Evidence map›Paper›PMID 38024477›Full record

ArticleEClinicalMedicine2023

BendaEAM versus BEAM as conditioning regimen for ASCT in patients with relapsed lymphoma (BEB): a multicentre, randomised, phase 2 trial.

Felix Keil, Antonia M S Müller, Andrea Berghold, Regina Riedl, Veronika Buxhofer-Ausch, Judith Schuster, Corinne Vorburger, Alexandra Böhm, Michael Panny, Thomas Nösslinger and 5 more

Open access · goldAbstract read
In one paragraph

Article in EClinicalMedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.0field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed, 4 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

15 authors at 8 institutions in 2 countries.

Felix Keil3rd Medical Department for Haematology and Oncology, Hanusch Hospital, Vienna, Austria.
Antonia M S MüllerDepartment of Transfusion Medicine and Cell Therapy, Medical University of Vienna, Vienna, Austria.
Andrea BergholdInstitute for Medical Informatics, Statistics, and Documentation, Medical University Graz, Graz, Austria.
Regina RiedlInstitute for Medical Informatics, Statistics, and Documentation, Medical University Graz, Graz, Austria.
Veronika Buxhofer-AuschDepartment of Internal Medicine I with Haematology, Stem Cell Transplantation, Haemostaseology and Medical Oncology, Ordensklinikum Linz Elisabethinen, Linz, Austria.
Judith SchusterAustrian Group Medical Tumor Therapy (AGMT), Salzburg, Austria.
Corinne VorburgerDepartment of Medical Oncology, Inselspital, Bern University Hospital, Bern, Switzerland.
Alexandra BöhmHaematological Health Care Centre of the ÖGK Mariahilf, Vienna, Austria.
Michael Panny3rd Medical Department for Haematology and Oncology, Hanusch Hospital, Vienna, Austria.
Thomas Nösslinger3rd Medical Department for Haematology and Oncology, Hanusch Hospital, Vienna, Austria.
Richard GreilAustrian Group Medical Tumor Therapy (AGMT), Salzburg, Austria.
Panagiotis SamarasClinic for Haematology and Oncology Hirslanden Zurich, Zurich, Switzerland.
Celine Bencker3rd Medical Department for Haematology and Oncology, Hanusch Hospital, Vienna, Austria.
Markus RüttiDepartment of Medical Oncology and Haematology, University Hospital Zurich, Zurich, Switzerland.
Thomas PabstDepartment of Medical Oncology, Inselspital, Bern University Hospital, Bern, Switzerland.
Hanusch Hospital · ATMedical University of Graz · ATUniversity Hospital of Bern · CHUniversity Hospital of Zurich · CHAustrian Breast & Colorectal Cancer Study Group · ATJohannes Kepler University of Linz · ATKlinik Hirslanden · CHUniversity of Salzburg · AT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Replacement of carmustine (BCNU) in the BEAM regimen (BCNU, etoposide, cytarabine, melphalan) with bendamustine (BendaEAM) before autologous stem cell transplantation (ASCT) is feasible in lymphoma. However, randomised trials are lacking. Here, we present the first trial addressing this topic. Methods: This multicentre, randomised, phase 2 study (BEB-trial) conducted at four haematological centres in Austria and Switzerland compares BEAM with BendaEAM in patients with relapsed lymphoma. Both regimens were administered intravenously before ASCT, in BEAM according to the standard protocol (300 mg/m Findings: Between April 20, 2015, and November 28, 2018, 108 patients were enrolled; of whom 53 were randomly assigned to receive BendaEAM (36 male, 17 female) and 55 to receive BEAM (39 male, 16 female). All patients engrafted rapidly. Lung toxicity did not differ between groups (BendaEAM: n = 8, 19.5%; BEAM: n = 11, 25.6%; risk difference = -6.1%: 95% confidence interval: -23.9% to 11.7%). Acute toxicities of at least grade 3 were comparable in both groups (BendaEAM: 35.8%, BEAM: 30.9%). Overall survival (BendaEAM: 92.5%, BEAM: 89.1%) and complete remission (BendaEAM: 76.7%, BEAM: 74.3%) after 1 year (median follow-up: 369 days) were similar. No difference in quality of life was observed. Interpretation: Results were similar for both regimens in terms of survival and response rates. A phase 3 non-inferiority study is required to investigate whether BendaEAM can be considered as an alternative to BEAM. Funding: Mundipharma.

Indexed as

Autologous stem cell transplantationBEAMBendamustineConditioning regimenLymphoma

Identifiers

PMID38024477
PMCPMC10679477
OpenAlexW4388808520

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.