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Outcomes of a 1-day nonmyeloablative salvage regimen for patients with primary graft failure after allogeneic hematopoietic cell transplantation

Primary graft failure after allogeneic hematopoietic cell transplantation is a life-threatening complication. A shortened conditioning regimen may reduce the risk of infection and increase the chance of survival. Here, we report the outcome of 11 patients with hematologic diseases (median age, 44; r...

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Autores principales: Kanda, Junya, Horwitz, Mitchell E., Long, Gwynn D., Gasparetto, Cristina, Sullivan, Keith M., Chute, John P., Morris, Ashley, Hennig, Therese, Li, Zhiguo, Chao, Nelson J., Rizzieri, David A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214602/
https://www.ncbi.nlm.nih.gov/pubmed/21804612
http://dx.doi.org/10.1038/bmt.2011.158
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author Kanda, Junya
Horwitz, Mitchell E.
Long, Gwynn D.
Gasparetto, Cristina
Sullivan, Keith M.
Chute, John P.
Morris, Ashley
Hennig, Therese
Li, Zhiguo
Chao, Nelson J.
Rizzieri, David A.
author_facet Kanda, Junya
Horwitz, Mitchell E.
Long, Gwynn D.
Gasparetto, Cristina
Sullivan, Keith M.
Chute, John P.
Morris, Ashley
Hennig, Therese
Li, Zhiguo
Chao, Nelson J.
Rizzieri, David A.
author_sort Kanda, Junya
collection PubMed
description Primary graft failure after allogeneic hematopoietic cell transplantation is a life-threatening complication. A shortened conditioning regimen may reduce the risk of infection and increase the chance of survival. Here, we report the outcome of 11 patients with hematologic diseases (median age, 44; range, 25–67 years, 7 males) who received a 1-day reduced-intensity preparative regimen given as a re-transplantation for primary graft failure. The salvage regimen consisted of fludarabine, cyclophosphamide, alemtuzumab, and total-body irradiation, all administered 1 day before re-transplantation. All patients received T-cell replete peripheral blood stem cells from the same or different haploidentical donor (n = 10) or from the same matched sibling donor (n = 1). Neutrophil counts promptly increased to >500/µL for 10 of the 11 patients at a median of 13 days. Of these, none developed Grade III/IV acute graft-versus-host disease. At present, 8 of the 11 patients are alive with a median follow-up of 11.2 months from re-transplantation and 5 of the 8 are in remission. In conclusion, this series suggests that our 1-day preparative regimen is feasible, leads to successful engraftment in a high proportion of patients, and is appropriate for patients requiring immediate re-transplantation after primary graft failure following reduced-intensity transplantation.
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spelling pubmed-32146022012-11-01 Outcomes of a 1-day nonmyeloablative salvage regimen for patients with primary graft failure after allogeneic hematopoietic cell transplantation Kanda, Junya Horwitz, Mitchell E. Long, Gwynn D. Gasparetto, Cristina Sullivan, Keith M. Chute, John P. Morris, Ashley Hennig, Therese Li, Zhiguo Chao, Nelson J. Rizzieri, David A. Bone Marrow Transplant Article Primary graft failure after allogeneic hematopoietic cell transplantation is a life-threatening complication. A shortened conditioning regimen may reduce the risk of infection and increase the chance of survival. Here, we report the outcome of 11 patients with hematologic diseases (median age, 44; range, 25–67 years, 7 males) who received a 1-day reduced-intensity preparative regimen given as a re-transplantation for primary graft failure. The salvage regimen consisted of fludarabine, cyclophosphamide, alemtuzumab, and total-body irradiation, all administered 1 day before re-transplantation. All patients received T-cell replete peripheral blood stem cells from the same or different haploidentical donor (n = 10) or from the same matched sibling donor (n = 1). Neutrophil counts promptly increased to >500/µL for 10 of the 11 patients at a median of 13 days. Of these, none developed Grade III/IV acute graft-versus-host disease. At present, 8 of the 11 patients are alive with a median follow-up of 11.2 months from re-transplantation and 5 of the 8 are in remission. In conclusion, this series suggests that our 1-day preparative regimen is feasible, leads to successful engraftment in a high proportion of patients, and is appropriate for patients requiring immediate re-transplantation after primary graft failure following reduced-intensity transplantation. 2011-08-01 2012-05 /pmc/articles/PMC3214602/ /pubmed/21804612 http://dx.doi.org/10.1038/bmt.2011.158 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Kanda, Junya
Horwitz, Mitchell E.
Long, Gwynn D.
Gasparetto, Cristina
Sullivan, Keith M.
Chute, John P.
Morris, Ashley
Hennig, Therese
Li, Zhiguo
Chao, Nelson J.
Rizzieri, David A.
Outcomes of a 1-day nonmyeloablative salvage regimen for patients with primary graft failure after allogeneic hematopoietic cell transplantation
title Outcomes of a 1-day nonmyeloablative salvage regimen for patients with primary graft failure after allogeneic hematopoietic cell transplantation
title_full Outcomes of a 1-day nonmyeloablative salvage regimen for patients with primary graft failure after allogeneic hematopoietic cell transplantation
title_fullStr Outcomes of a 1-day nonmyeloablative salvage regimen for patients with primary graft failure after allogeneic hematopoietic cell transplantation
title_full_unstemmed Outcomes of a 1-day nonmyeloablative salvage regimen for patients with primary graft failure after allogeneic hematopoietic cell transplantation
title_short Outcomes of a 1-day nonmyeloablative salvage regimen for patients with primary graft failure after allogeneic hematopoietic cell transplantation
title_sort outcomes of a 1-day nonmyeloablative salvage regimen for patients with primary graft failure after allogeneic hematopoietic cell transplantation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214602/
https://www.ncbi.nlm.nih.gov/pubmed/21804612
http://dx.doi.org/10.1038/bmt.2011.158
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