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Advances in the Management of Transplant-Related Toxicity |
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A Focus on Graft-Versus-Host Disease
and the Use of Reduced-Intensity
Conditioning Regimens
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Hematopoietic stem cell transplantation (HSCT) is a commonly used and
effective treatment option for a wide range of hematologic malignancies,
with approximately 8,000 allogeneic bone marrow transplants performed
annually in the United States. The successful engraftment of an allogeneic
HSCT requires immunosuppression of the recipient through the use of a
preparative regimen. Traditionally, a myeloablative regimen, including
chemotherapy with or without total body irradiation (TBI) has been used.
While myeloablative therapy can successfully produce engraftment, these
regimens impart significant toxicity, limiting their use in patients who are
older or have comorbidities. Recently, nonmyeloablative regimens have
been investigated that provide sufficient immunosuppression of the recipient,
allowing for engraftment and development of the graft-versusmalignancy
effect. Nonmyeloablative regimens can include purine
analogs combined with an alkylating agent or low-dose TBI. While these
regimens appear effective, potential complications include the development
of graft-versus-host disease (GVHD) and low donor chimerism. This
monograph will focus on updates on the use of nonmyeloablative transplantation
in the treatment of hematologic malignancies and the management
of potential associated adverse events.
Download a PDF version of the monograph
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Contributing Editor:
Mary Evelyn D. Flowers, MD
Director, Clinical LTFU
Associate Professor, UW
Fred Hutchinson Cancer Research Center
University of Washington
Release date: May 18, 2006
Expiration date: May 18, 2007
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