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Real Life Use of Bendamustine in Elderly Patients with Lymphoid Neoplasia
Background. Bendamustine is a cytotoxic alkylating drug with a broad range of indications as a single agent or in combination therapy in lymphoid neoplasia patients. However, its tolerability in elderly patients is still debated. Methods: An observational, retrospective study was carried out; patien...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066290/ https://www.ncbi.nlm.nih.gov/pubmed/33808164 http://dx.doi.org/10.3390/jpm11040249 |
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author | Dogliotti, Irene Ragaini, Simone Vassallo, Francesco Boccellato, Elia De Luca, Gabriele Perutelli, Francesca Boccomini, Carola Clerico, Michele Botto, Barbara Grimaldi, Daniele Orsucci, Lorella Ferrero, Simone Vitale, Candida Ferrero, Dario Coscia, Marta Cavallo, Federica |
author_facet | Dogliotti, Irene Ragaini, Simone Vassallo, Francesco Boccellato, Elia De Luca, Gabriele Perutelli, Francesca Boccomini, Carola Clerico, Michele Botto, Barbara Grimaldi, Daniele Orsucci, Lorella Ferrero, Simone Vitale, Candida Ferrero, Dario Coscia, Marta Cavallo, Federica |
author_sort | Dogliotti, Irene |
collection | PubMed |
description | Background. Bendamustine is a cytotoxic alkylating drug with a broad range of indications as a single agent or in combination therapy in lymphoid neoplasia patients. However, its tolerability in elderly patients is still debated. Methods: An observational, retrospective study was carried out; patients with chronic lymphocytic leukemia (CLL) or lymphoma, aged ≥ 65 years old, treated with bendamustine-based regimens in first or subsequent lines between 2010 and 2020 were considered eligible. Results: Overall, 179 patients aged ≥ 65 years were enrolled, 53% between 71 and 79 years old. Cumulative Illness Rating Scale (CIRS) comorbidity score was ≥6 in 54% patients. Overall survival (OS) at 12 months was 95% (95% confidence interval [CI]: 90–97%); after a median follow up of 50 months, median OS was 84 months. The overall response rate was 87%, with 56% complete responses; the median time to progression (TTP) was 61 months. The baseline factors affecting OS by multivariable analysis were sex, histological diagnosis, renal function, and planned bendamustine dose, while only type of lymphoma and bendamustine dose impacted on TTP. Main adverse events were neutropenia (grade ≥ 3: 43%) and infections (any grade: 36%), with 17% of patients requiring hospital admission. Conclusions: The responses to bendamustine, as well as survival, are relevant even in advanced age patients, with a manageable incidence of acute toxicity. |
format | Online Article Text |
id | pubmed-8066290 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-80662902021-04-25 Real Life Use of Bendamustine in Elderly Patients with Lymphoid Neoplasia Dogliotti, Irene Ragaini, Simone Vassallo, Francesco Boccellato, Elia De Luca, Gabriele Perutelli, Francesca Boccomini, Carola Clerico, Michele Botto, Barbara Grimaldi, Daniele Orsucci, Lorella Ferrero, Simone Vitale, Candida Ferrero, Dario Coscia, Marta Cavallo, Federica J Pers Med Article Background. Bendamustine is a cytotoxic alkylating drug with a broad range of indications as a single agent or in combination therapy in lymphoid neoplasia patients. However, its tolerability in elderly patients is still debated. Methods: An observational, retrospective study was carried out; patients with chronic lymphocytic leukemia (CLL) or lymphoma, aged ≥ 65 years old, treated with bendamustine-based regimens in first or subsequent lines between 2010 and 2020 were considered eligible. Results: Overall, 179 patients aged ≥ 65 years were enrolled, 53% between 71 and 79 years old. Cumulative Illness Rating Scale (CIRS) comorbidity score was ≥6 in 54% patients. Overall survival (OS) at 12 months was 95% (95% confidence interval [CI]: 90–97%); after a median follow up of 50 months, median OS was 84 months. The overall response rate was 87%, with 56% complete responses; the median time to progression (TTP) was 61 months. The baseline factors affecting OS by multivariable analysis were sex, histological diagnosis, renal function, and planned bendamustine dose, while only type of lymphoma and bendamustine dose impacted on TTP. Main adverse events were neutropenia (grade ≥ 3: 43%) and infections (any grade: 36%), with 17% of patients requiring hospital admission. Conclusions: The responses to bendamustine, as well as survival, are relevant even in advanced age patients, with a manageable incidence of acute toxicity. MDPI 2021-03-30 /pmc/articles/PMC8066290/ /pubmed/33808164 http://dx.doi.org/10.3390/jpm11040249 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 Dogliotti, Irene Ragaini, Simone Vassallo, Francesco Boccellato, Elia De Luca, Gabriele Perutelli, Francesca Boccomini, Carola Clerico, Michele Botto, Barbara Grimaldi, Daniele Orsucci, Lorella Ferrero, Simone Vitale, Candida Ferrero, Dario Coscia, Marta Cavallo, Federica Real Life Use of Bendamustine in Elderly Patients with Lymphoid Neoplasia |
title | Real Life Use of Bendamustine in Elderly Patients with Lymphoid Neoplasia |
title_full | Real Life Use of Bendamustine in Elderly Patients with Lymphoid Neoplasia |
title_fullStr | Real Life Use of Bendamustine in Elderly Patients with Lymphoid Neoplasia |
title_full_unstemmed | Real Life Use of Bendamustine in Elderly Patients with Lymphoid Neoplasia |
title_short | Real Life Use of Bendamustine in Elderly Patients with Lymphoid Neoplasia |
title_sort | real life use of bendamustine in elderly patients with lymphoid neoplasia |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8066290/ https://www.ncbi.nlm.nih.gov/pubmed/33808164 http://dx.doi.org/10.3390/jpm11040249 |
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