Evidence map›Paper›PMID 40422544›Full record

ArticleCurrent oncology (Toronto, Ont.)2025

Allogeneic Hematopoietic Cell Transplant for B-Cell Lymphomas in the Era of Novel Cellular Therapies: Experience from a Tertiary Canadian Center.

Mathias Castonguay, Jean Roy, Jean-Sébastien Claveau, Sylvie Lachance, Jean-Sébastien Delisle, Thomas Kiss, Sandra Cohen, Isabelle Fleury, Luigina Mollica, Imran Ahmad and 5 more

Abstract read
In one paragraph

Article in Current oncology (Toronto, Ont.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Review
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.

Mathias CastonguayHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.ORCID 0000-0002-9281-8015
Jean RoyHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.ORCID 0000-0002-7716-6864
Jean-Sébastien ClaveauHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.ORCID 0000-0003-2638-5773
Sylvie LachanceHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.ORCID 0000-0001-7882-9335
Jean-Sébastien DelisleHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.ORCID 0000-0003-1460-7287
Thomas KissHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.
Sandra CohenHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.
Isabelle FleuryHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.
Luigina MollicaHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.
Imran AhmadHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.ORCID 0000-0003-1899-0164
Nadia BambaceHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.
Léa BernardHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.
Denis-Claude RoyHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.ORCID 0000-0002-5921-1692
Guy SauvageauHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.
Olivier VeilleuxHematology-Oncology and Cell Therapy University Institute, Hôpital Maisonneuve-Rosemont Research Center, Université de Montréal, Montréal, QC H1T 2M4, Canada.ORCID 0000-0002-7029-1769

Funding

Famille Casser Fund Philanthropic fund, no grand number
6 · The paper itself

Abstract

backgroundAllogeneic hematopoietic cell transplant (alloHCT) is a curative option for relapsed/refractory B-cell lymphomas (BCLs), but its role in the evolving field of cellular therapy is increasingly unclear as recent advances in transplant procedures have improved outcomes.

methodsThis retrospective, single-center study included 55 BCL patients (large B-cell lymphoma-LBCL; indolent BCL; and mantle cell lymphoma-MCL) treated with alloHCT from 2015 to 2023 at Hôpital Maisonneuve-Rosemont. Primary endpoints were overall survival (OS) and progression-free survival (PFS); secondary endpoints included NRM and GVHD incidence.

resultsA total of 55 patients were included (25 LBCLs, 16 indolent BCLs, 14 MCLs), and 76% of LBCLs were of indolent origin (Richter transformation, transformed follicular lymphoma). After a median follow-up of 6.1, 5.8 and 2.4 years for LBCLs, indolent BCLs and MCLs, their 5-year PFS and OS were 57.2% (IC 95%: 34.2-74.7) and 62.8% (IC 95%: 37.9-80.0), 81.2% (IC 95%: 52.5-93.5) and 93.8% (IC 95%: 63.2-99.1), and 39.0% (IC 95%: 14.3-63.3) and 68.1% (IC 95%: 35.4-86.8), respectively. The 5-year NRM was 16.9% (IC 95%: 8.2-28.3) with a relapse incidence of 23.4%. Overall/grade 3-4 acute GVHD occurred in 43.6% and 18.1% of patients. At 3 years, overall/moderate or severe chronic GVHD incidence was 49% and 34.5%.

conclusionsAlloHCT remains a potentially curative option and should be considered for fit patients with chemosensitive FL or LBCLs of indolent origin and a low comorbidity index.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoma, B-CellAdultAgedCanadaFemaleGraft vs Host DiseaseHumansMaleMiddle AgedRetrospective StudiesTertiary Care CentersTransplantation, Homologousallogeneic hematopoietic cell transplantB-cell lymphomacell therapy

Identifiers

PMID40422544
PMCPMC12109923

What OpenQuestion holds

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LicenceCC BY
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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.