Cariótipo em leucemia mielóide aguda: importância e tipo de alteração em 30 pacientes ao diagnóstico

Detalhes bibliográficos
Autor(a) principal: Pelloso, Luís Arthur Flores
Data de Publicação: 2003
Outros Autores: Chauffaille, Maria de Lourdes Lopes Ferrari [UNIFESP], Ghaname, Fabiana Sinnot, Yamamoto, Mihoko [UNIFESP], Bahia, Daniella Marcia Maranhão [UNIFESP], Kerbauy, José [UNIFESP]
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.
id UFSP_feccde6d965a33cfe50887443a57ec9c
oai_identifier_str oai:repositorio.unifesp.br/:11600/1754
network_acronym_str UFSP
network_name_str Repositório Institucional da UNIFESP
repository_id_str 3465
spelling 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
dc.language.iso.fl_str_mv por
language por
dc.relation.none.fl_str_mv Revista da Associação Médica Brasileira
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv 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
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
_version_ 1814268331849416704