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The expression of CD56 antigen is associated with poor prognosis in patients with acute myeloid leukemia
BACKGROUND: The expression of CD56 is considered a bad prognostic factor for overall survival, lower rates or short complete remission and extramedullary invasion but the results are controversial. The importance of validating new prognostic parameters in acute leukemias was the reason to investigat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Associação Brasileira de Hematologia e Hemoterapia
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415729/ https://www.ncbi.nlm.nih.gov/pubmed/23049296 http://dx.doi.org/10.5581/1516-8484.20110054 |
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author | Alegretti, Ana Paula Bittar, Christina Matzenbacher Bittencourt, Rosane Piccoli, Amanda Kirchner Schneider, Laiana Silla, Lúcia Mariano Bó, Suzane Dal Xavier, Ricardo Machado |
author_facet | Alegretti, Ana Paula Bittar, Christina Matzenbacher Bittencourt, Rosane Piccoli, Amanda Kirchner Schneider, Laiana Silla, Lúcia Mariano Bó, Suzane Dal Xavier, Ricardo Machado |
author_sort | Alegretti, Ana Paula |
collection | PubMed |
description | BACKGROUND: The expression of CD56 is considered a bad prognostic factor for overall survival, lower rates or short complete remission and extramedullary invasion but the results are controversial. The importance of validating new prognostic parameters in acute leukemias was the reason to investigate the CD56 expression in blast cells of patients with acute myeloid leukemia. METHODS: A cohort of 48 patients treated at Hospital de Clinicas de Porto Alegre and diagnosed with acute myeloid leukemia as classified by the French-American-British group (FAB) criteria using cell morphology, cytochemistry and flow cytometry were evaluated. RESULTS: Eight cases (16.7%) were CD56 positive without correlation to age or gender. The highest incidence of CD56 positivity was in FAB subtypes M4 and M5. The death rate during induction was not significantly different between patients with and without CD56 expression (62.5% vs. 27.5%; p-value = 0.097). However, patients that expressed CD56 had significantly lower overall survival than those who did not (mean 4.0 months vs. 14.5 months; p-value = 0.03). CONCLUSIONS: The data suggest that expression of CD56 in acute myeloid leukemia may be indicative of poor prognosis because it is associated with a shorter overall survival. The death rate during induction was not significantly different despite an apparent difference in proportions between groups. |
format | Online Article Text |
id | pubmed-3415729 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Associação Brasileira de Hematologia e Hemoterapia |
record_format | MEDLINE/PubMed |
spelling | pubmed-34157292012-10-04 The expression of CD56 antigen is associated with poor prognosis in patients with acute myeloid leukemia Alegretti, Ana Paula Bittar, Christina Matzenbacher Bittencourt, Rosane Piccoli, Amanda Kirchner Schneider, Laiana Silla, Lúcia Mariano Bó, Suzane Dal Xavier, Ricardo Machado Rev Bras Hematol Hemoter Original Article BACKGROUND: The expression of CD56 is considered a bad prognostic factor for overall survival, lower rates or short complete remission and extramedullary invasion but the results are controversial. The importance of validating new prognostic parameters in acute leukemias was the reason to investigate the CD56 expression in blast cells of patients with acute myeloid leukemia. METHODS: A cohort of 48 patients treated at Hospital de Clinicas de Porto Alegre and diagnosed with acute myeloid leukemia as classified by the French-American-British group (FAB) criteria using cell morphology, cytochemistry and flow cytometry were evaluated. RESULTS: Eight cases (16.7%) were CD56 positive without correlation to age or gender. The highest incidence of CD56 positivity was in FAB subtypes M4 and M5. The death rate during induction was not significantly different between patients with and without CD56 expression (62.5% vs. 27.5%; p-value = 0.097). However, patients that expressed CD56 had significantly lower overall survival than those who did not (mean 4.0 months vs. 14.5 months; p-value = 0.03). CONCLUSIONS: The data suggest that expression of CD56 in acute myeloid leukemia may be indicative of poor prognosis because it is associated with a shorter overall survival. The death rate during induction was not significantly different despite an apparent difference in proportions between groups. Associação Brasileira de Hematologia e Hemoterapia 2011 /pmc/articles/PMC3415729/ /pubmed/23049296 http://dx.doi.org/10.5581/1516-8484.20110054 Text en http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Article Alegretti, Ana Paula Bittar, Christina Matzenbacher Bittencourt, Rosane Piccoli, Amanda Kirchner Schneider, Laiana Silla, Lúcia Mariano Bó, Suzane Dal Xavier, Ricardo Machado The expression of CD56 antigen is associated with poor prognosis in patients with acute myeloid leukemia |
title | The expression of CD56 antigen is associated with poor prognosis in patients with acute myeloid leukemia |
title_full | The expression of CD56 antigen is associated with poor prognosis in patients with acute myeloid leukemia |
title_fullStr | The expression of CD56 antigen is associated with poor prognosis in patients with acute myeloid leukemia |
title_full_unstemmed | The expression of CD56 antigen is associated with poor prognosis in patients with acute myeloid leukemia |
title_short | The expression of CD56 antigen is associated with poor prognosis in patients with acute myeloid leukemia |
title_sort | expression of cd56 antigen is associated with poor prognosis in patients with acute myeloid leukemia |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3415729/ https://www.ncbi.nlm.nih.gov/pubmed/23049296 http://dx.doi.org/10.5581/1516-8484.20110054 |
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