Evidence map›Paper›PMID 38181767›Full record

ArticleBlood advances2024

Transfusion needs after CAR T-cell therapy for large B-cell lymphoma: predictive factors and outcome (a DESCAR-T study).

Samuel Vic, Jean-Baptiste Thibert, Emmanuel Bachy, Guillaume Cartron, Thomas Gastinne, Franck Morschhauser, Fabien Le Bras, Kamal Bouabdallah, Fabien Despas, Jacques-Olivier Bay and 12 more

Open access · goldAbstract 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 20 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed, 1 pooled it
6.5field-weighted citation impact, top 2% 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

20 citing papers in PubMed, 1 synthesis or guideline pooled it, 23 citations in OpenAlex.

  1. Pooled it
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  8. Platelet Transfusion for Patients with Cancer: An Update.Transfusion medicine and hemotherapy : offizielles Organ der Deutschen Gesellschaft fur Transfusionsmedizin und Immunhamatologie · 2025
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 19 institutions in 1 country.

Samuel VicDepartment of Hematology, CHU de Rennes, Rennes, France.ORCID 0000-0002-1038-0452
Jean-Baptiste ThibertEtablissement français du sang Bretagne, Rennes, France.ORCID 0000-0002-8721-8357
Emmanuel BachyHematology Department, CHU Lyon Sud, Pierre Bénite, Lyon, France.ORCID 0000-0003-2694-7510
Guillaume CartronHematology Department, CHU de Montpellier, Montpellier, France.ORCID 0000-0003-0659-9635
Thomas GastinneHematology Department CHU de Nantes, Nantes, France.
Franck MorschhauserDepartment of Hematology CHU de Lille, Université de Lille, Lille, France.ORCID 0000-0002-3714-9824
Fabien Le BrasDepartment of Hematology, Lymphoid Malignancies Unit, CHU Henri Mondor, Créteil, France.
Kamal BouabdallahHematology and Cellular Therapy Department, CHU Bordeaux, Bordeaux, France.
Fabien DespasHematology and Internal Medicine Department, Institut Universitaire du Cancer-Oncopole, CHU de Toulouse, Toulouse, France.
Jacques-Olivier BayHematology and Cellular Therapy Department, CHU de Clermont-Ferrand, Clermont-Ferrand, France.
Marie-Thérèse RubioDepartment of Hematology CHRU Nancy, biopole de l'Université de Lorraine, Nancy, France.
Mohamad MohtyHematology Department Saint-Antoine Hospital, Sorbonne University, Paris, France.
Olivier CasasnovasDepartment of Hematology and INSERM 1231, CHU Dijon Bourgogne, Dijon, France.ORCID 0000-0002-1156-8983
Sylvain ChoquetHematology Department, hôpital de la Pitié-Salpêtrière, Sorbonne Université, Paris, France.ORCID 0000-0002-7791-0470
Cristina Castilla-LlorenteHematology Department, Gustave Roussy Cancer Campus, Université Paris-Saclay, Villejuif, France.
Stéphanie GuidezHematology and Cellular Therapy Department, CHU de Poitiers, Poitiers, France.ORCID 0000-0001-8755-5591
Michaël LoschiHematology Department CHU de Nice, Université Cote d'Azur, Nice, France.ORCID 0000-0002-4460-5939
Blandine GuffroyDepartment of Hematology, Institut de Cancérologie Strasbourg Europe, Strasbourg, France.
Sylvain CarrasInstitute for Advanced Biosciences, Hematology Department CHU Grenoble-Alpes, University Grenoble-Alpes, Grenoble, France.ORCID 0000-0002-0796-7914
Laurianne Drieu La RochelleHematology and Cellular Therapy Department, CHU de Tours, Tours, France.
Mathilde GuilletThe Lymphoma Academic Research Organization, Statistics, Pierre-Bénite, France.
Roch HouotDepartment of Hematology, University Hospital of Rennes, UMR U1236 INSERM, University of Rennes, French Blood Establishment, Rennes, France.ORCID 0000-0003-1729-8213
Inserm · FRSorbonne Université · FRCentre Hospitalier Universitaire de Clermont-Ferrand · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de Montpellier · FRCentre Hospitalier Universitaire de Nantes · FRCentre Hospitalier Universitaire de Poitiers · FRCentre Hospitalier Universitaire de Rennes · FRCentre Hospitalier Universitaire de Toulouse · FRCentre Hospitalier Universitaire de Tours · FRCentre Hospitalier Universitaire Henri-Mondor · FRÉtablissement Français du Sang · FRHôpital Lyon Sud · FRHospices Civils de Lyon · FRInstitut de Cancérologie Strasbourg · FRUniversité Côte d'Azur · FRUniversité de Lille · FRUniversité de Lorraine · FRUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractChimeric antigen receptor (CAR) T-cells targeting CD19 have been approved for the treatment of relapse/refractory large B-cell lymphoma. Hematotoxicity is the most frequent CAR T-cell-related adverse event. Transfusion support is a surrogate marker of severe cytopenias. Transfusion affects patients' quality of life, presents specific toxicities, and is known to affect immunity through the so-called transfusion-related immunomodulation that may affect CAR T-cell efficacy. We analyzed data from 671 patients from the French DESCAR-T registry for whom exhaustive transfusion data were available. Overall, 401 (59.8%) and 378 (56.3%) patients received transfusion in the 6-month period before and after CAR T-cell infusion, respectively. The number of patients receiving transfusion and the mean number of transfused products increased during the 6-month period before CAR T-cell infusion, peaked during the first month after infusion (early phase), and decreased over time. Predictive factors for transfusion at the early phase were age >60 years, ECOG PS ≥2, treatment with axicabtagene ciloleucel, pre-CAR T-cell transfusions, and CAR-HEMATOTOX score ≥2. Predictive factors for late transfusion (between 1 and 6 months after infusion) were pre-CAR T-cell transfusions, CAR-HEMATOTOX score ≥2, ICANS ≥3 (for red blood cells [RBC] transfusion), and tocilizumab use (for platelets transfusion). Early transfusions and late platelets (but not RBC) transfusions were associated with a shorter progression-free survival and overall survival. Lymphoma-related mortality and nonrelapse mortality were both increased in the transfused population. Our data shed light on the mechanisms of early and late cytopenia and on the potential impact of transfusions on CAR T-cell efficacy and toxicity.

Indexed as

Immunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseAntigens, CD19BiomarkersHumansMiddle AgedNeoplasm Recurrence, LocalQuality of LifeAntigens, CD19Biomarkers

Identifiers

PMID38181767
PMCPMC10982963
OpenAlexW4390603623

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.