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Comparable safety profile of BeEAM (bendamustine, etoposide, cytarabine, melphalan) and BEAM (carmustine, etoposide, cytarabine, melphalan) as conditioning before autologous haematopoietic cell transplantation

INTRODUCTION: BEAM (carmustine, etoposide, cytarabine, melphalan) is the most frequently used high-dose chemotherapy regimen for patients with lymphoma referred for autologous haematopoietic cell transplantation (autoHCT). Recently, a novel conditioning protocol containing bendamustine instead of ca...

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Autores principales: Frankiewicz, Andrzej, Saduś-Wojciechowska, Maria, Najda, Jacek, Czerw, Tomasz, Mendrek, Włodzimierz, Sobczyk-Kruszelnicka, Małgorzata, Soska, Katarzyna, Ociepa, Małgorzata, Hołowiecki, Jerzy, Giebel, Sebastian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103227/
https://www.ncbi.nlm.nih.gov/pubmed/30150889
http://dx.doi.org/10.5114/wo.2018.77046
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author Frankiewicz, Andrzej
Saduś-Wojciechowska, Maria
Najda, Jacek
Czerw, Tomasz
Mendrek, Włodzimierz
Sobczyk-Kruszelnicka, Małgorzata
Soska, Katarzyna
Ociepa, Małgorzata
Hołowiecki, Jerzy
Giebel, Sebastian
author_facet Frankiewicz, Andrzej
Saduś-Wojciechowska, Maria
Najda, Jacek
Czerw, Tomasz
Mendrek, Włodzimierz
Sobczyk-Kruszelnicka, Małgorzata
Soska, Katarzyna
Ociepa, Małgorzata
Hołowiecki, Jerzy
Giebel, Sebastian
author_sort Frankiewicz, Andrzej
collection PubMed
description INTRODUCTION: BEAM (carmustine, etoposide, cytarabine, melphalan) is the most frequently used high-dose chemotherapy regimen for patients with lymphoma referred for autologous haematopoietic cell transplantation (autoHCT). Recently, a novel conditioning protocol containing bendamustine instead of carmustine (BeEAM) has been proposed to potentially increase the efficacy. AIM OF THE STUDY: The aim of this study was to retrospectively compare the safety profile of BEAM and BeEAM based on single-centre experience. MATERIAL AND METHODS: A total of 237 consecutive patients with lymphoma treated with either BEAM (n = 174) or BeEAM (n = 63), between the years 2011 and 2016, were included in the analysis. Clinical characteristics of both groups were comparable. Patients with Hodgkin’s lymphoma (HL) constituted 49% of the BEAM group and 40% of the BeEAM group. RESULTS: Median time to neutrophil > 0.5 × 10(9)/l recovery was 10 days in both groups (p = 0.29), while median time to platelet > 50 × 10(9)/l recovery was 13 and 14 days after BEAM and BeEAM, respectively (p = 0.12). The toxicity profile was comparable except for arterial hypertension and severe hypokalaemia, which occurred more frequently after BeEAM compared to BEAM (p = 0.02 and p = 0.004, respectively). The rate of early mortality was 1.7% and 1.6%, respectively. The probabilities of the overall and progression-free survival were comparable for both groups (p = 0.73 and p = 0.55, respectively). CONCLUSIONS: Administration of bendamustine instead of carmustine as part of conditioning does not affect the engraftment or the toxicity profile of the regimen. Therefore, BeEAM may be safely used in patients with lymphoma undergoing autoHCT. Its efficacy requires evaluation in prospective studies.
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spelling pubmed-61032272018-08-27 Comparable safety profile of BeEAM (bendamustine, etoposide, cytarabine, melphalan) and BEAM (carmustine, etoposide, cytarabine, melphalan) as conditioning before autologous haematopoietic cell transplantation Frankiewicz, Andrzej Saduś-Wojciechowska, Maria Najda, Jacek Czerw, Tomasz Mendrek, Włodzimierz Sobczyk-Kruszelnicka, Małgorzata Soska, Katarzyna Ociepa, Małgorzata Hołowiecki, Jerzy Giebel, Sebastian Contemp Oncol (Pozn) Original Paper INTRODUCTION: BEAM (carmustine, etoposide, cytarabine, melphalan) is the most frequently used high-dose chemotherapy regimen for patients with lymphoma referred for autologous haematopoietic cell transplantation (autoHCT). Recently, a novel conditioning protocol containing bendamustine instead of carmustine (BeEAM) has been proposed to potentially increase the efficacy. AIM OF THE STUDY: The aim of this study was to retrospectively compare the safety profile of BEAM and BeEAM based on single-centre experience. MATERIAL AND METHODS: A total of 237 consecutive patients with lymphoma treated with either BEAM (n = 174) or BeEAM (n = 63), between the years 2011 and 2016, were included in the analysis. Clinical characteristics of both groups were comparable. Patients with Hodgkin’s lymphoma (HL) constituted 49% of the BEAM group and 40% of the BeEAM group. RESULTS: Median time to neutrophil > 0.5 × 10(9)/l recovery was 10 days in both groups (p = 0.29), while median time to platelet > 50 × 10(9)/l recovery was 13 and 14 days after BEAM and BeEAM, respectively (p = 0.12). The toxicity profile was comparable except for arterial hypertension and severe hypokalaemia, which occurred more frequently after BeEAM compared to BEAM (p = 0.02 and p = 0.004, respectively). The rate of early mortality was 1.7% and 1.6%, respectively. The probabilities of the overall and progression-free survival were comparable for both groups (p = 0.73 and p = 0.55, respectively). CONCLUSIONS: Administration of bendamustine instead of carmustine as part of conditioning does not affect the engraftment or the toxicity profile of the regimen. Therefore, BeEAM may be safely used in patients with lymphoma undergoing autoHCT. Its efficacy requires evaluation in prospective studies. Termedia Publishing House 2018-06-30 2018 /pmc/articles/PMC6103227/ /pubmed/30150889 http://dx.doi.org/10.5114/wo.2018.77046 Text en Copyright: © 2018 Termedia Sp. z o. o. http://creativecommons.org/licenses/by-nc-sa/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) License, allowing third parties to copy and redistribute the material in any medium or format and to remix, transform, and build upon the material, provided the original work is properly cited and states its license.
spellingShingle Original Paper
Frankiewicz, Andrzej
Saduś-Wojciechowska, Maria
Najda, Jacek
Czerw, Tomasz
Mendrek, Włodzimierz
Sobczyk-Kruszelnicka, Małgorzata
Soska, Katarzyna
Ociepa, Małgorzata
Hołowiecki, Jerzy
Giebel, Sebastian
Comparable safety profile of BeEAM (bendamustine, etoposide, cytarabine, melphalan) and BEAM (carmustine, etoposide, cytarabine, melphalan) as conditioning before autologous haematopoietic cell transplantation
title Comparable safety profile of BeEAM (bendamustine, etoposide, cytarabine, melphalan) and BEAM (carmustine, etoposide, cytarabine, melphalan) as conditioning before autologous haematopoietic cell transplantation
title_full Comparable safety profile of BeEAM (bendamustine, etoposide, cytarabine, melphalan) and BEAM (carmustine, etoposide, cytarabine, melphalan) as conditioning before autologous haematopoietic cell transplantation
title_fullStr Comparable safety profile of BeEAM (bendamustine, etoposide, cytarabine, melphalan) and BEAM (carmustine, etoposide, cytarabine, melphalan) as conditioning before autologous haematopoietic cell transplantation
title_full_unstemmed Comparable safety profile of BeEAM (bendamustine, etoposide, cytarabine, melphalan) and BEAM (carmustine, etoposide, cytarabine, melphalan) as conditioning before autologous haematopoietic cell transplantation
title_short Comparable safety profile of BeEAM (bendamustine, etoposide, cytarabine, melphalan) and BEAM (carmustine, etoposide, cytarabine, melphalan) as conditioning before autologous haematopoietic cell transplantation
title_sort comparable safety profile of beeam (bendamustine, etoposide, cytarabine, melphalan) and beam (carmustine, etoposide, cytarabine, melphalan) as conditioning before autologous haematopoietic cell transplantation
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6103227/
https://www.ncbi.nlm.nih.gov/pubmed/30150889
http://dx.doi.org/10.5114/wo.2018.77046
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