Aplasia medular adquirida, experiencia en un hospital público de referencia
Background: The first line treatment for patients < 40 years old with aplastic anemia (AA) is allogeneic HLA-identical sibling donor transplantation (SCT). Immunosuppressive therapy (IST) with a combination of Thymoglobuline (ATG) and cyclosporine is used for older patients or those without a do...
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Sociedad Médica de Santiago
2018
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oai:scielo:S0034-988720180002001752018-06-20Aplasia medular adquirida, experiencia en un hospital público de referenciaLeón,PilarCardemil,DanielaOsorio,RocíoPeña,CamilaValladares,XimenaPuga,BárbaraCabrera,María Elena Anemia Aplastic Homologous Immunosuppression Stem Cell Transplantation Transplantation Background: The first line treatment for patients < 40 years old with aplastic anemia (AA) is allogeneic HLA-identical sibling donor transplantation (SCT). Immunosuppressive therapy (IST) with a combination of Thymoglobuline (ATG) and cyclosporine is used for older patients or those without a donor. Five year overall survival (OS) for both therapies is > 70%. Aim: To report the experience with SCT and ATG for AA in a public hospital. Patients and Methods: AA was diagnosed in 42 patients between 1998 and 2016, according to Camitta criteria. Thirty eight (90%) received treatment, 7 (18%) under 40 years old received SCT, and 31 (82%) IST. The rest were not treated. OS was calculated from date of diagnosis until last control, death or loss from follow up. Results: Complete or partial hematologic response, was obtained in 71% and 58% of cases with SCT and IS, respectively. Five year OS was 71% and 55% with SCT and IST, respectively. No difference in response was observed between horse and rabbit ATG. Conclusions: SCT from an HLA-identical sibling donor had a high response rate and survival. IST instead, had a lower response and survival, due to an initial high mortality rate.info:eu-repo/semantics/openAccessSociedad Médica de SantiagoRevista médica de Chile v.146 n.2 20182018-02-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872018000200175es10.4067/s0034-98872018000200175 |
institution |
Scielo Chile |
collection |
Scielo Chile |
language |
Spanish / Castilian |
topic |
Anemia Aplastic Homologous Immunosuppression Stem Cell Transplantation Transplantation |
spellingShingle |
Anemia Aplastic Homologous Immunosuppression Stem Cell Transplantation Transplantation León,Pilar Cardemil,Daniela Osorio,Rocío Peña,Camila Valladares,Ximena Puga,Bárbara Cabrera,María Elena Aplasia medular adquirida, experiencia en un hospital público de referencia |
description |
Background: The first line treatment for patients < 40 years old with aplastic anemia (AA) is allogeneic HLA-identical sibling donor transplantation (SCT). Immunosuppressive therapy (IST) with a combination of Thymoglobuline (ATG) and cyclosporine is used for older patients or those without a donor. Five year overall survival (OS) for both therapies is > 70%. Aim: To report the experience with SCT and ATG for AA in a public hospital. Patients and Methods: AA was diagnosed in 42 patients between 1998 and 2016, according to Camitta criteria. Thirty eight (90%) received treatment, 7 (18%) under 40 years old received SCT, and 31 (82%) IST. The rest were not treated. OS was calculated from date of diagnosis until last control, death or loss from follow up. Results: Complete or partial hematologic response, was obtained in 71% and 58% of cases with SCT and IS, respectively. Five year OS was 71% and 55% with SCT and IST, respectively. No difference in response was observed between horse and rabbit ATG. Conclusions: SCT from an HLA-identical sibling donor had a high response rate and survival. IST instead, had a lower response and survival, due to an initial high mortality rate. |
author |
León,Pilar Cardemil,Daniela Osorio,Rocío Peña,Camila Valladares,Ximena Puga,Bárbara Cabrera,María Elena |
author_facet |
León,Pilar Cardemil,Daniela Osorio,Rocío Peña,Camila Valladares,Ximena Puga,Bárbara Cabrera,María Elena |
author_sort |
León,Pilar |
title |
Aplasia medular adquirida, experiencia en un hospital público de referencia |
title_short |
Aplasia medular adquirida, experiencia en un hospital público de referencia |
title_full |
Aplasia medular adquirida, experiencia en un hospital público de referencia |
title_fullStr |
Aplasia medular adquirida, experiencia en un hospital público de referencia |
title_full_unstemmed |
Aplasia medular adquirida, experiencia en un hospital público de referencia |
title_sort |
aplasia medular adquirida, experiencia en un hospital público de referencia |
publisher |
Sociedad Médica de Santiago |
publishDate |
2018 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0034-98872018000200175 |
work_keys_str_mv |
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