Evidence map›Paper›PMID 35439293›Full record

Trial reportBlood advances2022

Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma.

Diego Villa, Eva Hoster, Olivier Hermine, Wolfram Klapper, Michal Szymczyk, André Bosly, Michael Unterhalt, Lisa M Rimsza, Colleen A Ramsower, Ciara L Freeman and 5 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Blood advances, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
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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 6 countries.

Diego VillaBC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-4625-3009
Eva HosterInstitute for Medical Information Processing, Biometry, and Epidemiology, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID 0000-0002-0749-1389
Olivier HermineHôpital Necker, Assistance Publique Hôpitaux de Paris, University of Paris Descartes, Paris, France.
Wolfram KlapperDepartment of Pathology, Hematopathology Section, University-Hospital Schleswig-Holstein, University of Kiel, Kiel, Germany.ORCID 0000-0001-7208-4117
Michal SzymczykDepartment of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
André BoslyCentre Hospitalier Universitaire - Université Catholique de Louvain Mont-Godinne-Dinant, Yvoir, Belgium.
Michael UnterhaltMedizinische Klinik III, Ludwig-Maximilians-Universität München, Munich, Germany.
Lisa M RimszaDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Scottsdale, AZ; and.
Colleen A RamsowerDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Scottsdale, AZ; and.
Ciara L FreemanH. Lee Moffitt Cancer Centre & Research Institute and Morsani College of Medicine, University of South Florida, Tampa, FL.
David W ScottBC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-0435-5947
Alina S GerrieBC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0003-4727-1425
Kerry J SavageBC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.ORCID 0000-0002-5835-9863
Laurie H SehnBC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.
Martin DreylingMedizinische Klinik III, Ludwig-Maximilians-Universität München, Munich, Germany.ORCID 0000-0002-0358-5249
University of British Columbia · CALudwig-Maximilians-Universität München · DEMayo Clinic in Arizona · USHôpital Necker-Enfants Malades · FRThe Maria Sklodowska-Curie National Research Institute of Oncology · PLUCLouvain · BEUniversity Hospital Schleswig-Holstein · DEUniversity of South Florida · US

Funding

Development of Mantle Cell Lymphoma Proliferation Signature AssayUH3CA217847 · NCI · MAYO CLINIC ARIZONA · PI RIMSZA, LISA · 2019 to 2021
$1.0M
Development of Mantle Cell Lymphoma Proliferation Signature AssayUH2CA217847 · NCI · MAYO CLINIC ARIZONA · PI RIMSZA, LISA · 2017 to 2018
$397k
NCI NIH HHS UH2 CA217847NCI NIH HHS UH3 CA217847
6 · The paper itself

Abstract

The objective of this study was to explore differences in outcomes between first-line rituximab plus bendamustine (R-B) and R-CHOP/R-DHAP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone, dexamethasone, cytarabine, cisplatin) in transplant-eligible patients with mantle cell lymphoma (MCL). A population-based cohort of 97 patients aged 18 to 65 years with stage II-IV MCL, consecutively treated with R-B was retrospectively identified at BC Cancer. Baseline characteristics, response rates, and outcomes were compared with the cohort of 232 patients with MCL randomized to the R-CHOP/R-DHAP arm of the MCL Younger trial. The primary endpoint was the hazard ratio (HR) of the progression-free survival (PFS) comparison between both groups, adjusted for MCL International Prognostic Index (MIPI), Ki67 index, and blastoid/ pleomorphic morphology. Ann Arbor stage, lactate dehydrogenase, MIPI, blastoid morphology, and MCL35 assignments were similar between both groups. The overall response rate (ORR) to R-B was 90% (54% complete response [CR]); 77% of patients proceeded to autologous stem cell transplantation (ASCT) and 78% received maintenance rituximab (MR). The ORR to R-CHOP/R-DHAP was 94% (54% CR); 78% proceeded to ASCT and 2% received MR. There were no differences in PFS in unadjusted (HR, 0.87; 95% confidence interval [CI], 0.53-1.41; P = .56) or adjusted (HR, 0.79; 95% CI, 0.45-1.37; P = .40) comparisons. There were no clear differences in secondary endpoints in unadjusted or adjusted analyses. This retrospective adjusted comparison of 2 independent cohorts of younger patients with MCL suggests that R-B with ASCT and maintenance rituximab is a feasible and effective first-line treatment, with outcomes comparable to R-CHOP/R-DHAP with ASCT.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoma, Mantle-CellAdolescentAdultAgedAntineoplastic Combined Chemotherapy ProtocolsBendamustine HydrochlorideCisplatinCyclophosphamideCytarabineDexamethasoneDoxorubicinHumansKi-67 AntigenLactate DehydrogenasesMiddle AgedBendamustine HydrochlorideCisplatinCyclophosphamideCytarabineDexamethasoneDoxorubicinKi-67 AntigenLactate DehydrogenasesPrednisoneRituximabVincristine

Identifiers

PMID35439293
PMCPMC9631687
OpenAlexW4224247201

What OpenQuestion holds

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LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.