A Pilot Study Assessing Intra-Metastasis Administration of Autologous KLH-pulsed Dendritic Cells With Tumoral Radiation Therapy in Patients With Metastatic Pancreatic Carcinoma

University of Michigan Rogel Cancer Center

Status and phase

Terminated

Phase 1

Conditions

Metastatic Pancreatic Carcinoma

Treatments

Radiation: tumoral irradiation

Biological: Dendritic cell vaccination

Study type

Interventional

Funder types

Other

Identifiers

NCT00843830

UMCC 2005.135

Details and patient eligibility

About

This study is being done to determine whether it is possible to use an investigational vaccine that consists of dendritic cells in patients with pancreas cancer. Dendritic cells are immune cells that are obtained from your blood that are important in the body's immune response to foreign substances. The vaccine would be injected directly into a tumor that has spread to the liver after a short course of radiation therapy has been given to that tumor. The study will try to determine if this treatment would be safe and effective in treating this cancer.

This is a phase 1 pilot study of this treatment. Phase 1 trials test the best way to give a treatment where little is known about its possible risks or benefits. Phase 2 studies then test the possible benefits of a treatment and may show the specific situations where they are seen. Promising treatments are then tested in Phase 3 trials which compare the new treatment to standard treatment in a larger group of patients. Phase 4 trials are those conducted on a treatment after it has been approved for general use outside of research. A pilot study tests a treatment in a small number of patients to learn if and how the treatment could be tested in a larger group. Pilot studies can be performed at any phase but are commonly performed in the earliest phases of research on a treatment.

Enrollment

4 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Pathologic diagnosis of pancreatic carcinoma
Radiologic evidence of hepatic metastasis with at least one lesion > 2.0 cm that is amenable to ultrasound or CT guided intra-tumoral DC injection
Age > 18
Life expectancy > 3 months
Karnofsky Performance Status > 70%
Patients must not have received any anti-neoplastic chemotherapy, immunotherapy or radiotherapy for the four weeks preceding entry onto the study (six weeks for nitrosoureas and mitomycin C).
Adequate baseline hematopoietic function defined as WBC (white blood cell) > 3000/mm3, hemoglobin > 9g/dl, and platelet count > 100,000/mm3.
Adequate baseline organ function defined as creatinine < 2.0, total bilirubin < 2.0 mg/dl
Patients taking warfarin are not eligible. Adequate coagulation function defined as PT (prothrombin time) < 15, INR < 1.5 and PTT (partial thromboplastin time) < 35.
Ability to give informed consent

Exclusion criteria

Previous anti-tumor vaccine therapy
Prior hepatic irradiation
Known brain metastases
History of prior autoimmune diseases (e.g. SLE (systemic lupus erythematosus), rheumatoid arthritis, myasthenia gravis)
Regular corticosteroid use within the past one year or any corticosteroid use in the four weeks preceding study entry
Evidence of HIV infection, AIDS, Hepatitis B or Hepatitis C infection
Active bacterial, fungal or viral infection
Pregnancy or lactation; women of childbearing potential and men must agree to use effective contraception during the course of this clinical trial
Uncontrolled or unstable medical conditions including angina, arrhythmias, bleeding, or thromboembolic conditions,
Any medical or psychiatric illness that might compromise the patients ability to tolerate treatment