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Molecular characteristics and outcomes in Hispanic and non‐Hispanic patients with acute myeloid leukemia

Hispanic patients have been reported to have an increased incidence of AML and possibly inferior outcomes compared to non‐Hispanics. We conducted a retrospective study of 225 AML patients (58 Hispanic and 167 non‐Hispanic) at two academic medical centers in Florida. Disease characteristics, cytogene...

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Autores principales: Bradley, Terrence, Kwon, Deukwoo, Monge, Jorge, Sekeres, Mikkael, Chandhok, Namrata, Thomassen, Amber, Swords, Ronan, Padron, Eric, Lancet, Jeff, Talati, Chetasi, Watts, Justin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713060/
https://www.ncbi.nlm.nih.gov/pubmed/36467830
http://dx.doi.org/10.1002/jha2.589
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author Bradley, Terrence
Kwon, Deukwoo
Monge, Jorge
Sekeres, Mikkael
Chandhok, Namrata
Thomassen, Amber
Swords, Ronan
Padron, Eric
Lancet, Jeff
Talati, Chetasi
Watts, Justin
author_facet Bradley, Terrence
Kwon, Deukwoo
Monge, Jorge
Sekeres, Mikkael
Chandhok, Namrata
Thomassen, Amber
Swords, Ronan
Padron, Eric
Lancet, Jeff
Talati, Chetasi
Watts, Justin
author_sort Bradley, Terrence
collection PubMed
description Hispanic patients have been reported to have an increased incidence of AML and possibly inferior outcomes compared to non‐Hispanics. We conducted a retrospective study of 225 AML patients (58 Hispanic and 167 non‐Hispanic) at two academic medical centers in Florida. Disease characteristics, cytogenetics, mutation profiles, and clinical outcomes were assessed. Hispanic patients were younger at presentation than non‐Hispanics (p = 0.0013). We found associations between single gene mutations and ethnicity, with IDH1 mutations being more common in non‐Hispanics (95.2% vs. 4.8%, p = 0.0182) and WT1 mutations more common in Hispanics (62.5% vs. 37.5%, p = 0.0455). We also found an emerging trend towards adverse risk cytogenetics in Hispanic patients (p = 0.1796), as well as high risk fusions such as MLL‐r (70% vs. 30%, p = 0.004). There was no difference in overall survival (OS) between Hispanic and non‐Hispanics patients. When examining only newly diagnosed patients (n = 105), there was improved OS in Hispanics (median 44.7 months vs. 14 months, p = 0.026) by univariate analysis and equivalent OS by multivariate analysis (hazard ratio = 1.52 [95% CI = 0.74–3.15]). Hispanics with a driver mutation not class‐defining had improved survival compared to non‐Hispanics. Our study demonstrates significant genetic differences between Floridian Hispanics and non‐Hispanics, but no difference in OS in patients treated at an academic medical center.
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spelling pubmed-97130602022-12-02 Molecular characteristics and outcomes in Hispanic and non‐Hispanic patients with acute myeloid leukemia Bradley, Terrence Kwon, Deukwoo Monge, Jorge Sekeres, Mikkael Chandhok, Namrata Thomassen, Amber Swords, Ronan Padron, Eric Lancet, Jeff Talati, Chetasi Watts, Justin EJHaem Haematologic Malignancy ‐ Myeloid Hispanic patients have been reported to have an increased incidence of AML and possibly inferior outcomes compared to non‐Hispanics. We conducted a retrospective study of 225 AML patients (58 Hispanic and 167 non‐Hispanic) at two academic medical centers in Florida. Disease characteristics, cytogenetics, mutation profiles, and clinical outcomes were assessed. Hispanic patients were younger at presentation than non‐Hispanics (p = 0.0013). We found associations between single gene mutations and ethnicity, with IDH1 mutations being more common in non‐Hispanics (95.2% vs. 4.8%, p = 0.0182) and WT1 mutations more common in Hispanics (62.5% vs. 37.5%, p = 0.0455). We also found an emerging trend towards adverse risk cytogenetics in Hispanic patients (p = 0.1796), as well as high risk fusions such as MLL‐r (70% vs. 30%, p = 0.004). There was no difference in overall survival (OS) between Hispanic and non‐Hispanics patients. When examining only newly diagnosed patients (n = 105), there was improved OS in Hispanics (median 44.7 months vs. 14 months, p = 0.026) by univariate analysis and equivalent OS by multivariate analysis (hazard ratio = 1.52 [95% CI = 0.74–3.15]). Hispanics with a driver mutation not class‐defining had improved survival compared to non‐Hispanics. Our study demonstrates significant genetic differences between Floridian Hispanics and non‐Hispanics, but no difference in OS in patients treated at an academic medical center. John Wiley and Sons Inc. 2022-10-18 /pmc/articles/PMC9713060/ /pubmed/36467830 http://dx.doi.org/10.1002/jha2.589 Text en © 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd. 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 Haematologic Malignancy ‐ Myeloid
Bradley, Terrence
Kwon, Deukwoo
Monge, Jorge
Sekeres, Mikkael
Chandhok, Namrata
Thomassen, Amber
Swords, Ronan
Padron, Eric
Lancet, Jeff
Talati, Chetasi
Watts, Justin
Molecular characteristics and outcomes in Hispanic and non‐Hispanic patients with acute myeloid leukemia
title Molecular characteristics and outcomes in Hispanic and non‐Hispanic patients with acute myeloid leukemia
title_full Molecular characteristics and outcomes in Hispanic and non‐Hispanic patients with acute myeloid leukemia
title_fullStr Molecular characteristics and outcomes in Hispanic and non‐Hispanic patients with acute myeloid leukemia
title_full_unstemmed Molecular characteristics and outcomes in Hispanic and non‐Hispanic patients with acute myeloid leukemia
title_short Molecular characteristics and outcomes in Hispanic and non‐Hispanic patients with acute myeloid leukemia
title_sort molecular characteristics and outcomes in hispanic and non‐hispanic patients with acute myeloid leukemia
topic Haematologic Malignancy ‐ Myeloid
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713060/
https://www.ncbi.nlm.nih.gov/pubmed/36467830
http://dx.doi.org/10.1002/jha2.589
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