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Carcinoembryonic Antigen-loaded Dendritic Cells in Advanced Colorectal Cancer Patients

Primary Purpose

Colorectal Cancer, Liver Metastases

Status
Completed
Phase
Phase 1
Locations
Netherlands
Study Type
Interventional
Intervention
CEA-loaded dendritic cell vaccine
Sponsored by
Radboud University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Colorectal Cancer focused on measuring Dendritic cells, Colorectal cancer, Carcinoembryonic antigen, Vaccine, Immunotherapy

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

For arm A and B Inclusion Criteria: Histological documented evidence of colorectal cancer. Primary tumor surgically removed, recurrence(s) in the liver. Planned surgical excision of liver metastases. HLA-A2.1 phenotype according to lymphocyte HLA typing. Expression of CEA on primary tumor. ECOG performance status 0-1, life expectancy > 3 months. Age 18-75 years. WBC > 3.0 x 109/l, lymphocytes > 0.8 x 109/l, platelets > 100 x 109/l, serum creatinine < 150 μmol/l, serum bilirubin < 25 μmol/l. Expected adequacy of follow-up. Written informed consent. Exclusion Criteria: Clinical signs of extra hepatic metastases, in patients with a clinical suspicion of other metastases diagnostic tests should be performed to exclude this. Prior chemotherapy, immunotherapy, or radiotherapy within three months before planned surgical excision is allowed. A history of myocardial infarction, angina pectoris, cardiac arrhythmias, cerebrovascular accidents, transient ischemic attacks or severe hypertension (exclusion criteria for autologous blood donation) Concomitant use of corticosteroids or other immunosuppressive agents. A history of any second malignancy in the past five years excluding adequately treated basal carcinoma of skin or carcinoma in situ of cervix. Serious concomitant disease, active infections. Specifically, patients with autoimmune disease or organ allografts and patients with a history of HBsAg or HIV are excluded. A known allergy to shell fish. Pregnant or lactating women. For arm C (side-study) inclusion criteria: histological proof of colorectal cancer HLA-A0201 positive stage III (T1-4N1-2M0) cancer or high risk stage II (T4 and/or poor differentiation in histology and/or perforation and/or obstruction and/or venous invasion and/or histological analysis of ≤10 lymph nodes) ≤ 8 weeks since surgical resection of primary colorectal tumor Age 18-75 years WHO performance 0-1 (Karnofsky 100-70%) WBC ≥ 3.0x109/l Platelets ≥ 100x109/l Hb ≥ 6 mmol/l Total bilirubin ≤ 2x UNL ASAT and ALAT ≤ 3x UNL Serum creatinine ≤ 1.5 x UNL Expected adequacy of follow-up Signed written informed consent exclusion criteria A history of second malignancy within the last 5 years. Adequately treated basal carcino¬ma of skin or carcinoma in situ of cervix is acceptable within this period Serious concomitant disease. Autoimmune disease or organ grafts. Other serious concomitant diseases preventing the safe administration of study drugs or likely to interfere with the study assessments. A known allergy to shell fish (contains KLH) Pregnant or lactating women

Sites / Locations

  • Radboud University Nijmegen Medical Center, dept. of Medical Oncology

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Active Comparator

Experimental

Experimental

Arm Label

A

B

C

Arm Description

Dendritic cells pulsed with CEA-peptide

Dendritic cells electroporated with CEA-mRNA

Dendritic cells pulsed with CEA-peptide, in combination with oxaliplatin/capecitabine

Outcomes

Primary Outcome Measures

immunological response against carcinoembryonic antigen and the control protein KLH
Toxicity

Secondary Outcome Measures

Full Information

First Posted
September 27, 2005
Last Updated
November 26, 2010
Sponsor
Radboud University Medical Center
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1. Study Identification

Unique Protocol Identification Number
NCT00228189
Brief Title
Carcinoembryonic Antigen-loaded Dendritic Cells in Advanced Colorectal Cancer Patients
Official Title
Induction of Specific T Cell Responses in Colorectal Cancer Patients With Liver Metastases Upon Vaccination With Autologous Dendritic Cells Pulsed With CEA-peptide or Electroporated With CEA-RNA: Evaluation of in Vivo Immune Response.
Study Type
Interventional

2. Study Status

Record Verification Date
November 2010
Overall Recruitment Status
Completed
Study Start Date
December 2003 (undefined)
Primary Completion Date
November 2010 (Actual)
Study Completion Date
November 2010 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Radboud University Medical Center

4. Oversight

5. Study Description

Brief Summary
Dendritic cells (DCs) are the professional antigen-presenting cells of the immune system. As such they are currently used in clinical vaccination protocols in cancer patients. We evaluate the ability of mature DCs pulsed with carcinoembryonic antigen (CEA)-peptide (arm A) or electroporated with CEA-mRNA (arm B) to induce CEA-specific T cell responses in patients with resectable liver metastases from colorectal cancer. To evaluate immune responses, CEA-specific T cell reactivity is monitored in peripheral blood, resected abdominal lymph nodes, tumor tissue and biopsies of vaccination sites and post-treatment DTH skin tests. Patients are vaccinated intradermally and intravenously with CEA-peptide pulsed mature DCs three times prior to resection of liver metastases. In 2007 a side-study has been added (arm C), in which patients with stage III or high-risk stage II colorectal cancer that are amenable for standard adjuvant oxaliplatin/capecitabine therapy are vaccinated with CEApeptide-pulsed DCs. Also in this group, safety and immune responses in peripheral blood and the DTH-skin test are the primary endpoints. Results are compared with the results obtained in arm A.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer, Liver Metastases
Keywords
Dendritic cells, Colorectal cancer, Carcinoembryonic antigen, Vaccine, Immunotherapy

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
A
Arm Type
Active Comparator
Arm Description
Dendritic cells pulsed with CEA-peptide
Arm Title
B
Arm Type
Experimental
Arm Description
Dendritic cells electroporated with CEA-mRNA
Arm Title
C
Arm Type
Experimental
Arm Description
Dendritic cells pulsed with CEA-peptide, in combination with oxaliplatin/capecitabine
Intervention Type
Biological
Intervention Name(s)
CEA-loaded dendritic cell vaccine
Intervention Description
Carcinoembryonic antigen (either peptide or mRNA) loaded dendritic cells.
Primary Outcome Measure Information:
Title
immunological response against carcinoembryonic antigen and the control protein KLH
Time Frame
During the study
Title
Toxicity
Time Frame
During the study

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
For arm A and B Inclusion Criteria: Histological documented evidence of colorectal cancer. Primary tumor surgically removed, recurrence(s) in the liver. Planned surgical excision of liver metastases. HLA-A2.1 phenotype according to lymphocyte HLA typing. Expression of CEA on primary tumor. ECOG performance status 0-1, life expectancy > 3 months. Age 18-75 years. WBC > 3.0 x 109/l, lymphocytes > 0.8 x 109/l, platelets > 100 x 109/l, serum creatinine < 150 μmol/l, serum bilirubin < 25 μmol/l. Expected adequacy of follow-up. Written informed consent. Exclusion Criteria: Clinical signs of extra hepatic metastases, in patients with a clinical suspicion of other metastases diagnostic tests should be performed to exclude this. Prior chemotherapy, immunotherapy, or radiotherapy within three months before planned surgical excision is allowed. A history of myocardial infarction, angina pectoris, cardiac arrhythmias, cerebrovascular accidents, transient ischemic attacks or severe hypertension (exclusion criteria for autologous blood donation) Concomitant use of corticosteroids or other immunosuppressive agents. A history of any second malignancy in the past five years excluding adequately treated basal carcinoma of skin or carcinoma in situ of cervix. Serious concomitant disease, active infections. Specifically, patients with autoimmune disease or organ allografts and patients with a history of HBsAg or HIV are excluded. A known allergy to shell fish. Pregnant or lactating women. For arm C (side-study) inclusion criteria: histological proof of colorectal cancer HLA-A0201 positive stage III (T1-4N1-2M0) cancer or high risk stage II (T4 and/or poor differentiation in histology and/or perforation and/or obstruction and/or venous invasion and/or histological analysis of ≤10 lymph nodes) ≤ 8 weeks since surgical resection of primary colorectal tumor Age 18-75 years WHO performance 0-1 (Karnofsky 100-70%) WBC ≥ 3.0x109/l Platelets ≥ 100x109/l Hb ≥ 6 mmol/l Total bilirubin ≤ 2x UNL ASAT and ALAT ≤ 3x UNL Serum creatinine ≤ 1.5 x UNL Expected adequacy of follow-up Signed written informed consent exclusion criteria A history of second malignancy within the last 5 years. Adequately treated basal carcino¬ma of skin or carcinoma in situ of cervix is acceptable within this period Serious concomitant disease. Autoimmune disease or organ grafts. Other serious concomitant diseases preventing the safe administration of study drugs or likely to interfere with the study assessments. A known allergy to shell fish (contains KLH) Pregnant or lactating women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Prof. dr. C.J.A. Punt, MD,PhD
Organizational Affiliation
Radboud University Nijmegen Medical Center, dept. of Medical Oncology
Official's Role
Principal Investigator
Facility Information:
Facility Name
Radboud University Nijmegen Medical Center, dept. of Medical Oncology
City
Nijmegen
ZIP/Postal Code
P.O. box 9101 6500 HB
Country
Netherlands

12. IPD Sharing Statement

Citations:
PubMed Identifier
15122249
Citation
Figdor CG, de Vries IJ, Lesterhuis WJ, Melief CJ. Dendritic cell immunotherapy: mapping the way. Nat Med. 2004 May;10(5):475-80. doi: 10.1038/nm1039.
Results Reference
background
PubMed Identifier
18262431
Citation
Lesterhuis WJ, Aarntzen EH, De Vries IJ, Schuurhuis DH, Figdor CG, Adema GJ, Punt CJ. Dendritic cell vaccines in melanoma: from promise to proof? Crit Rev Oncol Hematol. 2008 May;66(2):118-34. doi: 10.1016/j.critrevonc.2007.12.007. Epub 2008 Feb 8.
Results Reference
background
PubMed Identifier
16110035
Citation
de Vries IJ, Bernsen MR, Lesterhuis WJ, Scharenborg NM, Strijk SP, Gerritsen MJ, Ruiter DJ, Figdor CG, Punt CJ, Adema GJ. Immunomonitoring tumor-specific T cells in delayed-type hypersensitivity skin biopsies after dendritic cell vaccination correlates with clinical outcome. J Clin Oncol. 2005 Aug 20;23(24):5779-87. doi: 10.1200/JCO.2005.06.478.
Results Reference
background
PubMed Identifier
16600979
Citation
Lesterhuis WJ, de Vries IJ, Schuurhuis DH, Boullart AC, Jacobs JF, de Boer AJ, Scharenborg NM, Brouwer HM, van de Rakt MW, Figdor CG, Ruers TJ, Adema GJ, Punt CJ. Vaccination of colorectal cancer patients with CEA-loaded dendritic cells: antigen-specific T cell responses in DTH skin tests. Ann Oncol. 2006 Jun;17(6):974-80. doi: 10.1093/annonc/mdl072. Epub 2006 Apr 6.
Results Reference
result
PubMed Identifier
21187495
Citation
Lesterhuis WJ, De Vries IJ, Schreibelt G, Schuurhuis DH, Aarntzen EH, De Boer A, Scharenborg NM, Van De Rakt M, Hesselink EJ, Figdor CG, Adema GJ, Punt CJ. Immunogenicity of dendritic cells pulsed with CEA peptide or transfected with CEA mRNA for vaccination of colorectal cancer patients. Anticancer Res. 2010 Dec;30(12):5091-7.
Results Reference
derived
Links:
URL
http://www.umcn.nl
Description
Home page of the Radboud University Nijmegen Medical Center

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Carcinoembryonic Antigen-loaded Dendritic Cells in Advanced Colorectal Cancer Patients

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