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Randomized Trial With Dendritic Cells in Patients With Metastatic Colorectal Cancer

Primary Purpose

Colorectal Neoplasms

Status
Completed
Phase
Phase 2
Locations
Spain
Study Type
Interventional
Intervention
Dendritic Cell Vaccine
Supportive treatment
Sponsored by
Fundacion Clinic per a la Recerca Biomédica
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Neoplasms focused on measuring Colorectal Neoplasms, Dendritic Cells

Eligibility Criteria

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

Inclusion Criteria:

  • Age over 18 years.
  • Capacity of understanding and signing the informed consent and to undergo the study procedures.
  • Previously treated with 2 lines of chemotherapy.
  • ECOG <= 2.
  • Adequate renal, hepatic and bone marrow function
  • Confirmed diagnosis of colorectal cancer with hepatic metastasis, suitable for biopsy.
  • Availability of tumor tissue, for maturing dendritic cells
  • RECIST.1 criteria

Exclusion Criteria:

  • Clinically relevant diseases or infections (HBV, HCV, HIV).
  • Pregnant or breast feeding women.
  • Immunosuppressant treatment.
  • Concurrent cancer, with the exceptions allowed by the principal investigator (PI).

Sites / Locations

  • Hospital Clínic Barcelona

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Other

Arm Label

Dendritic Cells Vaccine

Supportive treatment

Arm Description

Dendritic Cells Vaccine after 2 lines of chemotherapy

Supportive treatment after 2 lines of chemotherapy

Outcomes

Primary Outcome Measures

Progression Free Survival

Secondary Outcome Measures

Overall Survival

Full Information

First Posted
August 9, 2011
Last Updated
November 3, 2014
Sponsor
Fundacion Clinic per a la Recerca Biomédica
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1. Study Identification

Unique Protocol Identification Number
NCT01413295
Brief Title
Randomized Trial With Dendritic Cells in Patients With Metastatic Colorectal Cancer
Official Title
Randomized Phase II Trial in Patients With Progressive Stage IV Colorectal Cancer to Two Lines of Chemotherapy, in Order to Compare the Best Supportive Treatment Versus Treatment With Dendritic Cells Plus the Best Supportive Treatment
Study Type
Interventional

2. Study Status

Record Verification Date
November 2014
Overall Recruitment Status
Completed
Study Start Date
August 2011 (undefined)
Primary Completion Date
September 2014 (Actual)
Study Completion Date
September 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Fundacion Clinic per a la Recerca Biomédica

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The different alternatives used since 1996 to treat metastatic colorectal cancer (MCRC) have increased the mean survival of these patients. This outstanding advance is due to the extended indications for resection of hepatic metastases and to the use of new chemotherapeutic drugs (fluoropyrimidine, irinotecan and oxaliplatin) and monoclonal antibodies (bevacizumab, cetuximab and panitumumab). However, none of these treatments is curative and the majority of patients are overwhelmed by the illness. The first line of treatment for MCRC is FOLFOX and the second, irinotecan plus cetuximab for patients with wild type KRAS gene (60%) with a 30% responses, and bevacizumab plus irinotecan with a 5-10% of responses, in patients with mutated KRAS (40%). A treatment with autologous dendritic cells (DCs) pulsed with autologous tumour antigens is proposed as a third line of therapy. A randomized phase II trial would be performed, by selecting two groups of patients, one of them would be treated with the best supportive treatment and the other with DCs plus the best supportive treatment. The aim of the study would be to analyze the outcome after 4 months of treatment. In patients treated with DCs, IFN-γ spot forming cells and proliferative responses would be determined pre and post treatment in lymphocytes stimulated with autologous DCs pulsed with autologous tumour antigens. Pre and post treatment serum levels of IFN-γ, TNF-α, TGF-β e IL-12, would also be measured.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Neoplasms
Keywords
Colorectal Neoplasms, Dendritic Cells

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Dendritic Cells Vaccine
Arm Type
Experimental
Arm Description
Dendritic Cells Vaccine after 2 lines of chemotherapy
Arm Title
Supportive treatment
Arm Type
Other
Arm Description
Supportive treatment after 2 lines of chemotherapy
Intervention Type
Drug
Intervention Name(s)
Dendritic Cell Vaccine
Intervention Description
Vaccination with autologous dendritic cells loaded with autologous tumor antigens
Intervention Type
Other
Intervention Name(s)
Supportive treatment
Intervention Description
Supportive treatment after progression of the illness after 2 lines of chemotherapy
Primary Outcome Measure Information:
Title
Progression Free Survival
Time Frame
4 months
Secondary Outcome Measure Information:
Title
Overall Survival
Time Frame
4 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age over 18 years. Capacity of understanding and signing the informed consent and to undergo the study procedures. Previously treated with 2 lines of chemotherapy. ECOG <= 2. Adequate renal, hepatic and bone marrow function Confirmed diagnosis of colorectal cancer with hepatic metastasis, suitable for biopsy. Availability of tumor tissue, for maturing dendritic cells RECIST.1 criteria Exclusion Criteria: Clinically relevant diseases or infections (HBV, HCV, HIV). Pregnant or breast feeding women. Immunosuppressant treatment. Concurrent cancer, with the exceptions allowed by the principal investigator (PI).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ramon Vilella, PhD
Organizational Affiliation
Fundació Clinic Recerca Biomédica
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital Clínic Barcelona
City
Barcelona
ZIP/Postal Code
08036
Country
Spain

12. IPD Sharing Statement

Learn more about this trial

Randomized Trial With Dendritic Cells in Patients With Metastatic Colorectal Cancer

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