The purpose of this study is to identify approximately 100 - 150 patients who have received Vectibix (Panitumumab) in offices and clinics located in Tennessee, North Carolina, South Carolina, and North Georgia from February 2004 - April 2009. Information regarding the incidence and severity of hypersensitivity infusion reactions to Vectibix (Panitumumab)will be captured. In patients who experienced hypersensitivity reactions, the following information will also be collected: premedication, treatment cycle symptoms that were experienced during chemotherapy, changes required in subsequent Vectibix (Panitumumab) or chemotherapy treatment, and outcome of the hypersensitivity reaction.
Study Type
OBSERVATIONAL
Enrollment
141
Northeast Arkansas Clinic
Jonesboro, Arkansas, United States
Medical Oncology Associates of Augusta
Augusta, Georgia, United States
Northeast Georgia Medical Center
Gainesville, Georgia, United States
Baptist Hospital East
Louisville, Kentucky, United States
St. Louis Cancer Care
Chesterfield, Missouri, United States
South Carolina Oncology Associates, PA
Columbia, South Carolina, United States
Tennessee Oncology, PLLC
Nashville, Tennessee, United States
Rate of Vectibix-related infusion reactions w/high rate of Erbitux-related infusion reactions
To determine the rate of Vectibix (Panitumumab)-related infusion reactions (CTCAE v3.0 grade I-IV) in geographic areas of the United States associated with a high rate of Erbitux-related infusion reactions
Time frame: February 2004 -April 2009
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