Mapping Draining Lymph Nodes in CNS Malignancies

Sponsor
Washington University School of Medicine (Other)
Overall Status
Recruiting
CT.gov ID
NCT04096716
Collaborator
Lloyd J. Old STAR Program (Other)
30
1
6
48.9
0.6

Study Details

Study Description

Brief Summary

The purpose of this research study is to determine whether the lymph nodes that drain a brain tumor can be detected by imaging after injection of a substance called Tc-99m tilmanocept directly into the brain tissue around the tumor. Tc-99m tilmanocept is a radioactive substance that is used to find lymph nodes by injecting it and then scanning the body with a device that can trace its radioactivity. In this study, the investigators are looking to see how long it takes the Tc-99m tilmanocept to travel from the tumor to the lymph nodes. The investigators will be using it to map lymph nodes as they relate to specific brain areas.

Condition or Disease Intervention/Treatment Phase
  • Drug: Tc-99m tilmanocept
Phase 1

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Mapping Draining Lymph Nodes in CNS Malignancies
Actual Study Start Date :
Dec 3, 2019
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
Experimental: Cohort 1: Tc-99m tilmanocept

The surgeon will inject up to 0.5 mL of reconstituted Tc-99m tilmanocept using a blunt tipped needle 1 cm into the wall of the resection cavity after completing surgical resection of the tumor Portable planar imaging will be obtained at 4.5 ± 2.5 hours and 24 +/- 8 hours after injection of Tc-99m tilmanocept.

Drug: Tc-99m tilmanocept
Tc-99m tilmanocept is a radioactive diagnostic agent.
Other Names:
  • Lymphoseek
  • Experimental: Cohort 2A: Tc-99m tilmanocept frontal lobe injection site

    The surgeon will inject up to 0.5 mL of reconstituted Tc-99m tilmanocept using a blunt tipped needle 1 cm into the wall of the resection cavity after completing surgical resection of the tumor SPECT/CT of the head and neck will be obtained when practical on the day of surgery. If the patient is not sufficiently recovered from surgery to be transported to the Division of Nuclear Medicine for imaging, SPECT/CT will be done on Day 2

    Drug: Tc-99m tilmanocept
    Tc-99m tilmanocept is a radioactive diagnostic agent.
    Other Names:
  • Lymphoseek
  • Experimental: Cohort 2B: Tc-99m tilmanocept parietal lobe injection site

    The surgeon will inject up to 0.5 mL of reconstituted Tc-99m tilmanocept using a blunt tipped needle 1 cm into the wall of the resection cavity after completing surgical resection of the tumor SPECT/CT of the head and neck will be obtained when practical on the day of surgery. If the patient is not sufficiently recovered from surgery to be transported to the Division of Nuclear Medicine for imaging, SPECT/CT will be done on Day 2

    Drug: Tc-99m tilmanocept
    Tc-99m tilmanocept is a radioactive diagnostic agent.
    Other Names:
  • Lymphoseek
  • Experimental: Cohort 2C: Tc-99m tilmanocept temporal lobe injection site

    The surgeon will inject up to 0.5 mL of reconstituted Tc-99m tilmanocept using a blunt tipped needle 1 cm into the wall of the resection cavity after completing surgical resection of the tumor SPECT/CT of the head and neck will be obtained when practical on the day of surgery. If the patient is not sufficiently recovered from surgery to be transported to the Division of Nuclear Medicine for imaging, SPECT/CT will be done on Day 2

    Drug: Tc-99m tilmanocept
    Tc-99m tilmanocept is a radioactive diagnostic agent.
    Other Names:
  • Lymphoseek
  • Experimental: Cohort 2D: Tc-99m tilmanocept occipital lobe injection site

    The surgeon will inject up to 0.5 mL of reconstituted Tc-99m tilmanocept using a blunt tipped needle 1 cm into the wall of the resection cavity after completing surgical resection of the tumor SPECT/CT of the head and neck will be obtained when practical on the day of surgery. If the patient is not sufficiently recovered from surgery to be transported to the Division of Nuclear Medicine for imaging, SPECT/CT will be done on Day 2

    Drug: Tc-99m tilmanocept
    Tc-99m tilmanocept is a radioactive diagnostic agent.
    Other Names:
  • Lymphoseek
  • Experimental: Cohort 3: Tc-99m tilmanocept stereotactic needle biopsy of tumor

    The surgeon will inject up to 0.3 mL of reconstituted Tc-99m tilmanocept after completing the stereotactic biopsy of the tumor SPECT/CT of the head and neck will be obtained on the day of biopsy, when practical. If the patient is not sufficiently recovered from biopsy to be transported to the Division of Nuclear Medicine for imaging, SPECT/CT will be done on Day 2

    Drug: Tc-99m tilmanocept
    Tc-99m tilmanocept is a radioactive diagnostic agent.
    Other Names:
  • Lymphoseek
  • Outcome Measures

    Primary Outcome Measures

    1. Time course of Tc-99m tilmanocept drainage to the lymph nodes from the brain (Cohort 1 only) [Up to Day 2]

    2. Identify and map lymph nodes from distinct brain regions as measured by the 2013 international consensus guidelines for cervical and cranial lymph nodes [Up to Day 2]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Candidate for surgical resection or stereotactic biopsy of suspected brain tumor, including benign tumors (e.g., meningioma) and malignant tumors (e.g., glioma or metastatic disease).

    • Suitable candidate to receive Tc-99m tilmanocept injection and study related imaging post-operatively per the Principal Investigator and/or treating neurosurgeon.

    • At least 18 years of age.

    • Willing and able to provide informed consent (or consent of legally authorized representative).

    Exclusion Criteria:
    • Documented hypersensitivity to dextran and/or modified forms of dextran.

    • Pregnant.

    • Prior surgical evacuation of lymph nodes of the head and/or neck

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Washington University School of Medicine Saint Louis Missouri United States 63110

    Sponsors and Collaborators

    • Washington University School of Medicine
    • Lloyd J. Old STAR Program

    Investigators

    • Principal Investigator: Tanner Johanns, M.D., Ph.D., Washington University School of Medicine

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    None provided.
    Responsible Party:
    Washington University School of Medicine
    ClinicalTrials.gov Identifier:
    NCT04096716
    Other Study ID Numbers:
    • 201908018
    First Posted:
    Sep 20, 2019
    Last Update Posted:
    Feb 14, 2022
    Last Verified:
    Jan 1, 2022
    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
    Product Manufactured in and Exported from the U.S.:
    No
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Feb 14, 2022