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Inducing Systemic Immunity and Regressions in Metastatic Melanoma

Primary Purpose

Metastatic Malignant Melanoma

Status
Completed
Phase
Phase 1
Locations
Study Type
Interventional
Intervention
Autologous cytokines
Sponsored by
NYU Langone Health
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Metastatic Malignant Melanoma

Eligibility Criteria

21 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Multiple cutaneous or subcutaneous metastases of melanoma

Exclusion Criteria:

  • Visceral metastases on admission.
  • No current chemotherapy or immunotherapy.
  • Note study performed between 1978 and 2002 before current therapies were available.

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    Autologous cytokiines

    Arm Description

    Autologous cytokines obtained from patients' blood mononuclear cells injected in volumes of 0.1 ml

    Outcomes

    Primary Outcome Measures

    Immune responses as evidenced by lymphocytic infiltrates in never-injected nodules.
    The biopsies were examined by a licensed pathologist for the presence of dense lymphocytic infiltrates.

    Secondary Outcome Measures

    Complete regression of a metastasis
    70 % of patients had at least one nodule regress. 40 % had all metastases completely regress for 5 to 20 years (median 60 months).

    Full Information

    First Posted
    January 14, 2015
    Last Updated
    January 26, 2015
    Sponsor
    NYU Langone Health
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    1. Study Identification

    Unique Protocol Identification Number
    NCT02350972
    Brief Title
    Inducing Systemic Immunity and Regressions in Metastatic Melanoma
    Official Title
    Inducing Systemic Immunity and Regressions in Metastatic Melanoma
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    January 2015
    Overall Recruitment Status
    Completed
    Study Start Date
    July 1978 (undefined)
    Primary Completion Date
    May 2002 (Actual)
    Study Completion Date
    May 2002 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    NYU Langone Health

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    In patients with multiple metastatic nodules of melanoma, the investigators evaluated whether autologous cytokines injected into cutaneous metastases would induce a systemic immune response as evidenced by the accumulation of dense lymphocytic infiltrates in metastases that had never been injected. Such immune responses were observed, and often the never-injected metastasis regressed completely. 20% of patients remained free of disease for greater than 5 years.
    Detailed Description
    Lymphocytic infiltrates were seen in never-injected nodules only after several weeks of injections elsewhere. No adverse events were seen. The tumor-infiltrating lymphocytes were able to kill autologous melanoma ex vivo. Some patients who experienced complete regressions of all metastases lived without disease for over 10 years.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Metastatic Malignant Melanoma

    7. Study Design

    Primary Purpose
    Basic Science
    Study Phase
    Phase 1
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    88 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    Autologous cytokiines
    Arm Type
    Experimental
    Arm Description
    Autologous cytokines obtained from patients' blood mononuclear cells injected in volumes of 0.1 ml
    Intervention Type
    Biological
    Intervention Name(s)
    Autologous cytokines
    Other Intervention Name(s)
    cytokine/chemokine
    Intervention Description
    Sterile autologous cytokines were injected weekly into multiple metastatic nodules while other nodules in the patient were never injected and were monitored for the development of dense lymphocytic infiltrates as evidence of an induced immune response.
    Primary Outcome Measure Information:
    Title
    Immune responses as evidenced by lymphocytic infiltrates in never-injected nodules.
    Description
    The biopsies were examined by a licensed pathologist for the presence of dense lymphocytic infiltrates.
    Time Frame
    Cutaneous nodules were biopsied by a surgeon afer 8 to 20 weeks of injections.
    Secondary Outcome Measure Information:
    Title
    Complete regression of a metastasis
    Description
    70 % of patients had at least one nodule regress. 40 % had all metastases completely regress for 5 to 20 years (median 60 months).
    Time Frame
    Complete regressions of all injected and never-injected metastases occurred in different pts after 13 weeks to 48 months of injections. Pts with progressive disease were switched to chemotherapy at any point in the study.

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    21 Years
    Maximum Age & Unit of Time
    80 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Multiple cutaneous or subcutaneous metastases of melanoma Exclusion Criteria: Visceral metastases on admission. No current chemotherapy or immunotherapy. Note study performed between 1978 and 2002 before current therapies were available.
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Fred T. Valentine, M.D.
    Organizational Affiliation
    NYU Langone Health
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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    Inducing Systemic Immunity and Regressions in Metastatic Melanoma

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