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Transfected Dendritic Cell Based Therapy for Patients With Breast Cancer or Malignant Melanoma

Primary Purpose

Breast Cancer, Malignant Melanoma

Status
Completed
Phase
Phase 1
Locations
Denmark
Study Type
Interventional
Intervention
DC vaccine
Sponsored by
Inge Marie Svane
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Breast Cancer focused on measuring dendritic cell, cancervaccine, breast cancer, malignant melanoma, Cyclophosphamide

Eligibility Criteria

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

Inclusion Criteria:

  1. Histological verified metastatic breast cancer or malignant melanoma, in progression
  2. ≥ 18 years
  3. the patient must be habil
  4. Performance status ≤ 1 on Zubrod-ECOG-WHO-scale
  5. Leukocytes and platelets must be ≥normal. Hg ≥ 6.0
  6. creatinin must be normal
  7. Liverparametre <2.5 x normal. Bilirubin <30
  8. Expected survival > 3 months
  9. Informed consent

11. At least one measurable lesion according to RECIST criteria.

Exclusion Criteria:

  1. Indication for chemotherapy
  2. Other malignancies
  3. Brain metastases
  4. severe medical condition
  5. Acute/chronic infection with ex. HIV, hepatitis, tuberculose
  6. Severe allergy
  7. Autoimmune disease
  8. Other treatment with immune suppressing agents, other anticancer agents or experimental drugs
  9. Uncontrolled hypercalcemia.

Sites / Locations

  • Department of Oncology, Herlev University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

DC vaccination and Cyclophosphamide

Arm Description

Outcomes

Primary Outcome Measures

to evaluate the toxicity of the vaccine in combination with Cyclophosphamide

Secondary Outcome Measures

to investigate the clinical tumor response and the duration
to evaluate the duration of tumor and immunoresponse
to evaluate immune response

Full Information

First Posted
September 16, 2009
Last Updated
August 18, 2015
Sponsor
Inge Marie Svane
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1. Study Identification

Unique Protocol Identification Number
NCT00978913
Brief Title
Transfected Dendritic Cell Based Therapy for Patients With Breast Cancer or Malignant Melanoma
Official Title
Evaluation of Dendritic Cells Transfected With Survivin, hTERT and p53 mRNA as a Treatment for Patients With Metastatic Breast Cancer or Malignant Melanoma
Study Type
Interventional

2. Study Status

Record Verification Date
August 2015
Overall Recruitment Status
Completed
Study Start Date
September 2009 (undefined)
Primary Completion Date
August 2013 (Actual)
Study Completion Date
May 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Inge Marie Svane

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The primary aim of this study is to evaluate the toxicity of the vaccine and the combination of the vaccine and Cyclophosphamide, and to evaluate the immune response induced by the vaccine. The secondary aim is to investigate the clinical tumour response and duration of tumour and immune response.
Detailed Description
Phase I trial. Single center study; patients will be referred to the study center from other institutions in Denmark. 14 patients will be included in this phase I trial DC vaccination regime consists of primary 6 biweekly intradermal injections with transfected dendritic cells, followed by monthly injections until progression; Cyclophosphamide is used as vaccine adjuvant. Defined procedures are employed for generation of autologous dendritic cells for clinical application in a classified laboratory. Unmobilized leukapheresis will be used for isolation of large-scale mononuclear cells, and dendritic cells will be generated from monocytes by cytokine stimulation and transfected with mRNA encoding for hTERT, survivin and p53 if the tumour express p53. Frozen preparations of dendritic cells will be prepared using automated cryopreservation. Each patient will receive a minimum of 1x106 dendritic cells per treatment supplemented with Cyclophosphamide 50 mg twice a day every second week. Toxicity including autoimmunity will be evaluated using the Common Toxicity Criteria (CTC).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Breast Cancer, Malignant Melanoma
Keywords
dendritic cell, cancervaccine, breast cancer, malignant melanoma, Cyclophosphamide

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
DC vaccination and Cyclophosphamide
Arm Type
Experimental
Intervention Type
Biological
Intervention Name(s)
DC vaccine
Other Intervention Name(s)
dendritic cell vaccine, Cyclophosphamide, Sendoxan®, Baxter
Intervention Description
DC vaccination, one vaccine biweekly
Primary Outcome Measure Information:
Title
to evaluate the toxicity of the vaccine in combination with Cyclophosphamide
Time Frame
biweekly
Secondary Outcome Measure Information:
Title
to investigate the clinical tumor response and the duration
Time Frame
after 12 weeks
Title
to evaluate the duration of tumor and immunoresponse
Time Frame
3, 6, 9 months
Title
to evaluate immune response
Time Frame
at 8 and 12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histological verified metastatic breast cancer or malignant melanoma, in progression ≥ 18 years the patient must be habil Performance status ≤ 1 on Zubrod-ECOG-WHO-scale Leukocytes and platelets must be ≥normal. Hg ≥ 6.0 creatinin must be normal Liverparametre <2.5 x normal. Bilirubin <30 Expected survival > 3 months Informed consent 11. At least one measurable lesion according to RECIST criteria. Exclusion Criteria: Indication for chemotherapy Other malignancies Brain metastases severe medical condition Acute/chronic infection with ex. HIV, hepatitis, tuberculose Severe allergy Autoimmune disease Other treatment with immune suppressing agents, other anticancer agents or experimental drugs Uncontrolled hypercalcemia.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Inge Marie Svane, prof.MD
Organizational Affiliation
Department of Oncology, Herlev University Hospital, Herlev Ringvej 75,2730 Herlev
Official's Role
Study Director
Facility Information:
Facility Name
Department of Oncology, Herlev University Hospital
City
Herlev
ZIP/Postal Code
Dk 2730
Country
Denmark

12. IPD Sharing Statement

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Transfected Dendritic Cell Based Therapy for Patients With Breast Cancer or Malignant Melanoma

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