Evidence map›Paper›PMID 31953532›Full record

ArticleBone marrow transplantation2020

Bendamustine-EAM versus BEAM regimen in patients with mantle cell lymphoma undergoing autologous stem cell transplantation in the frontline setting: a multicenter retrospective study from Lymphoma Study Association (LYSA) centers.

Thomas Hueso, Thomas Gastinne, Sylvain Garciaz, Emmanuelle Tchernonog, Caroline Delette, René-Olivier Casasnovas, Eric Durot, Roch Houot, Benoît Tessoulin, Olivier Tournilhac and 16 more

Abstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Bone marrow transplantation, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% 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

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 citations in OpenAlex.

  1. Pooled it
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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

26 authors at 16 institutions in 2 countries.

Thomas HuesoDepartment of Clinical Hematology, Caen University Hospital, F-14000, Caen, France.ORCID http://orcid.org/0000-0003-3354-332X
Thomas GastinneDepartment of Clinical Hematology, Nantes University Hospital, Nantes, France.
Sylvain GarciazDepartment of Clinical Hematology, Paoli Calmettes Institute, Marseille, France.
Emmanuelle TchernonogDepartment of Clinical Hematology, Montpellier University Hospital, Montpellier, France.
Caroline DeletteDepartment of Clinical Hematology, Amiens University Hospital, Amiens, France.
René-Olivier CasasnovasDepartment of Clinical Hematology, François Mitterrand University Hospital, Dijon, France.
Eric DurotDepartment of Clinical Hematology, Reims University Hospital, Reims, France.
Roch HouotDepartment of Clinical Hematology, Rennes University Hospital, F-35033, Rennes, France.
Benoît TessoulinDepartment of Clinical Hematology, Nantes University Hospital, Nantes, France.
Olivier TournilhacDepartment of Clinical Hematology, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.
Sandra MalakDepartment of Clinical Hematology, Curie Institute, René Huguenin Hospital, Saint-Cloud, France.
Emmanuel GyanDepartment of Clinical Hematology, Tours University Hospital, Tours, France.
Luc-Matthieu ForneckerDepartment of Clinical Hematology, Strasbourg University Hospital, Strasbourg, France.
Julie AbrahamDepartment of Clinical Hematology, Limoges University Hospital, Limoges, France.
Baptiste DelapierreDepartment of Clinical Hematology, Caen University Hospital, F-14000, Caen, France.
Frédéric PeyradeDepartment of Clinical Hematology, Antoine Lacassagne Center, Nice, France.
Richard LemalDepartment of Clinical Hematology, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.
Rémy GressinDepartment of Clinical Hematology, Grenoble University Hospital, Grenoble, France.
Sylvain ChantepieDepartment of Clinical Hematology, Caen University Hospital, F-14000, Caen, France.
Cécile BorelDepartment of Clinical Hematology, Toulouse Oncopole, Toulouse, France.
Rémy MorelloDepartment of Biostatistics and Clinical Research, Caen University Hospital, F-14000, Caen, France.
Krimo BouabdallahDepartment of Clinical Hematology, Bordeaux University Hospital, France, France.
Ahmad IbrahimDepartment of Clinical Hematology, Makassed General Hospital, Beirut, Libanon, France.
Reda BouabdallahDepartment of Clinical Hematology, Paoli Calmettes Institute, Marseille, France.
Steven Le GouillDepartment of Clinical Hematology, Nantes University Hospital, Nantes, France.
Gandhi DamajDepartment of Clinical Hematology, Caen University Hospital, F-14000, Caen, France. Gandhi.damaj@unicaen.fr.
Inserm · FRCentre Hospitalier Universitaire de Caen Normandie · FRInstitut Pprime · FRCentre Antoine Lacassagne · FRCentre Hospitalier Universitaire Amiens-Picardie · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Reims · FRHôpital René Huguenin · FRHôpital Universitaire Dupuytren · FRHôpitaux Universitaires de Strasbourg · FRInstitut universitaire du cancer de Toulouse Oncopole · FRMakassed General Hospital · LBNormandie Université · FRUniversité de Bordeaux · FRUniversité de Montpellier · FRUniversité de Tours · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The combination of carmustine, etoposide, cytarabine, and melphalan (BEAM) as conditioning regimen prior to autologous stem-cell transplantation (ASCT) remains the standard of care for patients with mantle cell lymphoma (MCL) who are eligible for transplantation. The replacement of carmustine with bendamustine (BeEAM) was described as a promising alternative in non-Hodgkin lymphoma. The aim of this retrospective study was to compare the BeEAM with the BEAM regimen in MCL patients in the frontline setting. Sixty and 108 patients were included in the BeEAM and the BEAM groups, respectively. At 3 years, progression-free survival (PFS) was significantly higher in the BeEAM than in the BEAM group (84% [73-96] vs. 63% [51-79], p = 0.03). The overall survival was not statistically different between the two groups (p = 0.2). In multivariable analysis, BeEAM regimen remained associated with higher PFS (HR = 0.377, 95% CI, 0.146-0.970; p = 0.043). Subgroup analyses in patients treated with prior rituximab-aracytine induction alone showed that BeEAM improved the PFS compared with BEAM regimen (p = 0.04). Despite the high rate of acute renal failure KDIGO III (32%), treatment-related mortality was not increased with the BeEAM regimen. A prospective randomized trial will be necessary to confirm the beneficial effect of the BeEAM regimen in MCL patients undergoing ASCT.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoma, Mantle-CellAdultAntineoplastic Combined Chemotherapy ProtocolsBendamustine HydrochlorideCarmustineCytarabineEtoposideHumansMelphalanProspective StudiesRetrospective StudiesTransplantation, AutologousBendamustine HydrochlorideCarmustineCytarabineEtoposideMelphalan

Identifiers

PMID31953532
OpenAlexW3000354870

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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.