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2004 JAN 7 - (NewsRx.com & NewsRx.net) -- Genitope Corp. (GTOP) announced results of a phase II clinical trial evaluating MyVax Personalized Immunotherapy for the treatment of aggressive non-Hodgkin lymphoma, including mantle cell lymphoma (MCL).
The data were presented at the American Society of Hematology's 45th annual meeting and exposition by John P. Leonard, MD, assistant professor of medicine at Weill Cornell Medical College of Cornell University, and medical director of oncology services at New York-Presbyterian Hospital/Weill Cornell Medical Center.
The study examined two dosing strategies of MyVax Personalized Immunotherapy. The data suggest an accelerated schedule with more doses of MyVax Personalized Immunotherapy may be a safe and effective treatment following chemotherapy in individuals with aggressive lymphoma, including mantle cell lymphoma.
"Patients with mantle cell lymphoma typically respond well to chemotherapy, but the disease has the shortest median survival of all lymphoma subtypes and generally recurs quickly," said Leonard. "This study is an important step in the right direction, as we need to find an effective treatment for this difficult disease."
The study involved 27 patients with aggressive non-Hodgkin lymphoma, in complete or partial remission following CHOP chemotherapy. Each patient received one of two treatment schedules of MyVax Personalized Immunotherapy. Fourteen patients on Schedule A (5 with MCL) received five immunizations over 24 weeks, starting 3 months after completing chemotherapy.
The median time to ...