Prognosis for patients with unilateral Wilms' tumor in Rio de Janeiro, Brazil, 1990-2000
Autor(a) principal: | |
---|---|
Data de Publicação: | 2005 |
Outros Autores: | |
Tipo de documento: | Artigo |
Idioma: | por eng |
Título da fonte: | Revista de Saúde Pública |
Texto Completo: | https://www.revistas.usp.br/rsp/article/view/31931 |
Resumo: | OBJECTIVE: To analyze the survival and the main prognostic factors among patients with unilateral Wilms' tumor patients. METHODS: The study cohort included 132 patients with unilateral Wilms' tumor aged under 15 years, who were enrolled in a pediatric oncology service. Survival curves were calculated using the Kaplan-Meier method and the prognostic factors were analyzed using the Cox proportional hazards model. RESULTS: The overall survival rate for five years was 84.6%. The survival probabilities for disease in stages I, II, III and IV stages were: 100%, 94.2%, 83.2% and 31.3%, respectively. The survival rate was 89.4% for patients with favorable histology, 66.7% for focal anaplasia and 40% for diffuse anaplasia. All patients with stage IV disease and diffuse anaplasia died (n=4). All patients with stage I disease, regardless of histology, remained alive at the end of the follow-up period. CONCLUSIONS: Among the variables selected for the final model, only the staging and the histology remained associated with high risk of death risk, while patients aged 24 - 47 months presented better prognosis than the other patients. These results showed the importance of establishing the diagnosis at an early stage, and that the histology is fundamental for guiding the appropriate therapy. |
id |
USP-23_3fcd024c186d3d81a6d12f8400f3cc6a |
---|---|
oai_identifier_str |
oai:revistas.usp.br:article/31931 |
network_acronym_str |
USP-23 |
network_name_str |
Revista de Saúde Pública |
repository_id_str |
|
spelling |
Prognosis for patients with unilateral Wilms' tumor in Rio de Janeiro, Brazil, 1990-2000 Prognóstico de pacientes com tumor de Wilms unilateral no Rio de Janeiro, 1990-2000 Tumor de WilmsNefroblastoma^i1^sdiagnóstNefroblastoma^i1^spatoloPrognósticoAnaplasiaAnálise de sobrevivênciaWilms tumorNephroblastoma^i2^sdiagnoNephroblastoma^i2^spatholPrognosisAnaplasiaSurvival analysis OBJECTIVE: To analyze the survival and the main prognostic factors among patients with unilateral Wilms' tumor patients. METHODS: The study cohort included 132 patients with unilateral Wilms' tumor aged under 15 years, who were enrolled in a pediatric oncology service. Survival curves were calculated using the Kaplan-Meier method and the prognostic factors were analyzed using the Cox proportional hazards model. RESULTS: The overall survival rate for five years was 84.6%. The survival probabilities for disease in stages I, II, III and IV stages were: 100%, 94.2%, 83.2% and 31.3%, respectively. The survival rate was 89.4% for patients with favorable histology, 66.7% for focal anaplasia and 40% for diffuse anaplasia. All patients with stage IV disease and diffuse anaplasia died (n=4). All patients with stage I disease, regardless of histology, remained alive at the end of the follow-up period. CONCLUSIONS: Among the variables selected for the final model, only the staging and the histology remained associated with high risk of death risk, while patients aged 24 - 47 months presented better prognosis than the other patients. These results showed the importance of establishing the diagnosis at an early stage, and that the histology is fundamental for guiding the appropriate therapy. OBJETIVO: Analisar a sobrevida e os principais fatores prognósticos entre os pacientes com tumor de Wilms unilateral. MÉTODOS: A coorte de estudo incluiu 132 casos de tumor de Wilms unilateral em menores de 15 anos de idade matriculados em serviço de oncologia pediátrica, de janeiro de 1990 a dezembro de 2000. Curvas de sobrevida foram confeccionadas utilizando-se o método de Kaplan-Meier e fatores prognósticos foram analisados pelo modelo de riscos proporcionais de Cox. RESULTADOS: A estimativa de sobrevida global em cinco anos foi 84,6%. As probabilidades de sobrevida para os estádios I, II, III e IV foram de 100%; 94,2%; 83,2% e 31,3%, respectivamente. A taxa de sobrevida para os pacientes com: histologia favorável foi de 89,4%, para aqueles com anaplasia focal 66,7 % e com anaplasia difusa 40%. Todos os pacientes com doença em estádio IV e anaplasia difusa foram a óbito (n=4). Todos os pacientes com doença em estádio I, independente da histologia, permaneceram vivos até o final do período de seguimento. CONCLUSÕES: Entre as variáveis escolhidas para o modelo final apenas o estadiamento e a histologia permaneceram associados ao elevado risco de óbito enquanto que os casos na faixa etária entre 24 e 47 meses apresentaram melhor prognóstico que os demais. Esses resultados mostram a importância do diagnóstico em fases iniciais da doença e que a histologia é fundamental para orientar a terapia adequada. Universidade de São Paulo. Faculdade de Saúde Pública2005-10-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionapplication/pdfapplication/pdfhttps://www.revistas.usp.br/rsp/article/view/3193110.1590/S0034-89102005000500006Revista de Saúde Pública; Vol. 39 No. 5 (2005); 731-737 Revista de Saúde Pública; Vol. 39 Núm. 5 (2005); 731-737 Revista de Saúde Pública; v. 39 n. 5 (2005); 731-737 1518-87870034-8910reponame:Revista de Saúde Públicainstname:Universidade de São Paulo (USP)instacron:USPporenghttps://www.revistas.usp.br/rsp/article/view/31931/33919https://www.revistas.usp.br/rsp/article/view/31931/33920Copyright (c) 2017 Revista de Saúde Públicainfo:eu-repo/semantics/openAccessGrabois, Marilia FornaciariMendonça, Gulnar Azevedo e Silva2012-07-08T22:46:10Zoai:revistas.usp.br:article/31931Revistahttps://www.revistas.usp.br/rsp/indexONGhttps://www.revistas.usp.br/rsp/oairevsp@org.usp.br||revsp1@usp.br1518-87870034-8910opendoar:2012-07-08T22:46:10Revista de Saúde Pública - Universidade de São Paulo (USP)false |
dc.title.none.fl_str_mv |
Prognosis for patients with unilateral Wilms' tumor in Rio de Janeiro, Brazil, 1990-2000 Prognóstico de pacientes com tumor de Wilms unilateral no Rio de Janeiro, 1990-2000 |
title |
Prognosis for patients with unilateral Wilms' tumor in Rio de Janeiro, Brazil, 1990-2000 |
spellingShingle |
Prognosis for patients with unilateral Wilms' tumor in Rio de Janeiro, Brazil, 1990-2000 Grabois, Marilia Fornaciari Tumor de Wilms Nefroblastoma^i1^sdiagnóst Nefroblastoma^i1^spatolo Prognóstico Anaplasia Análise de sobrevivência Wilms tumor Nephroblastoma^i2^sdiagno Nephroblastoma^i2^spathol Prognosis Anaplasia Survival analysis |
title_short |
Prognosis for patients with unilateral Wilms' tumor in Rio de Janeiro, Brazil, 1990-2000 |
title_full |
Prognosis for patients with unilateral Wilms' tumor in Rio de Janeiro, Brazil, 1990-2000 |
title_fullStr |
Prognosis for patients with unilateral Wilms' tumor in Rio de Janeiro, Brazil, 1990-2000 |
title_full_unstemmed |
Prognosis for patients with unilateral Wilms' tumor in Rio de Janeiro, Brazil, 1990-2000 |
title_sort |
Prognosis for patients with unilateral Wilms' tumor in Rio de Janeiro, Brazil, 1990-2000 |
author |
Grabois, Marilia Fornaciari |
author_facet |
Grabois, Marilia Fornaciari Mendonça, Gulnar Azevedo e Silva |
author_role |
author |
author2 |
Mendonça, Gulnar Azevedo e Silva |
author2_role |
author |
dc.contributor.author.fl_str_mv |
Grabois, Marilia Fornaciari Mendonça, Gulnar Azevedo e Silva |
dc.subject.por.fl_str_mv |
Tumor de Wilms Nefroblastoma^i1^sdiagnóst Nefroblastoma^i1^spatolo Prognóstico Anaplasia Análise de sobrevivência Wilms tumor Nephroblastoma^i2^sdiagno Nephroblastoma^i2^spathol Prognosis Anaplasia Survival analysis |
topic |
Tumor de Wilms Nefroblastoma^i1^sdiagnóst Nefroblastoma^i1^spatolo Prognóstico Anaplasia Análise de sobrevivência Wilms tumor Nephroblastoma^i2^sdiagno Nephroblastoma^i2^spathol Prognosis Anaplasia Survival analysis |
description |
OBJECTIVE: To analyze the survival and the main prognostic factors among patients with unilateral Wilms' tumor patients. METHODS: The study cohort included 132 patients with unilateral Wilms' tumor aged under 15 years, who were enrolled in a pediatric oncology service. Survival curves were calculated using the Kaplan-Meier method and the prognostic factors were analyzed using the Cox proportional hazards model. RESULTS: The overall survival rate for five years was 84.6%. The survival probabilities for disease in stages I, II, III and IV stages were: 100%, 94.2%, 83.2% and 31.3%, respectively. The survival rate was 89.4% for patients with favorable histology, 66.7% for focal anaplasia and 40% for diffuse anaplasia. All patients with stage IV disease and diffuse anaplasia died (n=4). All patients with stage I disease, regardless of histology, remained alive at the end of the follow-up period. CONCLUSIONS: Among the variables selected for the final model, only the staging and the histology remained associated with high risk of death risk, while patients aged 24 - 47 months presented better prognosis than the other patients. These results showed the importance of establishing the diagnosis at an early stage, and that the histology is fundamental for guiding the appropriate therapy. |
publishDate |
2005 |
dc.date.none.fl_str_mv |
2005-10-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://www.revistas.usp.br/rsp/article/view/31931 10.1590/S0034-89102005000500006 |
url |
https://www.revistas.usp.br/rsp/article/view/31931 |
identifier_str_mv |
10.1590/S0034-89102005000500006 |
dc.language.iso.fl_str_mv |
por eng |
language |
por eng |
dc.relation.none.fl_str_mv |
https://www.revistas.usp.br/rsp/article/view/31931/33919 https://www.revistas.usp.br/rsp/article/view/31931/33920 |
dc.rights.driver.fl_str_mv |
Copyright (c) 2017 Revista de Saúde Pública info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Copyright (c) 2017 Revista de Saúde Pública |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Saúde Pública |
publisher.none.fl_str_mv |
Universidade de São Paulo. Faculdade de Saúde Pública |
dc.source.none.fl_str_mv |
Revista de Saúde Pública; Vol. 39 No. 5 (2005); 731-737 Revista de Saúde Pública; Vol. 39 Núm. 5 (2005); 731-737 Revista de Saúde Pública; v. 39 n. 5 (2005); 731-737 1518-8787 0034-8910 reponame:Revista de Saúde Pública instname:Universidade de São Paulo (USP) instacron:USP |
instname_str |
Universidade de São Paulo (USP) |
instacron_str |
USP |
institution |
USP |
reponame_str |
Revista de Saúde Pública |
collection |
Revista de Saúde Pública |
repository.name.fl_str_mv |
Revista de Saúde Pública - Universidade de São Paulo (USP) |
repository.mail.fl_str_mv |
revsp@org.usp.br||revsp1@usp.br |
_version_ |
1800221783743266816 |