Abstract
Chronic graft-versus-host-disease (cGVHD) is the major cause of late morbidity and mortality after allogeneic stem cell transplantation. B cells have been reported to be involved in mediating cGVHD. To assess whether preemptive host B cell depletion prevents extensive cGVHD after allogeneic reduced-intensity conditioning transplantation (RICT), 173 patients treated with RICT for various hematologic diseases, who had or had not received Rituximab (Rtx) within 6 month prior to RICT, were analyzed retrospectively. Rtx treatment within 6 months prior to RICT reduced extensive cGVHD significantly from 45.8% to 20.1%. We hypothesize that most likely host B cells initiate cGVHD, and thus, host B cell depletion prior to RICT by Rtx might be a valuable strategy to reduce extensive cGVHD after RICT.
Publication types
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Comparative Study
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Evaluation Study
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Research Support, Non-U.S. Gov't
MeSH terms
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Adult
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Aged
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Alemtuzumab
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Antibodies, Monoclonal / administration & dosage
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Antibodies, Monoclonal / therapeutic use*
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Antibodies, Monoclonal, Humanized
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Antibodies, Monoclonal, Murine-Derived
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Antibodies, Neoplasm / therapeutic use
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Antilymphocyte Serum / administration & dosage
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Antineoplastic Combined Chemotherapy Protocols / therapeutic use
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B-Lymphocytes / drug effects*
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B-Lymphocytes / immunology
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Chronic Disease
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Combined Modality Therapy
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Disease-Free Survival
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Drug Administration Schedule
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Female
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Graft vs Host Disease / drug therapy
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Graft vs Host Disease / etiology
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Graft vs Host Disease / prevention & control*
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Hematologic Diseases / drug therapy
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Hematologic Diseases / surgery*
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Humans
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Immunosuppressive Agents / therapeutic use
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Incidence
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Kaplan-Meier Estimate
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Lymphocyte Depletion / methods*
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Male
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Middle Aged
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Patient Selection
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Premedication
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Retrospective Studies
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Rituximab
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Sample Size
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Transplantation Conditioning / methods*
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Young Adult
Substances
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Antibodies, Monoclonal
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Antibodies, Monoclonal, Humanized
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Antibodies, Monoclonal, Murine-Derived
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Antibodies, Neoplasm
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Antilymphocyte Serum
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Immunosuppressive Agents
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Alemtuzumab
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Rituximab