Vaccine Therapy in Treating Patients With Colorectal, Stomach, or Pancreatic Cancer

Completed · Phase 1

Conditions studied: Recurrent Colon Cancer, Recurrent Gastric Cancer, Recurrent Pancreatic Cancer, Recurrent Rectal Cancer, Stage III Colon Cancer, Stage III Gastric Cancer, Stage III Pancreatic Cancer, Stage III Rectal Cancer, Stage IV Colon Cancer, Stage IV Gastric Cancer, Stage IV Pancreatic Cancer, Stage IV Rectal Cancer

In brief

RATIONALE: Vaccines made from a gene-modified virus may help the body build an effective immune response to kill tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of vaccine therapy in treating patients with colorectal, stomach, or pancreatic cancer.

Key facts

Study ID

NCT01191684

Run by

City of Hope Medical Center

People needed

12

Starts

2011-10-01

Expected to finish

2013-08-01

Last updated by the study team

2017-08-01

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients with unresectable and chemotherapy resistant primary or recurrent carcinoma of colorectal, gastric or pancreatic origin
• There must be pathologic evidence for malignancy with a soft tissue component of tumor evident on CT scan imaging or physical examination
• Patient must be able to give informed consent
• There must be an anticipated survival of at least 3 months
• Performance status of 80-100 (Karnofsky performance status)
• WBC count >= 3,000uL
• Platelet count >= 100,000uL
• Prothrombin time and partial thromboplastin time of <= 1.5 times the upper limit of normal
• Women of childbearing potential must have a negative pregnancy test; women and men of childbearing potential must agree to use adequate contraception (hormonal or barrier method of birth control or abstinence) prior to study entry and for six months following duration of study participation; should a woman become pregnant during or suspect that she is pregnant while participating on the trial, she should inform her treating physician immediately
• Patients with asymptomatic small volume bone disease not likely to require radiation therapy during the period of the vaccine trial will be eligible
• Hemoglobin level > 9g/dL
• There must be evidence of p53 over expression by immunohistochemistry with > 10% of cells within the tumor strongly positive
• Patients with colorectal cancer will need to have failed to respond to 5-FU based therapy with oxaliplatin, irinotecan as well as epidermal growth factor receptor (EGFR) directed therapies (if appropriate); patients with gastric cancer will need to have progressed on standard first line chemotherapy or chemoradiotherapy and Herceptin based therapy (if appropriate); patients with pancreatic cancer who have failed to respond to at least 1 chemotherapy regimen

You may not qualify if…

• Diagnosis which has been associated with immunodeficiency, including HIV
• Prior radiation to more than 50% of all nodal groups
• Concurrent use of corticosteroids
• History of another malignancy, other than nonmelanoma skin cancer in the past 2 years
• Recent major surgery
• Serious intercurrent illness
• Temperature >= 101F within 3 days prior to the initial injection
• Pregnancy or lactation
• Clinically evident brain metastasis
• Autoimmune disease
• HIV seropositivity or refusal to hear the results of the HIV test
• Receipt of organ grafts
• History of severe environmental allergies
• History of severe neurological, cardiovascular, renal, hepatic, endocrine, respiratory, or bone marrow dysfunction requiring frequent re-evaluation, and management by a physician
• Patients with a history of congestive heart failure or coronary artery disease which has not been resolved by bypass or stent
• History of myopericarditis
• Known family history of Li-Fraumeni syndrome
• Allergy to egg proteins
• Chemotherapy or radiation within the 4 weeks preceding enrollment

Where it is running

• City of Hope Medical Center — Duarte, California, United States

Full record on ClinicalTrials.gov

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