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Hypomethylating Agents (HMAs) as Salvage Therapy in Relapsed or Refractory AML: An Italian Multicentric Retrospective Study

Data on the use of azacytidine and decitabine as salvage therapy for acute myeloid leukemia are limited. We retrospectively reviewed clinical records of 100 patients treated with hypomethylating agents (HMA) as salvage therapy in nine Italian institutions. A total of 24% of patients obtained a respo...

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Autores principales: Lessi, Federica, Laurino, Marica, Papayannidis, Cristina, Vitagliano, Orsola, Grimaldi, Francesco, Lazzarotto, Davide, Gottardi, Michele, Crisà, Elena, Riva, Marta, Reda, Gianluigi, Ermani, Mario, Semenzato, Gianpietro, Trentin, Livio, Ferrara, Felicetto
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394759/
https://www.ncbi.nlm.nih.gov/pubmed/34440176
http://dx.doi.org/10.3390/biomedicines9080972
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author Lessi, Federica
Laurino, Marica
Papayannidis, Cristina
Vitagliano, Orsola
Grimaldi, Francesco
Lazzarotto, Davide
Gottardi, Michele
Crisà, Elena
Riva, Marta
Reda, Gianluigi
Ermani, Mario
Semenzato, Gianpietro
Trentin, Livio
Ferrara, Felicetto
author_facet Lessi, Federica
Laurino, Marica
Papayannidis, Cristina
Vitagliano, Orsola
Grimaldi, Francesco
Lazzarotto, Davide
Gottardi, Michele
Crisà, Elena
Riva, Marta
Reda, Gianluigi
Ermani, Mario
Semenzato, Gianpietro
Trentin, Livio
Ferrara, Felicetto
author_sort Lessi, Federica
collection PubMed
description Data on the use of azacytidine and decitabine as salvage therapy for acute myeloid leukemia are limited. We retrospectively reviewed clinical records of 100 patients treated with hypomethylating agents (HMA) as salvage therapy in nine Italian institutions. A total of 24% of patients obtained a response to HMA (CR, PR, or CRi), while 26% showed a stable disease (SD); 50% of patients experienced progressive disease. Median OS was 6.5 months. OS in patients with de novo AML was 6.1 months, while OS in patients with secondary AML (sAML) was 12.3 months (p = 0.037). Median OS after HMA in patients with SD as best response to HMA was similar to median OS in patients with response to HMA (10.6 months vs. 13 months). On multivariate analysis, OS difference between patients who obtained a response versus patients who did not was significant (p = 0.0037). OS difference in sAML was significantly better than in de novo AML (p < 0.00001). HMA showed a remarkable efficacy in terms of response rate and OS in a subgroup of patients (sAMLs), historically characterized by a poor outcome. Therefore, 5Azacitidine and decitabine may represent a good clinical option in a selected patient population with relapsed or refractory AML, unsuitable for allo-HSCT.
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spelling pubmed-83947592021-08-28 Hypomethylating Agents (HMAs) as Salvage Therapy in Relapsed or Refractory AML: An Italian Multicentric Retrospective Study Lessi, Federica Laurino, Marica Papayannidis, Cristina Vitagliano, Orsola Grimaldi, Francesco Lazzarotto, Davide Gottardi, Michele Crisà, Elena Riva, Marta Reda, Gianluigi Ermani, Mario Semenzato, Gianpietro Trentin, Livio Ferrara, Felicetto Biomedicines Article Data on the use of azacytidine and decitabine as salvage therapy for acute myeloid leukemia are limited. We retrospectively reviewed clinical records of 100 patients treated with hypomethylating agents (HMA) as salvage therapy in nine Italian institutions. A total of 24% of patients obtained a response to HMA (CR, PR, or CRi), while 26% showed a stable disease (SD); 50% of patients experienced progressive disease. Median OS was 6.5 months. OS in patients with de novo AML was 6.1 months, while OS in patients with secondary AML (sAML) was 12.3 months (p = 0.037). Median OS after HMA in patients with SD as best response to HMA was similar to median OS in patients with response to HMA (10.6 months vs. 13 months). On multivariate analysis, OS difference between patients who obtained a response versus patients who did not was significant (p = 0.0037). OS difference in sAML was significantly better than in de novo AML (p < 0.00001). HMA showed a remarkable efficacy in terms of response rate and OS in a subgroup of patients (sAMLs), historically characterized by a poor outcome. Therefore, 5Azacitidine and decitabine may represent a good clinical option in a selected patient population with relapsed or refractory AML, unsuitable for allo-HSCT. MDPI 2021-08-06 /pmc/articles/PMC8394759/ /pubmed/34440176 http://dx.doi.org/10.3390/biomedicines9080972 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lessi, Federica
Laurino, Marica
Papayannidis, Cristina
Vitagliano, Orsola
Grimaldi, Francesco
Lazzarotto, Davide
Gottardi, Michele
Crisà, Elena
Riva, Marta
Reda, Gianluigi
Ermani, Mario
Semenzato, Gianpietro
Trentin, Livio
Ferrara, Felicetto
Hypomethylating Agents (HMAs) as Salvage Therapy in Relapsed or Refractory AML: An Italian Multicentric Retrospective Study
title Hypomethylating Agents (HMAs) as Salvage Therapy in Relapsed or Refractory AML: An Italian Multicentric Retrospective Study
title_full Hypomethylating Agents (HMAs) as Salvage Therapy in Relapsed or Refractory AML: An Italian Multicentric Retrospective Study
title_fullStr Hypomethylating Agents (HMAs) as Salvage Therapy in Relapsed or Refractory AML: An Italian Multicentric Retrospective Study
title_full_unstemmed Hypomethylating Agents (HMAs) as Salvage Therapy in Relapsed or Refractory AML: An Italian Multicentric Retrospective Study
title_short Hypomethylating Agents (HMAs) as Salvage Therapy in Relapsed or Refractory AML: An Italian Multicentric Retrospective Study
title_sort hypomethylating agents (hmas) as salvage therapy in relapsed or refractory aml: an italian multicentric retrospective study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8394759/
https://www.ncbi.nlm.nih.gov/pubmed/34440176
http://dx.doi.org/10.3390/biomedicines9080972
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