Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnóstico
Autor(a) principal: | |
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Data de Publicação: | 2003 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1590/S0104-42302003000200032 http://repositorio.unifesp.br/handle/11600/1754 |
Resumo: | INTRODUCTION: Cytogenetics in AML at diagnosis is a well defined prognostic tool. Objective: The authors analized karyotype (KT) and clinical data of newly diagnosed AML patients. METHODS: Thirty patients were studied, 16 male and 14 female. Age ranged from 19 to 84 years. Diagnostic criteria were based on WHO classification, immunophenotyping and G banding cytogenetics. They were treated according to standard protocol (daunorrubicin and cytarabine - 3+7) and those who had Acute Promyelocytic Leukemia additionally received ATRA. RESULTS: KT success rate was 84%. According to KT patients were divided into 4 groups: favourable prognosis (FP) (6) (t(8;21), t(15;17)); intermediary prognosis (IP) (7)(four normal karyotypes, + 8, t(1;2) and del 18(q)); unfavourable prognosis (UP); and 3 secondary AML; two evolving from prior Mylelodysplastic Syndrome and one presenting as an initial blast crisis of chronic myeloid leukemia.The median age of FP was 23 years while UP was 60 years (p<0.003).In the FP, 5/6 (83%) achieved complete remission (CR) while only 1/7 (20%)in the IP and 1/8 (12,5%) in the UP. There was a tendency of higher leukocyte count in the unfavourable group. CONCLUSIONS: The rate of karyotype aberrations in AML was 80% and in accordance to literature data (65-95%).There was a clear difference in CR rates between favourable and unfavourable prognosis group. |
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Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnósticoKaryotype in acute myeloid leukemia: importance and type of aberrations in 30 patients at diagnosisAcute Myeloid LeukemiaKaryotypeINTRODUCTION: Cytogenetics in AML at diagnosis is a well defined prognostic tool. Objective: The authors analized karyotype (KT) and clinical data of newly diagnosed AML patients. METHODS: Thirty patients were studied, 16 male and 14 female. Age ranged from 19 to 84 years. Diagnostic criteria were based on WHO classification, immunophenotyping and G banding cytogenetics. They were treated according to standard protocol (daunorrubicin and cytarabine - 3+7) and those who had Acute Promyelocytic Leukemia additionally received ATRA. RESULTS: KT success rate was 84%. According to KT patients were divided into 4 groups: favourable prognosis (FP) (6) (t(8;21), t(15;17)); intermediary prognosis (IP) (7)(four normal karyotypes, + 8, t(1;2) and del 18(q)); unfavourable prognosis (UP); and 3 secondary AML; two evolving from prior Mylelodysplastic Syndrome and one presenting as an initial blast crisis of chronic myeloid leukemia.The median age of FP was 23 years while UP was 60 years (p<0.003).In the FP, 5/6 (83%) achieved complete remission (CR) while only 1/7 (20%)in the IP and 1/8 (12,5%) in the UP. There was a tendency of higher leukocyte count in the unfavourable group. CONCLUSIONS: The rate of karyotype aberrations in AML was 80% and in accordance to literature data (65-95%).There was a clear difference in CR rates between favourable and unfavourable prognosis group.OBJETIVO: Análise sob o ponto de vista citogenético e clínico de pacientes com LMA. MÉTODOS: Foram estudados 30 pacientes, sendo 16 homens e 14 mulheres. A idade variou de 19 a 84 anos. O diagnóstico baseou-se na classificação OMS, imunofenotipagem e citogenética clássica por banda G. Foram tratados com o protocolo daunorrubicina e citarabina (3+7), com adição de ATRA na Leucemia Promielocítica Aguda. RESULTADOS: A taxa de sucesso de cariótipo foi 84%. De acordo com o cariótipo, os pacientes foram divididos em quatro grupos: prognóstico favorável (PF) (6) (t(8;21), t(15;17)); intermediário (PI) (7) (quatro casos com cariótipo normal,+ 8, t(1;2) e del 18(q)); desfavorável (PD) (10) e três casos eram LMA secundária (dois evoluídos de síndrome mielodisplásica e uma apresentação de LMC em crise blástica. No grupo de PF, a idade mediana foi 23 e no PD 60 anos(p<0,003). No grupo PF, 5/6 pacientes (83%) entraram em remissão completa (RC), no PI 1/7 (20%) e no PD 1/8 (12,5%). Houve tendência à leucometria mais elevada no grupo de PD. CONCLUSÕES: A porcentagem de cariótipo alterado em LMA (80%) está dentro dos valores relatados pela literatura (65%-95%). Ficou nítida a diferença entre a taxa de RC do grupo PF versus PD, confirmando a importância do cariótipo na diferenciação dos grupos de risco.Universidade Federal de São Paulo (UNIFESP) Escola Paulista de MedicinaUNIFESP, EPMSciELOAssociação Médica BrasileiraUniversidade Federal de São Paulo (UNIFESP)Pelloso, Luís Arthur FloresChauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP]Ghaname, Fabiana SinnotYamamoto, Mihoko [UNIFESP]Bahia, Daniella Marcia Maranhão [UNIFESP]Kerbauy, José [UNIFESP]2015-06-14T13:30:03Z2015-06-14T13:30:03Z2003-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion150-155application/pdfhttp://dx.doi.org/10.1590/S0104-42302003000200032Revista da Associação Médica Brasileira. Associação Médica Brasileira, v. 49, n. 2, p. 150-155, 2003.10.1590/S0104-42302003000200032S0104-42302003000200032.pdf0104-4230S0104-42302003000200032http://repositorio.unifesp.br/handle/11600/1754porRevista da Associação Médica Brasileirainfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-29T22:08:01Zoai:repositorio.unifesp.br/:11600/1754Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-29T22:08:01Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnóstico Karyotype in acute myeloid leukemia: importance and type of aberrations in 30 patients at diagnosis |
title |
Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnóstico |
spellingShingle |
Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnóstico Pelloso, Luís Arthur Flores Acute Myeloid Leukemia Karyotype |
title_short |
Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnóstico |
title_full |
Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnóstico |
title_fullStr |
Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnóstico |
title_full_unstemmed |
Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnóstico |
title_sort |
Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnóstico |
author |
Pelloso, Luís Arthur Flores |
author_facet |
Pelloso, Luís Arthur Flores Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP] Ghaname, Fabiana Sinnot Yamamoto, Mihoko [UNIFESP] Bahia, Daniella Marcia Maranhão [UNIFESP] Kerbauy, José [UNIFESP] |
author_role |
author |
author2 |
Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP] Ghaname, Fabiana Sinnot Yamamoto, Mihoko [UNIFESP] Bahia, Daniella Marcia Maranhão [UNIFESP] Kerbauy, José [UNIFESP] |
author2_role |
author author author author author |
dc.contributor.none.fl_str_mv |
Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Pelloso, Luís Arthur Flores Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP] Ghaname, Fabiana Sinnot Yamamoto, Mihoko [UNIFESP] Bahia, Daniella Marcia Maranhão [UNIFESP] Kerbauy, José [UNIFESP] |
dc.subject.por.fl_str_mv |
Acute Myeloid Leukemia Karyotype |
topic |
Acute Myeloid Leukemia Karyotype |
description |
INTRODUCTION: Cytogenetics in AML at diagnosis is a well defined prognostic tool. Objective: The authors analized karyotype (KT) and clinical data of newly diagnosed AML patients. METHODS: Thirty patients were studied, 16 male and 14 female. Age ranged from 19 to 84 years. Diagnostic criteria were based on WHO classification, immunophenotyping and G banding cytogenetics. They were treated according to standard protocol (daunorrubicin and cytarabine - 3+7) and those who had Acute Promyelocytic Leukemia additionally received ATRA. RESULTS: KT success rate was 84%. According to KT patients were divided into 4 groups: favourable prognosis (FP) (6) (t(8;21), t(15;17)); intermediary prognosis (IP) (7)(four normal karyotypes, + 8, t(1;2) and del 18(q)); unfavourable prognosis (UP); and 3 secondary AML; two evolving from prior Mylelodysplastic Syndrome and one presenting as an initial blast crisis of chronic myeloid leukemia.The median age of FP was 23 years while UP was 60 years (p<0.003).In the FP, 5/6 (83%) achieved complete remission (CR) while only 1/7 (20%)in the IP and 1/8 (12,5%) in the UP. There was a tendency of higher leukocyte count in the unfavourable group. CONCLUSIONS: The rate of karyotype aberrations in AML was 80% and in accordance to literature data (65-95%).There was a clear difference in CR rates between favourable and unfavourable prognosis group. |
publishDate |
2003 |
dc.date.none.fl_str_mv |
2003-06-01 2015-06-14T13:30:03Z 2015-06-14T13:30:03Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1590/S0104-42302003000200032 Revista da Associação Médica Brasileira. Associação Médica Brasileira, v. 49, n. 2, p. 150-155, 2003. 10.1590/S0104-42302003000200032 S0104-42302003000200032.pdf 0104-4230 S0104-42302003000200032 http://repositorio.unifesp.br/handle/11600/1754 |
url |
http://dx.doi.org/10.1590/S0104-42302003000200032 http://repositorio.unifesp.br/handle/11600/1754 |
identifier_str_mv |
Revista da Associação Médica Brasileira. Associação Médica Brasileira, v. 49, n. 2, p. 150-155, 2003. 10.1590/S0104-42302003000200032 S0104-42302003000200032.pdf 0104-4230 S0104-42302003000200032 |
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por |
language |
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Revista da Associação Médica Brasileira |
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info:eu-repo/semantics/openAccess |
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openAccess |
dc.format.none.fl_str_mv |
150-155 application/pdf |
dc.publisher.none.fl_str_mv |
Associação Médica Brasileira |
publisher.none.fl_str_mv |
Associação Médica Brasileira |
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reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
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Universidade Federal de São Paulo (UNIFESP) |
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UNIFESP |
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UNIFESP |
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Repositório Institucional da UNIFESP |
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Repositório Institucional da UNIFESP |
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Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
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biblioteca.csp@unifesp.br |
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1814268331849416704 |