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Outcome of therapy-related myeloid neoplasms treated with azacitidine

BACKGROUND: Therapy-related myeloid neoplasms (t-MN), including myelodysplastic syndromes and acute myeloid leukemia (t-MDS and t-AML) are associated to clinical and biologic unfavorable prognostic features, including high levels of DNA methylation. METHODS: We retrospectively evaluated 50 t-MN pati...

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Autores principales: Fianchi, Luana, Criscuolo, Marianna, Lunghi, Monia, Gaidano, Gianluca, Breccia, Massimo, Levis, Alessandro, Finelli, Carlo, Santini, Valeria, Musto, Pellegrino, Oliva, Esther N, Leoni, Pietro, Aloe Spiriti, Antonietta, D’Alò, Francesco, Hohaus, Stefan, Pagano, Livio, Leone, Giuseppe, Voso, Maria Teresa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3419605/
https://www.ncbi.nlm.nih.gov/pubmed/22853048
http://dx.doi.org/10.1186/1756-8722-5-44
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author Fianchi, Luana
Criscuolo, Marianna
Lunghi, Monia
Gaidano, Gianluca
Breccia, Massimo
Levis, Alessandro
Finelli, Carlo
Santini, Valeria
Musto, Pellegrino
Oliva, Esther N
Leoni, Pietro
Aloe Spiriti, Antonietta
D’Alò, Francesco
Hohaus, Stefan
Pagano, Livio
Leone, Giuseppe
Voso, Maria Teresa
author_facet Fianchi, Luana
Criscuolo, Marianna
Lunghi, Monia
Gaidano, Gianluca
Breccia, Massimo
Levis, Alessandro
Finelli, Carlo
Santini, Valeria
Musto, Pellegrino
Oliva, Esther N
Leoni, Pietro
Aloe Spiriti, Antonietta
D’Alò, Francesco
Hohaus, Stefan
Pagano, Livio
Leone, Giuseppe
Voso, Maria Teresa
author_sort Fianchi, Luana
collection PubMed
description BACKGROUND: Therapy-related myeloid neoplasms (t-MN), including myelodysplastic syndromes and acute myeloid leukemia (t-MDS and t-AML) are associated to clinical and biologic unfavorable prognostic features, including high levels of DNA methylation. METHODS: We retrospectively evaluated 50 t-MN patients (34 MDS and 16 AML) selected among all patients receiving azacitidine (AZA) at 10 Italian Hematology Centers. Patients had developed a t-MN at a median of 6.5 years (range 1.7- 29) after treatment of the primary tumor (hematological neoplasm, 27 patients; solid tumor, 23 patients). RESULTS: The overall response rate was 42% (complete remission: 10 patients, partial remission: 2 and hematological improvement: 8 patients) and was obtained after a median of 3 cycles (range 1–6). Median overall survival (OS) was 21 months (range 1–53.6+) from AZA start. OS was significantly better in patients with less than 20% blasts, in normal karyotype t-AML and when AZA was used as front-line treatment. This was confirmed by the multivariate analysis. CONCLUSIONS: This study reports efficacy of AZA in the largest series of therapy-related MN patients treated with 5-AZA. Our data show that blasts and karyotype maintain their important prognostic role in t-MN also in the azacitidine era.
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spelling pubmed-34196052012-08-16 Outcome of therapy-related myeloid neoplasms treated with azacitidine Fianchi, Luana Criscuolo, Marianna Lunghi, Monia Gaidano, Gianluca Breccia, Massimo Levis, Alessandro Finelli, Carlo Santini, Valeria Musto, Pellegrino Oliva, Esther N Leoni, Pietro Aloe Spiriti, Antonietta D’Alò, Francesco Hohaus, Stefan Pagano, Livio Leone, Giuseppe Voso, Maria Teresa J Hematol Oncol Research BACKGROUND: Therapy-related myeloid neoplasms (t-MN), including myelodysplastic syndromes and acute myeloid leukemia (t-MDS and t-AML) are associated to clinical and biologic unfavorable prognostic features, including high levels of DNA methylation. METHODS: We retrospectively evaluated 50 t-MN patients (34 MDS and 16 AML) selected among all patients receiving azacitidine (AZA) at 10 Italian Hematology Centers. Patients had developed a t-MN at a median of 6.5 years (range 1.7- 29) after treatment of the primary tumor (hematological neoplasm, 27 patients; solid tumor, 23 patients). RESULTS: The overall response rate was 42% (complete remission: 10 patients, partial remission: 2 and hematological improvement: 8 patients) and was obtained after a median of 3 cycles (range 1–6). Median overall survival (OS) was 21 months (range 1–53.6+) from AZA start. OS was significantly better in patients with less than 20% blasts, in normal karyotype t-AML and when AZA was used as front-line treatment. This was confirmed by the multivariate analysis. CONCLUSIONS: This study reports efficacy of AZA in the largest series of therapy-related MN patients treated with 5-AZA. Our data show that blasts and karyotype maintain their important prognostic role in t-MN also in the azacitidine era. BioMed Central 2012-08-01 /pmc/articles/PMC3419605/ /pubmed/22853048 http://dx.doi.org/10.1186/1756-8722-5-44 Text en Copyright ©2012 Fianchi et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Fianchi, Luana
Criscuolo, Marianna
Lunghi, Monia
Gaidano, Gianluca
Breccia, Massimo
Levis, Alessandro
Finelli, Carlo
Santini, Valeria
Musto, Pellegrino
Oliva, Esther N
Leoni, Pietro
Aloe Spiriti, Antonietta
D’Alò, Francesco
Hohaus, Stefan
Pagano, Livio
Leone, Giuseppe
Voso, Maria Teresa
Outcome of therapy-related myeloid neoplasms treated with azacitidine
title Outcome of therapy-related myeloid neoplasms treated with azacitidine
title_full Outcome of therapy-related myeloid neoplasms treated with azacitidine
title_fullStr Outcome of therapy-related myeloid neoplasms treated with azacitidine
title_full_unstemmed Outcome of therapy-related myeloid neoplasms treated with azacitidine
title_short Outcome of therapy-related myeloid neoplasms treated with azacitidine
title_sort outcome of therapy-related myeloid neoplasms treated with azacitidine
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3419605/
https://www.ncbi.nlm.nih.gov/pubmed/22853048
http://dx.doi.org/10.1186/1756-8722-5-44
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