Hematopoietic stem cell transplantation in the treatment of multiple myeloma

Detalhes bibliográficos
Autor(a) principal: Maiolino,Angelo
Data de Publicação: 2002
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Revista brasileira de hematologia e hemoterapia (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842002000300005
Resumo: Multiple myeloma is a malignant clonal plasma cell disorder that accounts for about 10% of all hematological malignancies. Conventional melphalan-based chemotherapy produces less than 5% of complete remission rates, with less than 5% of patients surviving 10 years or more. The VAD regimen is very effective to induce cytoreduction, but does not prolong event free survival or overall survival. High-dose therapy with autologous bone marrow or peripheral blood stem cell support induces complete remission in 30%-50% of patients, with a very low transplant related mortality (<5%). Both event free survival and overall survival are prolonged with High-dose therapy, but relapses continue to be a major problem. A subset of patients (chromosome 13 abnormalities and high level of beta2-microglobulin at diagnosis) at high risk of relapse has been identified. Double transplants and post-transplant strategies, with the use of alpha interferon, thalidomide, or combined chemotherapy, are additional measures used to reduce the incidence of relapse. Allogeneic transplants can induce durable molecular remissions. However, the very high (30%-50%) transplant-related mortality limits the application of this procedure. The emerging concept of non-myeloablative transplants may be a very attractive alternative to improve these results. This strategy may be associated with lower transplant related mortality, and yet provide a graft versus myeloma effect, potentially increasing event free survival and overall survival.
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spelling Hematopoietic stem cell transplantation in the treatment of multiple myelomaMultiple myelomahematopoietic stem cell transplantationMultiple myeloma is a malignant clonal plasma cell disorder that accounts for about 10% of all hematological malignancies. Conventional melphalan-based chemotherapy produces less than 5% of complete remission rates, with less than 5% of patients surviving 10 years or more. The VAD regimen is very effective to induce cytoreduction, but does not prolong event free survival or overall survival. High-dose therapy with autologous bone marrow or peripheral blood stem cell support induces complete remission in 30%-50% of patients, with a very low transplant related mortality (<5%). Both event free survival and overall survival are prolonged with High-dose therapy, but relapses continue to be a major problem. A subset of patients (chromosome 13 abnormalities and high level of beta2-microglobulin at diagnosis) at high risk of relapse has been identified. Double transplants and post-transplant strategies, with the use of alpha interferon, thalidomide, or combined chemotherapy, are additional measures used to reduce the incidence of relapse. Allogeneic transplants can induce durable molecular remissions. However, the very high (30%-50%) transplant-related mortality limits the application of this procedure. The emerging concept of non-myeloablative transplants may be a very attractive alternative to improve these results. This strategy may be associated with lower transplant related mortality, and yet provide a graft versus myeloma effect, potentially increasing event free survival and overall survival.Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular2002-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842002000300005Revista Brasileira de Hematologia e Hemoterapia v.24 n.3 2002reponame:Revista brasileira de hematologia e hemoterapia (Online)instname:Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)instacron:ABHHTC10.1590/S1516-84842002000300005info:eu-repo/semantics/openAccessMaiolino,Angeloeng2003-01-14T00:00:00Zoai:scielo:S1516-84842002000300005Revistahttp://www.rbhh.org/pt/archivo/https://old.scielo.br/oai/scielo-oai.phpsbhh@terra.com.br||secretaria@rbhh.org1806-08701516-8484opendoar:2003-01-14T00:00Revista brasileira de hematologia e hemoterapia (Online) - Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)false
dc.title.none.fl_str_mv Hematopoietic stem cell transplantation in the treatment of multiple myeloma
title Hematopoietic stem cell transplantation in the treatment of multiple myeloma
spellingShingle Hematopoietic stem cell transplantation in the treatment of multiple myeloma
Maiolino,Angelo
Multiple myeloma
hematopoietic stem cell transplantation
title_short Hematopoietic stem cell transplantation in the treatment of multiple myeloma
title_full Hematopoietic stem cell transplantation in the treatment of multiple myeloma
title_fullStr Hematopoietic stem cell transplantation in the treatment of multiple myeloma
title_full_unstemmed Hematopoietic stem cell transplantation in the treatment of multiple myeloma
title_sort Hematopoietic stem cell transplantation in the treatment of multiple myeloma
author Maiolino,Angelo
author_facet Maiolino,Angelo
author_role author
dc.contributor.author.fl_str_mv Maiolino,Angelo
dc.subject.por.fl_str_mv Multiple myeloma
hematopoietic stem cell transplantation
topic Multiple myeloma
hematopoietic stem cell transplantation
description Multiple myeloma is a malignant clonal plasma cell disorder that accounts for about 10% of all hematological malignancies. Conventional melphalan-based chemotherapy produces less than 5% of complete remission rates, with less than 5% of patients surviving 10 years or more. The VAD regimen is very effective to induce cytoreduction, but does not prolong event free survival or overall survival. High-dose therapy with autologous bone marrow or peripheral blood stem cell support induces complete remission in 30%-50% of patients, with a very low transplant related mortality (<5%). Both event free survival and overall survival are prolonged with High-dose therapy, but relapses continue to be a major problem. A subset of patients (chromosome 13 abnormalities and high level of beta2-microglobulin at diagnosis) at high risk of relapse has been identified. Double transplants and post-transplant strategies, with the use of alpha interferon, thalidomide, or combined chemotherapy, are additional measures used to reduce the incidence of relapse. Allogeneic transplants can induce durable molecular remissions. However, the very high (30%-50%) transplant-related mortality limits the application of this procedure. The emerging concept of non-myeloablative transplants may be a very attractive alternative to improve these results. This strategy may be associated with lower transplant related mortality, and yet provide a graft versus myeloma effect, potentially increasing event free survival and overall survival.
publishDate 2002
dc.date.none.fl_str_mv 2002-01-01
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842002000300005
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dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S1516-84842002000300005
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dc.publisher.none.fl_str_mv Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular
publisher.none.fl_str_mv Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular
dc.source.none.fl_str_mv Revista Brasileira de Hematologia e Hemoterapia v.24 n.3 2002
reponame:Revista brasileira de hematologia e hemoterapia (Online)
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reponame_str Revista brasileira de hematologia e hemoterapia (Online)
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repository.name.fl_str_mv Revista brasileira de hematologia e hemoterapia (Online) - Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
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