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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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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. |
format | Online Article Text |
id | pubmed-3419605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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