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Randomized Trial With Dendritic Cells in Patients With Metastatic Colorectal Cancer

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

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01413295
Enrollment
52
Registered
2011-08-10
Start date
2011-08-31
Completion date
2014-09-30
Last updated
2014-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Colorectal Neoplasms

Keywords

Colorectal Neoplasms, Dendritic Cells

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.

Interventions

Vaccination with autologous dendritic cells loaded with autologous tumor antigens

Supportive treatment after progression of the illness after 2 lines of chemotherapy

Sponsors

Fundacion Clinic per a la Recerca Biomédica
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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).

Design outcomes

Primary

MeasureTime frame
Progression Free Survival4 months

Secondary

MeasureTime frame
Overall Survival4 months

Countries

Spain

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026