Immunotherapy for Colorectal Cancers Using CEA-Pulsed Dendritic Cells and Subsequent IL-2 Treatment

Phase 1

• Conditions: Colorectal Cancer

• Registration Number: NCT00154713
• Lead Sponsor: National Taiwan University Hospital

Brief Summary

The specific aims of this study are as follows:

1. Primary endpoint: to evaluate the clinical responses of vaccinated patients.

2. Secondary endpoint: to evaluate the safety of this treatment and the immune responses against CEA before and after the treatment

Detailed Description

In this trial, we will immunize metastatic colorectal cancer patients with recombinant CEA-pulsed DCs mixed with tetanus toxoid by subcutaneous injection. Low dose IL-2 will be given subcutaneously following DC vaccination to boost the growth of T cells. We will adapt "Simon's optimal two-stage design" for this study. In the first stage, we will treat 12 patients to evaluate the safety of this new protocol. If there are no severe toxicities/side effects and there is at least one patient that had stable disease or better clinical response, then we will proceed to the second stage and treat additional 25 patients. We will follow the clinical outcome of these 37 patients. The immune responses against CEA before and after vaccination will be examined.

Study Timeline

• Status Verified: 2005-07
• Study Start: 2005-07
• Study Completion: 2005-07
• Study First Submitted: 2005-09-08
• Study First Submitted QC: 2005-09-08
• Last Update Submitted: 2005-09-08
• Study First Posted: 2005-09-12
• Last Update Posted: 2005-09-12

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 37

Inclusion Criteria

• Patients must have metastatic colorectal cancer.
• Patients must have at least one measurable lesion.
• Patients'serum level of CEA must be higher than 5 times of the normal value
• Patients'disease must have failed chemotherapy with 5FU, CPT-11 or oxaliplatin.
• Patients who are unsuitable or refuse chemotherapy will be considered eligible for this trial.
• Patients'age must be 20 or greater.
• Patients'estimated life expectancy is more than 3 months.
• Patients must have adequate bone marrow function, defined as WBC >= 3500/mm3, neutrophil >= 1500/mm3, lymphocyte >= 1,000/mm3, and platelet >= 100,000/mm3.
• Patients must have adequate liver and renal function, defined as serum alanine transaminase (ALT) and aspartate transaminase (AST) =< 5 times normal, bilirubin =< 1.5 times normal range, and creatinine =< 2 times upper normal limit.
• All patients should have documentation of negative result of penicillin test.
• Women or men of reproductive potential may not participate unless they have agreed to use an effective contraceptive method.
• All patients must be informed of the investigational nature of this study and must sign and give written informed consent.

Exclusion Criteria

• Patients who have central nervous system metastasis except for those whose CNS disease has been treated with radiotherapy and/or surgery and has been stable for at least two weeks
• Patients who have active acute or chronic infection (at the discretion of the investigator).
• Pregnant or breast-nursing women
• Patients who have active cardiac disease requiring therapy for failure, angina, arrythmia, or infarction within the preceding 6 months (exception: any patient whose cardiac failure is compensated on medications)
• Patients who have asthma
• Patients who have autoimmune disease such as inflammatory bowel disease, lupus erythematosus, ankylosing spondylitis, scleroderma, and multiple sclerosis
• Patients who have serious concomitant systemic disorders incompatible with the study (at the discretion of the investigator)
• Patients who have other prior or concurrent malignancy except for in-situ-carcinoma of cervix or adequately treated basal cell carcinoma of skin.
• Patients who received chemotherapy, steroid or biologic treatment within 4 weeks prior to enrollment

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Primary Outcome Measures

Name	Time	Method
evaluate the clinical responses of vaccinated patients 6 weeks after the first injection

Secondary Outcome Measures

Name	Time	Method
evaluate the safety of this treatment and the immune responses against CEA before and after the treatment 6 weeks after the first injection

Trial Locations

Locations (1)

National Taiwan University Hospital; 🇨🇳 Taipei, Taiwan