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
About this trial
This is an interventional basic science trial for Metastatic Malignant Melanoma
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.
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
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
Learn more about this trial
Inducing Systemic Immunity and Regressions in Metastatic Melanoma
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