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Brief Title: Immunotherapy Study for Surgically Resected Pancreatic Cancer
Official Title: A Phase III Study of Chemotherapy and Chemoradiotherapy With or Without Algenpantucel-L (HyperAcute®-Pancreas) Immunotherapy in Subjects With Surgically Resected Pancreatic Cancer
Study ID: NCT01072981
Brief Summary: The purpose of this study is to assess overall survival after treatment with a regimen of adjuvant therapy (Gemcitabine alone or with 5-FU chemoradiation) with or without HyperAcute®-Pancreas (algenpantucel-L) immunotherapy in subjects who have undergone surgical resection.
Detailed Description: Unfortunately, despite the best clinical efforts and breakthroughs in biotechnology, most patients diagnosed with pancreatic cancer continue to die from the rapid progression of their disease. The primary reason for this is that the disease is typically without symptoms until significant local and/or distant spread has occurred and is often beyond the chance for cure at the time of the diagnosis. The lack of any treatment to significantly increase long term survival rates is reflected by the poor outcomes associated with this disease, specifically time to disease progression and overall survival. These disappointing facts typically shape discussions of treatment options for patients with this disease. However, another important part of the body is now being looked at as a target for therapy against this disease -- the immune system. Scientists have clearly shown that pancreatic tumor cells produce a number of defective proteins, or express normal proteins in highly uncharacteristic ways, as part of this cancer. In some cancers, these abnormalities can cause an immune response to the cancer cells much in the way one responds to infected tissue. In progressive cancers however, the immune system fails to identify or respond to these abnormalities and the cancer cells are not attacked or destroyed for reasons not yet fully understood. This clinical trial proposes a new way to stimulate the immune system to recognize the abnormal components found in pancreatic cancer cells and to stimulate an immune response that destroys or blocks the growth of the cancer. This new method of treatment helps the immune system of pancreatic cancer patients to "identify" the cancerous tissue so that it can be eliminated from the body. As an example, most people are aware that patients with certain diseases may require an organ transplant to replace a damaged kidney or heart. After receiving their transplant these patients receive special drugs because they are at great danger of having an immune response that destroys or "rejects" the transplanted organ. This "rejection" occurs when their immune system responds to differences between the cells of the transplanted organ and their own immune system by attacking the foreign tissue in the same way as it would attack infected tissue. When the differences between foreign tissues and the patient's body are even larger, perhaps like differences between organs from pigs and the immune system cells of humans, the rejection is very rapid, highly destructive and the immunity it generates is long lasting. This is called hyperacute rejection and the medicine used to immunize patients in this protocol tries to harness this response to teach a patient's immune system to fight their pancreatic cancer just as the body would learn to reject a transplanted organ from an animal. To do this, the investigators have placed a mouse gene into human pancreatic cancer cells so that the immune system will easily recognize them as foreign, stimulating the patient immune system to attack the vaccine cells just as they would any other animal cells. As part of the process of destroying the immunotherapy cells, the patient immune system is stimulated to identify as many differences from normal human as possible. This extra stimulation is thought to encourage immune responses against the pancreatic cancer in the patient based on shared abnormalities of pancreatic cancer vaccine cells and the patient's pancreatic cancer cells. In this experimental therapy, patients are given injections of an immunotherapy consisting of two types of cancer cells that the investigators have modified to make them more easily recognized and attacked by the immune system. The investigators propose to test this new treatment in patients with pancreatic cancer who have undergone tumor removal surgery but remain at extremely high risk of disease progression to demonstrate that treatment with the immunotherapy increases the time until the tumor recurs or increases overall survival when given in combination with the current standard of care therapy for this disease. For more information, please see our study specific website: www.pancreaticcancer-clinicaltrials.com
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
University of Alabama, Birmingham, Alabama, United States
University of South Alabama, Mobile, Alabama, United States
Arizona Cancer Center, Tucson, Arizona, United States
University of Arkansas for Medical Sciences, Little Rock, Arkansas, United States
City of Hope National Medical Center, Duarte, California, United States
University of Southern California, Los Angeles, California, United States
Cedars-Sinai Medical Center, Los Angeles, California, United States
Stanford Cancer Center, Palo Alto, California, United States
Sutter Institute for Medical Research, Sacramento, California, United States
California Pacific Medical Center, San Francisco, California, United States
University of Colorado, Aurora, Colorado, United States
Stamford Hospital, Stamford, Connecticut, United States
Georgetown University, Washington, District of Columbia, United States
Boca Raton Hospital, Boca Raton, Florida, United States
University of Florida, Gainesville, Florida, United States
Mayo Clinic, Jacksonville, Florida, United States
Lakeland Regional Cancer Center, Lakeland, Florida, United States
University of Miami, Miami, Florida, United States
USF Tampa General, Tampa, Florida, United States
MOFFITT, Tampa, Florida, United States
Illinois Cancer Specialists, Arlington Heights, Illinois, United States
Northwestern University, Chicago, Illinois, United States
Northshore University Health Systems, Evanston, Illinois, United States
Edward H. Kaplan, MD and Associates, Skokie, Illinois, United States
Indiana University Health Goshen Center for Cancer Care, Goshen, Indiana, United States
Indiana University, Indianapolis, Indiana, United States
Investigative Clinical Research of Indiana, LLC, Indianapolis, Indiana, United States
University of Iowa, Iowa City, Iowa, United States
University of Kansas Cancer Center, Westwood, Kansas, United States
University of Louisville, Louisville, Kentucky, United States
Mary Bird Perkins Cancer Center, Baton Rouge, Louisiana, United States
Ochsner Cancer Institute, New Orleans, Louisiana, United States
University of Maryland, Baltimore, Maryland, United States
Massachusetts General Hospital, Boston, Massachusetts, United States
Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States
Dana-Farber Cancer Institute, Boston, Massachusetts, United States
Lahey Clinic, Burlington, Massachusetts, United States
University of Michigan, Ann Arbor, Michigan, United States
Henry Ford Hospital, Detroit, Michigan, United States
Beaumont Hospital, Royal Oak, Michigan, United States
Virginia Piper Cancer Institute, Minneapolis, Minnesota, United States
Mayo Clinic, Rochester, Minnesota, United States
University of Missouri, Columbia, Missouri, United States
Washington University, Saint Louis, Missouri, United States
University of Nebraska Medical Center, Omaha, Nebraska, United States
University of New Mexico, Albuquerque, New Mexico, United States
Mount Sinai Medical Center, New York, New York, United States
Columbia University, New York, New York, United States
Duke University Medical Center, Durham, North Carolina, United States
Wake Forest Baptist Health Comprehensive Cancer Center, Winston-Salem, North Carolina, United States
University of Cincinnati, Cincinnati, Ohio, United States
University Hospitals Case Western, Cleveland, Ohio, United States
Ohio State University, Columbus, Ohio, United States
University of Oklahoma, Oklahoma City, Oklahoma, United States
Oregon Health and Science University, Portland, Oregon, United States
St. Luke's Hospital and Health Network, Bethlehem, Pennsylvania, United States
Penn State Hershey Cancer Institute, Hershey, Pennsylvania, United States
University of Pennsylvania, Philadelphia, Pennsylvania, United States
Thomas Jefferson University, Philadelphia, Pennsylvania, United States
Fox Chase Cancer Center, Philadelphia, Pennsylvania, United States
University of Pittsburg Medical Center, Pittsburgh, Pennsylvania, United States
Roger Williams Medical Center, Providence, Rhode Island, United States
Greenville Health System, Greenville, South Carolina, United States
University of Texas Southwestern Medical Center, Dallas, Texas, United States
Baylor College of Medicine, Houston, Texas, United States
Ben Taub Hospital, Houston, Texas, United States
The Methodist Hospital, Houston, Texas, United States
Joe Arrington Cancer Research and Treatment Center, Lubbock, Texas, United States
University of Texas Health Sciences, San Antonio, Texas, United States
University of Virginia, Charlottesville, Virginia, United States
Lynchburg Hematology-Oncology Clinic, Inc., Lynchburg, Virginia, United States
Virginia Commonwealth University, Richmond, Virginia, United States
University of Washington- Seattle Cancer Center Alliance, Seattle, Washington, United States
Vince Lombardi Cancer Clinic, Green Bay, Wisconsin, United States
University of Wisconsin, Madison, Wisconsin, United States