DCVaccineMel: Vaccine Biotherapy of Cancer: Autologous Tumor Cells and Dendritic Cells

Sponsor
Hoag Memorial Hospital Presbyterian (Other)
Overall Status
Completed
CT.gov ID
NCT00948480
Collaborator
(none)
56
1
83
0.7

Study Details

Study Description

Brief Summary

This protocol was conducted as a single institution trial at Hoag Cancer Center, Hoag Hospital, Newport Beach, California. It was a single-arm phase II trial in which patients with metastatic melanoma received subcutaneous (s.c.) injections of irradiated autologous tumor cells that had been established as short-term cell lines, in conjunction with their own dendritic cells (DC) and granulocyte macrophage colony-stimulating factor [GM-CSF]. Eligible patients had regionally recurrent and/or distant metastatic cancer.

Condition or Disease Intervention/Treatment Phase
  • Biological: Autologous tumor cells plus dendritic cells
  • Drug: GM-CSF
Phase 2

Detailed Description

Patients were stratified by whether they had no measurable disease [NMD] at the time of treatment (usually because of surgical resection of metastases), or whether they had objectively measurable disease (OMD) by physical examination or radiologic scans per response evaluation criteria in solid tumors (RECIST criteria). Key endpoints were the results of delayed type hypersensitivity (DTH) skin testing to their own irradiated tumor cells, event-free survival [death or disease progression], overall survival, and objective tumor regression in patients who have measurable disease at the time vaccine therapy was initiated. This study was activated in the fall of 2000, and closed to accrual in June 2007.

Study Design

Study Type:
Interventional
Actual Enrollment :
56 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Vaccine Biotherapy Of Cancer: Autologous Tumor Cells and Dendritic Cells as Active Specific Immunotherapy in Patients With Metastatic Melanoma
Study Start Date :
Oct 1, 2000
Actual Primary Completion Date :
Sep 1, 2007
Actual Study Completion Date :
Sep 1, 2007

Outcome Measures

Primary Outcome Measures

  1. event-free survival [death or disease progression] [5.5 years after treatment initation]

Secondary Outcome Measures

  1. Overall survival [5.5 years after treatment initation]

Eligibility Criteria

Criteria

Ages Eligible for Study:
16 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Recurrent or metastatic melanoma as defined by stage IV disease (distant metastases), or any recurrent melanoma manifested by lymph node metastases or soft tissue nodules

  • ECOG Performance status of 0-2

  • Satisfactory medical condition for treatment in a phase I-II trial of anticancer therapy

  • Age > 16 years

  • Venous access for leukopheresis procedure to obtain peripheral blood lymphocytes to generate dendritic cells.

  • Serum pregnancy test must be negative for women of childbearing potential.

Exclusion Criteria:
  • Active central nervous system metastases

  • Known autoimmune disease or disease process that involves the use of immunosuppressive therapy.

  • Underlying cardiac disease associated with New York Heart Association class III or IV function, or unstable angina related to atherosclerotic cardiovascular disease.

  • Ongoing transfusion requirements, no significant hepatic or renal dysfunction, creatinine < 2.0 mg/dl, bilirubin < 2.0 mg/dl, albumin > 3.0 mg/dl, hematocrit > 25, platelets > 100,000.

  • Active infection or other active medical condition that could be eminently life threatening, including no active blood clotting or bleeding diathesis.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hoag Memorial Hospital Presbyterian Newport Beach California United States 92658

Sponsors and Collaborators

  • Hoag Memorial Hospital Presbyterian

Investigators

  • Principal Investigator: Robert O Dillman, MD, Hoag Memorial Hospital Presbyterian

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
, ,
ClinicalTrials.gov Identifier:
NCT00948480
Other Study ID Numbers:
  • DC Melanoma
First Posted:
Jul 29, 2009
Last Update Posted:
Jul 15, 2016
Last Verified:
Jul 1, 2016
Keywords provided by , ,
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 15, 2016