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Allogeneic Transplantation for Hodgkin’s Lymphoma

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Allogeneic Stem Cell Transplantation

Part of the book series: Contemporary Hematology ((CH))

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Abstract

There are only approximately 7,500 cases of Hodgkin’s lymphoma diagnosed in the United States annually. While there is a bimodal distribution in incidence, the majority of cases occur in young adults 15-30 years of age [1]. Initial therapy is highly successful with progression-free survival (PFS) rates at 10 years of 70-90% for early stage disease and 60-70% for advanced disease. For those relapsing after initial therapy, 30-50% are long-term survivors after an autologous stem cell transplant, making this one of the most curable adult malignancies. However, a small minority of these typically young and otherwise healthy patients will relapse even after an autologous stem cell transplantation (ASCT) and it is for these rare patients that allogeneic transplantation has been increasingly considered. Initially discarded in the early 1990s as being too toxic utilizing myeloablative conditioning, allogeneic transplantation for this disease is increasing again based on the availability of reduced intensity regimens and therapies that have decreased mortality due to regimen-related toxicities, graft versus host disease (GVHD), and opportunistic infections. Whether or not this will be an effective approach for multiply resistant patients remains to be determined, making this one of the most controversial areas in 2008 in allogeneic transplantation. This chapter outlines modern therapy for this group of lymphomas and the potential utility of allogeneic transplantation in select patients.

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Broderick, W., Stiff, P. (2010). Allogeneic Transplantation for Hodgkin’s Lymphoma. In: Lazarus, H.M., Laughlin, M.J. (eds) Allogeneic Stem Cell Transplantation. Contemporary Hematology. Humana Press. https://doi.org/10.1007/978-1-59745-478-0_6

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  • DOI: https://doi.org/10.1007/978-1-59745-478-0_6

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  • Print ISBN: 978-1-934115-33-6

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