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Outcome of childhood acute lymphoblastic leukemia treatment in a single center in Brazil: A survival analysis study
BACKGROUND: Acute lymphoblastic leukemia (ALL) is the most common neoplasm in childhood. The probability of current overall survival (OS) is around 90% in developed countries. There are few studies that demonstrate the results in Brazil. AIM: This work aims to analyze the results of children with AL...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789616/ https://www.ncbi.nlm.nih.gov/pubmed/34114751 http://dx.doi.org/10.1002/cnr2.1452 |
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author | Bonilha, Thais A. Obadia, Danielle D. A. Valveson, Andressa C. Land, Marcelo G. P. |
author_facet | Bonilha, Thais A. Obadia, Danielle D. A. Valveson, Andressa C. Land, Marcelo G. P. |
author_sort | Bonilha, Thais A. |
collection | PubMed |
description | BACKGROUND: Acute lymphoblastic leukemia (ALL) is the most common neoplasm in childhood. The probability of current overall survival (OS) is around 90% in developed countries. There are few studies that demonstrate the results in Brazil. AIM: This work aims to analyze the results of children with ALL treated at a single institution in Rio de Janeiro. METHODS AND RESULTS: Retrospective analysis survival study of a cohort of childhood ALL patients treated in Hemorio. Kaplan–Meier and log‐rank methods were used for the analysis of OS and events‐free survival (EFS) and the Cox proportional hazards regression model for multivariate analysis. The probability of OS and EFS at 6 years was 52% and 45%. The probability of OS and EFS in 6 years for patients aged 10‐17 years was 31% and 28% and for the younger was 65% and 55%, respectively (p < .001). A probability of OS and EFS in 6 years for patients with more than 100 000 leukocytes/mm(3) at diagnosis was 19% and 16% and those with less than 100 000 were 62% (p = .007) and 55% (p = .008). Those who received less than 10 doses of native Escherichia coli asparaginase had a probability of OS and EFS in 6 years of 27% and 21% and those who received at least 10 doses were 74% and 65% (p < .001). CONCLUSIONS: The presence of a high number of adolescents and high‐risk patients, as well as many patients who discontinued the use of asparaginase or any substitute led to a lower probability of OS and EFS in our cohort. |
format | Online Article Text |
id | pubmed-8789616 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-87896162022-02-01 Outcome of childhood acute lymphoblastic leukemia treatment in a single center in Brazil: A survival analysis study Bonilha, Thais A. Obadia, Danielle D. A. Valveson, Andressa C. Land, Marcelo G. P. Cancer Rep (Hoboken) Clinical Research Article BACKGROUND: Acute lymphoblastic leukemia (ALL) is the most common neoplasm in childhood. The probability of current overall survival (OS) is around 90% in developed countries. There are few studies that demonstrate the results in Brazil. AIM: This work aims to analyze the results of children with ALL treated at a single institution in Rio de Janeiro. METHODS AND RESULTS: Retrospective analysis survival study of a cohort of childhood ALL patients treated in Hemorio. Kaplan–Meier and log‐rank methods were used for the analysis of OS and events‐free survival (EFS) and the Cox proportional hazards regression model for multivariate analysis. The probability of OS and EFS at 6 years was 52% and 45%. The probability of OS and EFS in 6 years for patients aged 10‐17 years was 31% and 28% and for the younger was 65% and 55%, respectively (p < .001). A probability of OS and EFS in 6 years for patients with more than 100 000 leukocytes/mm(3) at diagnosis was 19% and 16% and those with less than 100 000 were 62% (p = .007) and 55% (p = .008). Those who received less than 10 doses of native Escherichia coli asparaginase had a probability of OS and EFS in 6 years of 27% and 21% and those who received at least 10 doses were 74% and 65% (p < .001). CONCLUSIONS: The presence of a high number of adolescents and high‐risk patients, as well as many patients who discontinued the use of asparaginase or any substitute led to a lower probability of OS and EFS in our cohort. John Wiley and Sons Inc. 2021-06-11 /pmc/articles/PMC8789616/ /pubmed/34114751 http://dx.doi.org/10.1002/cnr2.1452 Text en © 2021 The Authors. Cancer Reports published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Clinical Research Article Bonilha, Thais A. Obadia, Danielle D. A. Valveson, Andressa C. Land, Marcelo G. P. Outcome of childhood acute lymphoblastic leukemia treatment in a single center in Brazil: A survival analysis study |
title | Outcome of childhood acute lymphoblastic leukemia treatment in a single center in Brazil: A survival analysis study |
title_full | Outcome of childhood acute lymphoblastic leukemia treatment in a single center in Brazil: A survival analysis study |
title_fullStr | Outcome of childhood acute lymphoblastic leukemia treatment in a single center in Brazil: A survival analysis study |
title_full_unstemmed | Outcome of childhood acute lymphoblastic leukemia treatment in a single center in Brazil: A survival analysis study |
title_short | Outcome of childhood acute lymphoblastic leukemia treatment in a single center in Brazil: A survival analysis study |
title_sort | outcome of childhood acute lymphoblastic leukemia treatment in a single center in brazil: a survival analysis study |
topic | Clinical Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8789616/ https://www.ncbi.nlm.nih.gov/pubmed/34114751 http://dx.doi.org/10.1002/cnr2.1452 |
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