs Sulfur Colloid in Sentinel Lymph Node Biopsy

Primary Purpose

Sentinel Lymph Node Biopsy, Breast Cancer

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Tc 99m tilmanocept
Tc 99m filtered sulfur colloid
Sponsored by
Memorial Health University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Sentinel Lymph Node Biopsy

Eligibility Criteria

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

Inclusion Criteria:

  • Women above 18 years of age with biopsy proven, clinically stage 1 or 2 breast cancer who will be undergoing partial mastectomy with SLNBx at Memorial Health

Exclusion Criteria:

  • Women under the age of 18,
  • Clinically positive axillary nodes
  • Neoadjuvant therapy for current breast cancer diagnosis
  • Women with previous SLNBx or axillary node dissection
  • Pregnant women
  • Women with previous radiation above the diaphragm, and below the neck

Sites / Locations

  • Memorial Health University Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Tilmanocept

Sulfur Colloid

Arm Description

Tc 99m tilmanocept

Tc 99m filtered sulfur colloid

Outcomes

Primary Outcome Measures

Number of harvested lymph nodes
Looking for differences between the treatment arms in the number of harvest sentinel lymph nodes

Secondary Outcome Measures

Full Information

First Posted
June 23, 2017
Last Updated
August 23, 2018
Sponsor
Memorial Health University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT03199560
Brief Title
Tilmanocept vs Sulfur Colloid in Sentinel Lymph Node Biopsy
Official Title
A Randomized Controlled Double-blinded Study Comparing the Intraoperative Injection of Lymphatic Mapping Agents Tc 99m Tilmanocept to Tc 99m Filtered Sulfur Colloid in Breast Cancer Patients Undergoing Breast Conservation and Sentinel Lymph Node Biopsy
Study Type
Interventional

2. Study Status

Record Verification Date
August 2018
Overall Recruitment Status
Unknown status
Study Start Date
June 22, 2017 (Actual)
Primary Completion Date
June 22, 2019 (Anticipated)
Study Completion Date
August 22, 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Memorial Health University Medical Center

4. Oversight

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

5. Study Description

Brief Summary
A randomized controlled double-blinded study comparing the intraoperative injection of lymphatic mapping agents Tc 99m tilmanocept to Tc 99m filtered sulfur colloid in breast cancer patients undergoing breast conservation and sentinel lymph node biopsy
Detailed Description
This study is a double-blinded randomized control trial comparing tilmanocept to TSC as intraoperative radiolabeled mapping agents in female patients with early stage breast cancer undergoing partial mastectomy with SLNBx. To secure this aim, patients who are schedule to undergo partial mastectomy and SLBx will be consented and randomized (randomization table) into one of two experimental arms, tilmanocept or TSC. These patients will then undergo their scheduled partial mastectomy with SLNBx, with the patient and surgeon blinded to the randomization result. The respective radiotracers will both be delivered to the OR in the same delivery device and volumes to continue to preserve anonymity of the material. Care will be taken to handle the radiotracers along the standards and guidelines that are already in practice in Memorial Health University Hospital's nuclear medicine department. Two intradermal injections of these radiotracers will be delivered at 3 and 6 o'clock positions at the edge of the areola, after induction of general anesthesia, allowing for less discomfort to the patient. Methylene blue (5-10 ml) will also be injected in the subareolar space immediately afterwards in all study patients, using a separate syringe, in accordance with the surgeon's current standard practice. Transcutaneous probing of the axilla measuring counts per second will be performed in 3 minute intervals after injection of the radiotracer. Incision in the axilla can, at the earliest, be at 15 minutes, as this is the FDA approved earliest time for tilmanocept. At this time, if the transcutaneous "hot spot" detected by the gamma detector probe is detected, an incision for SLNBx will proceed. A hot spot is defined as an area of increased radioactivity in the axilla with a fall-off in radioactive counts in adjacent tissue. If a hot spot is not detected, transcutaneous probing will continue at 3 minute intervals until this value is reached. In an effort to not prolong the anesthesia time, incision at 30 minutes will be performed even if a hot spot is not identified transcutaneously. No changes will be made to the method of SLNBx for this study. As axillary lymph node dissection is no longer the standard of care at the time of SLNBx in partial mastectomy, we will continue the practice of sending the SLN for permanent sectioning, however this will be at the surgeon's discretion. If at the time of surgery there are histologically metastatic nodes or if a sentinel node cannot be identified, the surgeon can proceed to axillary lymph node dissection at their discretion, however for the purposes of this study only SLN data will be tracked (please see below for further information on data collection). Description of method for SLNBx: After the intradermal injection of tilmanocept or TSC and sub-areolar injection of methylene blue, and the decision to proceed with SLNBx, the standard incision will be made in the axilla overlying the area with the most counts per second per the gamma probe. The subcutaneous tissues are then dissected to the clavipectoral fascia. The fascia is then incised and the axilla is again probed with the gamma probe. Once a blue node or radioactive node(s) is detected they are excised. A radioactive node will be defined as having counts per second that are 10 times higher than surrounding tissue (background count). Once excised, an "ex-vivo" count will be taken of the sentinel node(s) and recorded. If the background radiation of the axilla is less than 10% the counts per second (cps) of the "hottest" harvested sentinel lymph node, the search for radioactive sentinel nodes will be deemed complete. If there is greater than 10% the counts per second remaining in the axilla, then additional nodes will be identified and excised using the same methods until the background radiation is less than 10% the counts per second of the hottest sentinel nodes removed. Additional nodes which are blue but not radioactive will be excised, as will any clinically suspicious nodes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Sentinel Lymph Node Biopsy, Breast Cancer

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
double-blinded randomized control trial
Masking
ParticipantCare ProviderInvestigator
Masking Description
A double-blind study. Study compound will be masked before dispensing to care team.
Allocation
Randomized
Enrollment
86 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Tilmanocept
Arm Type
Active Comparator
Arm Description
Tc 99m tilmanocept
Arm Title
Sulfur Colloid
Arm Type
Active Comparator
Arm Description
Tc 99m filtered sulfur colloid
Intervention Type
Drug
Intervention Name(s)
Tc 99m tilmanocept
Other Intervention Name(s)
LymphoSeek
Intervention Description
lymphatic mapping agent
Intervention Type
Drug
Intervention Name(s)
Tc 99m filtered sulfur colloid
Intervention Description
lymphatic mapping agent
Primary Outcome Measure Information:
Title
Number of harvested lymph nodes
Description
Looking for differences between the treatment arms in the number of harvest sentinel lymph nodes
Time Frame
1 day

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Women above 18 years of age with biopsy proven, clinically stage 1 or 2 breast cancer who will be undergoing partial mastectomy with SLNBx at Memorial Health Exclusion Criteria: Women under the age of 18, Clinically positive axillary nodes Neoadjuvant therapy for current breast cancer diagnosis Women with previous SLNBx or axillary node dissection Pregnant women Women with previous radiation above the diaphragm, and below the neck
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
William Burak, MD
Phone
9123502700
Email
CoreySa1@memorialhealth.com
First Name & Middle Initial & Last Name or Official Title & Degree
Samuel Corey, MD
Phone
9123502700
Email
CoreySa1@memorialhealth.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
William Burak, MD
Organizational Affiliation
Memorial Health University Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Memorial Health University Medical Center
City
Savannah
State/Province
Georgia
ZIP/Postal Code
31404
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
William Burak, MD
Phone
912-350-2700
Email
CoreySa1@memorialhealth.com

12. IPD Sharing Statement

Plan to Share IPD
No

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Tilmanocept vs Sulfur Colloid in Sentinel Lymph Node Biopsy

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