Evidence map›Paper›PMID 39213423›Full record

ArticleBlood advances2024

Autologous stem cell transplantation in T-cell/histiocyte-rich large B-cell lymphoma: EBMT Lymphoma Working Party study.

Simon Renders, Maud Ngoya, Herve Finel, Marie-Thérèse Rubio, William Townsend, Roland Schroers, Urban Novak, Nicolaas Schaap, Mahmoud Aljurf, Grzegorz Helbig and 10 more

Abstract read
In one paragraph

Article in Blood advances, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Article
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

20 authors.

Simon RendersDepartment of Internal Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0001-7883-2956
Maud NgoyaLymphoma Working Party, European Society for Blood and Marrow Transplantation Central Registry Office, Paris, France.ORCID 0000-0002-7810-6900
Herve FinelLymphoma Working Party, European Society for Blood and Marrow Transplantation Central Registry Office, Paris, France.ORCID 0000-0002-0432-9765
Marie-Thérèse RubioHematology Unite, Centre Hospitalier Régional Universitaire de Nancy, Vandoeuvre Nancy, France.
William TownsendDepartment of Hematology, University College London Hospitals, London, United Kingdom.ORCID 0000-0003-3975-2448
Roland SchroersDepartment of Hematology, Oncology, Stem Cell Transplantation and Cell Therapy, Ruhr-University Bochum, Knappschaftskrankenhaus, Bochum, Germany.ORCID 0000-0003-2744-5491
Urban NovakDepartment of Medical Oncology, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Nicolaas SchaapDepartment of Hematology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Mahmoud AljurfOncology Center, King Faisal Specialist Hospital & Research Centre, Riyadh, Saudi Arabia.
Grzegorz HelbigDepartment of Hematology, Medical University of Silesia, Katowice, Poland.ORCID 0000-0003-3703-1268
Matthew CollinDepartment of Hematology, Freeman Hospital, Newcastle upon Tyne, United Kingdom.ORCID 0000-0001-6585-9586
Guido KobbeDepartment of Hematology Oncology and Clinical Immunology, Heinrich-Heine-Universitaet, Duesseldorf, Germany.
Anne HuynhDepartment of Hematology, Institut Universitaire du Cancer, Toulouse, France.
José Antonio Pérez-SimónDepartment of Hematology, Hospital Universitario Virgen del Rocío, Instituto de Biomedicina de Sevilla, Universidad de Sevilla, Sevilla, Spain.
Adrian BloorDepartment of Hematology, The Christie NHS Foundation Trust, Manchester, United Kingdom.
Hervé GhesquieresDepartment of Hematology, Hospices Civils de Lyon, Lyon, France.
Anna SuredaDepartment of clinical hematology, Catalan Institute of Oncology-Hospitalet, Barcelona, Spain.ORCID 0000-0002-1238-6970
Norbert SchmitzDepartment of Medicine A, University Hospital Muenster, Muenster, Germany.
Bertram GlassKlinik für Hümatologie und Stammzelltransplantation, Helios Klinikum Berlin-Buch, Berlin, Germany.
Peter DregerDepartment of Internal Medicine V, Hematology, Oncology and Rheumatology, Heidelberg University Hospital, Heidelberg, Germany.ORCID 0000-0002-7429-8570

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractAlthough broadly used, consolidative autologous hematopoietic stem cell transplantation (auto-HCT) for relapsed/refractory (R/R) T-cell/histiocyte-rich large B-cell lymphoma (THRLBCL) has never been specifically investigated. Here, we have analyzed outcomes of auto-HCT for THRLBCL compared with diffuse large cell B-cell lymphoma not otherwise specified (DLBCL). Eligible for this retrospective registry study were adult patients with R/R THRLBCL and DLBCL, respectively, who underwent a first auto-HCT in a salvage-sensitive disease status as assessed by positron emission tomography-computed tomography between 2016 and 2021 and were registered with the European Society for Blood and Marrow Transplantation database. The primary end point was progression-free survival (PFS) 2 years after transplantation. A total of 201 patients with THRLBCL and 5543 with DLBCL were included. There were no significant differences in terms of disease status at HCT, pretreatment lines, and interval from diagnosis to transplant between the cohorts, but patients with THRLBCL were significantly younger, contained a higher proportion of men, and had a better performance status. Compared with DLBCL, THRLBCL was associated with significantly better 2-year PFS (78% vs 59%; P < .001) and overall survival (OS, 81% vs 74%; P = .02) because of a significantly lower 2-year relapse incidence (16% vs 35%; P < .001). On multivariate analysis, favorable relapse risk (hazard ratio [HR], 0.46; 95% confidence interval [CI], 0.31-0.7) and PFS (HR, 0.58; 95% CI, 0.41-0.82) of patients with THRLBCL remained significant, whereas OS benefits (HR, 0.78; 95% CI, 0.54-1.12) did not. These results were validated in a propensity score-matched analysis. These data prove auto-HCT as an effective treatment option for salvage-sensitive R/R THRLBCL.

Indexed as

Hematopoietic Stem Cell TransplantationLymphoma, Large B-Cell, DiffuseTransplantation, AutologousAdultAgedFemaleHumansMaleMiddle AgedRetrospective StudiesT-LymphocytesTreatment OutcomeYoung Adult

Identifiers

PMID39213423
PMCPMC11541691

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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.