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Late chimerical status after bone marrow transplantation in severe aplastic anemia according to two different preparatory regimens

BACKGROUND: This study investigated the influence of two conditioning regimens on the chimerical status of 104 patients with acquired severe aplastic anemia. METHODS: Patients were monitored for at least 18 months after related bone marrow transplantation and reaching partial or complete hematologic...

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Autores principales: Quiroga, Marcia, Pereira, Noemi Farah, Bitencourt, Marco Antonio, Bonfim, Carmem, Monteiro, Marianna Gendre de Mesquita, Pasquini, Ricardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Sociedade Brasileira de Hematologia e Hemoterapia 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001926/
https://www.ncbi.nlm.nih.gov/pubmed/30057984
http://dx.doi.org/10.1016/j.htct.2017.11.011
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author Quiroga, Marcia
Pereira, Noemi Farah
Bitencourt, Marco Antonio
Bonfim, Carmem
Monteiro, Marianna Gendre de Mesquita
Pasquini, Ricardo
author_facet Quiroga, Marcia
Pereira, Noemi Farah
Bitencourt, Marco Antonio
Bonfim, Carmem
Monteiro, Marianna Gendre de Mesquita
Pasquini, Ricardo
author_sort Quiroga, Marcia
collection PubMed
description BACKGROUND: This study investigated the influence of two conditioning regimens on the chimerical status of 104 patients with acquired severe aplastic anemia. METHODS: Patients were monitored for at least 18 months after related bone marrow transplantation and reaching partial or complete hematologic recovery. Group I patients (n = 55) received 200 mg/kg cyclophosphamide alone and Group II (n = 49) received 120 mg/kg cyclophosphamide associated with 12 mg/kg busulfan. Patients were classified in three chimerism levels according to the percentage of donor cells in the peripheral blood. RESULTS: Chimerism ≤50% occurred in 36.4% of Group I and none of Group II; chimerism 51–90% was found in 20.0% of Group I and 10.2% of Group II; and chimerism >90% was found in 43.6% of Group I versus 89.8% of Group II. A significant association (p-value < 0.001) was found between conditioning type and chimerism levels. A higher number of infused cells was associated with higher levels of chimerism only in Group I (p-value = 0.013). Multivariate analysis showed that chimerism >90% is associated with the cyclophosphamide plus busulfan conditioning (p-value < 0.001) and higher number of infused cells (p-value = 0.009), suggesting that these factors are predictive of graft outcome. Regarding hematological recovery, higher chimerism levels were associated with higher neutrophil (p-value = 0.003) and platelet counts (p-value < 0.001) in Group I only. These results show that myeloablative conditioning favors full donor chimerism and non-myeloablative conditioning predisposes to mixed chimerism or autologous recovery of hematopoiesis. CONCLUSION: These data show that autologous recovery depends on the intensity of immunosuppression and that the immunosuppressive function of cyclophosphamide alone can induce this type of hematopoietic recovery.
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spelling pubmed-60019262018-06-15 Late chimerical status after bone marrow transplantation in severe aplastic anemia according to two different preparatory regimens Quiroga, Marcia Pereira, Noemi Farah Bitencourt, Marco Antonio Bonfim, Carmem Monteiro, Marianna Gendre de Mesquita Pasquini, Ricardo Hematol Transfus Cell Ther Original Article BACKGROUND: This study investigated the influence of two conditioning regimens on the chimerical status of 104 patients with acquired severe aplastic anemia. METHODS: Patients were monitored for at least 18 months after related bone marrow transplantation and reaching partial or complete hematologic recovery. Group I patients (n = 55) received 200 mg/kg cyclophosphamide alone and Group II (n = 49) received 120 mg/kg cyclophosphamide associated with 12 mg/kg busulfan. Patients were classified in three chimerism levels according to the percentage of donor cells in the peripheral blood. RESULTS: Chimerism ≤50% occurred in 36.4% of Group I and none of Group II; chimerism 51–90% was found in 20.0% of Group I and 10.2% of Group II; and chimerism >90% was found in 43.6% of Group I versus 89.8% of Group II. A significant association (p-value < 0.001) was found between conditioning type and chimerism levels. A higher number of infused cells was associated with higher levels of chimerism only in Group I (p-value = 0.013). Multivariate analysis showed that chimerism >90% is associated with the cyclophosphamide plus busulfan conditioning (p-value < 0.001) and higher number of infused cells (p-value = 0.009), suggesting that these factors are predictive of graft outcome. Regarding hematological recovery, higher chimerism levels were associated with higher neutrophil (p-value = 0.003) and platelet counts (p-value < 0.001) in Group I only. These results show that myeloablative conditioning favors full donor chimerism and non-myeloablative conditioning predisposes to mixed chimerism or autologous recovery of hematopoiesis. CONCLUSION: These data show that autologous recovery depends on the intensity of immunosuppression and that the immunosuppressive function of cyclophosphamide alone can induce this type of hematopoietic recovery. Sociedade Brasileira de Hematologia e Hemoterapia 2018 2018-02-17 /pmc/articles/PMC6001926/ /pubmed/30057984 http://dx.doi.org/10.1016/j.htct.2017.11.011 Text en © 2018 Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular. Published by Elsevier Editora Ltda. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Quiroga, Marcia
Pereira, Noemi Farah
Bitencourt, Marco Antonio
Bonfim, Carmem
Monteiro, Marianna Gendre de Mesquita
Pasquini, Ricardo
Late chimerical status after bone marrow transplantation in severe aplastic anemia according to two different preparatory regimens
title Late chimerical status after bone marrow transplantation in severe aplastic anemia according to two different preparatory regimens
title_full Late chimerical status after bone marrow transplantation in severe aplastic anemia according to two different preparatory regimens
title_fullStr Late chimerical status after bone marrow transplantation in severe aplastic anemia according to two different preparatory regimens
title_full_unstemmed Late chimerical status after bone marrow transplantation in severe aplastic anemia according to two different preparatory regimens
title_short Late chimerical status after bone marrow transplantation in severe aplastic anemia according to two different preparatory regimens
title_sort late chimerical status after bone marrow transplantation in severe aplastic anemia according to two different preparatory regimens
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6001926/
https://www.ncbi.nlm.nih.gov/pubmed/30057984
http://dx.doi.org/10.1016/j.htct.2017.11.011
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