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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...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8394759 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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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