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A comparison of GIT toxicity of the BEAM and TEAM conditioning before autologous transplantation in patients with lymphomas


Authors: B. Břízová;  A. Jungová;  D. Lysák;  J. Šrámek;  V. Bergerová;  P. Jindra
Authors‘ workplace: Hematologicko-onkologické oddělení, FN Plzeň
Published in: Transfuze Hematol. dnes,29, 2023, No. 4, p. 259-262.
Category: Original Papers
doi: https://doi.org/10.48095/cctahd2023prolekare.cz13

Overview

The BEAM regimen, i.e., carmustine (BCNU) in combination with etoposide, cytarabine, and melphalan was used as standard conditioning prior to autologous hematopoietic cell transplantation (ASCT) in relapsed or refractory lymphomas. However, the recent unavailability of BCNU necessitated the use of an alternative regimen, which in our centre became from July 2018 the so-called TEAM regimen containing thiotepa. We decided to retrospectively compare the gastrointestinal (GIT) toxicity of both conditioning regimens. We included 142 consecutive autologous transplant patients (BEAM = 82, TEAM = 60), of whom 31% had diffuse large B-cell lymphoma (DLBCL), 20% Hodgkin‘s lymphoma (HL), 15 % mantle cell lymphoma (MCL), 14% T-cell lymphomas (T-NHL) and the remaining 20% other types of non-Hodgkin lymphomas (NHL). Both cohorts were comparable in terms of patient age, prevalence of diagnoses, and disease status at the time of ASCT. There was no statistically significant difference in the distribution of the grades of GIT toxicity between the two cohorts, even after grouping all grades into two main groups of patients (grade 0+1 vs. grade 2–4). Patients receiving the TEAM regimen were more likely to require parenteral nutrition, namely in 20 cases (33%) versus only 13 cases (16%) in the BEAM regimen (P = 0.04). Non-relapse mortality (NRM) was comparably low for both regimens – 0% during hospitalization and 2% at 3 months for both conditioning regimens (P = 1.0). We also compared overall survival (OS) and progression-free survival (PFS): there was no statistically significant difference between the two cohorts (P = 0.59 for OS, P = 0.1 for PFS).

Keywords:

conditioning – autologous haematopoietic cell transplantation – lymphoma – GIT toxicity – carmustine – thiotepa


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Haematology Internal medicine Clinical oncology
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