Evidence map›Paper›PMID 39968186›Full record

ArticleHemaSphere2025

Outcomes of patients with relapsed or refractory primary mediastinal B-cell lymphoma treated with anti-CD19 CAR-T cells: CARTHYM, a study from the French national DESCAR-T registry.

Jean Galtier, Charles Mesguich, Pierre Sesques, Vivien Dupont, Emmanuel Bachy, Roberta Di Blasi, Catherine Thieblemont, Thomas Gastinne, Guillaume Cartron, Gabriel Brisou and 17 more

Erratum issuedAbstract read
In one paragraph

Article in HemaSphere, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Standardized FDG-PET interpretation during CAR T-cell therapy in R/R DLBCL: a DESCAR-T study.European journal of nuclear medicine and molecular imaging · 2026
    Article
  2. Observational
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Review
  10. Observational
  11. Article
  12. Article
  13. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors.

Jean GaltierCHU de Bordeaux, Service d'hématologie Clinique et de thérapie cellulaire Bordeaux France.ORCID 0000-0002-2176-227X
Charles MesguichCHU de Bordeaux, Service de médecine nucléaire Bordeaux France.
Pierre SesquesHospices civils de Lyon, Service d'hématologie clinique Lyon France.
Vivien DupontLYSARC, Département de biostatistiques Lyon France.
Emmanuel BachyHospices civils de Lyon, Service d'hématologie clinique Lyon France.
Roberta Di BlasiHôpital Saint-Louis, Service d'hématologie clinique, Assistance publique - Hôpitaux de Paris Paris France.
Catherine ThieblemontHôpital Saint-Louis, Service d'hématologie clinique, Assistance publique - Hôpitaux de Paris Paris France.
Thomas GastinneCHU de Nantes, Service d'hématologie clinique Nantes France.
Guillaume CartronCHU de Montpellier, Service d'hématologie clinique Montpellier France.
Gabriel BrisouInstitut Paoli Calmettes, Service d'hématologie clinique Marseille France.
François-Xavier GrosCHU de Bordeaux, Service d'hématologie Clinique et de thérapie cellulaire Bordeaux France.
Justine DecroocqHôpital Cochin, Service d'hématologie clinique, Asistance publique - Hôpitaux de Paris Paris France.
Franck MorschhauserCHRU de Lille, Service d'hématologie clinique Lille France.
Marie-Thérèse RubioCHRU de Nancy, Service d'hématologie clinique Nancy France.
Laurianne Drieu La RochelleCHU de Tours, Service d'hématologie clinique Tours France.
Fabien Le BrasHôpital Henri Mondor, Service d'hématologie clinique, Assistance publique - Hôpitaux de Paris Paris France.
Sylvain CarrasCHU de Grenoble, Service d'hématologie clinique Grenoble France.
Adrien ChauchetCHU de Besançon, Service d'hématologie clinique Bensaçon France.
Jacques-Olivier BayCHU de Clermont-Ferrand, Service d'hématologie clinique Clermont-Ferrand France.
Magalie JorisCHU d'Amiens, Service d'hématologie clinique Amiens France.
Mickael LoschiCHU de Nice, Service d'hématologie clinique Nice France.
Aline Tanguy-SchmidtCHU d'Angers, Service d'hématologie clinique Angers France.
Alexandra MarquetLYSARC Lyon France.
Vincent CamusDépartement d'Hématologie Centre Henri Becquerel Rouen France.ORCID 0000-0002-1559-007X
Steven Le GouillInstitut Curie, Service d'hématologie clinique Paris France.
Roch HouotCHU de Rennes, Service d'hématologie clinique Rennes France.
Krimo BouabdallahCHU de Bordeaux, Service d'hématologie Clinique et de thérapie cellulaire Bordeaux France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Primary mediastinal B-cell lymphoma (PMBL) is often cured with dose-dense anthracycline-based regimens but the prognosis at relapse or progression remains poor. While anti-CD19 CAR-T cell therapy has dramatically improved outcomes in relapsed or refractory large B-cell lymphoma, far less is known about their efficacy in PMBL. Using the systematic record of all patients treated with CAR-T cells prospectively included in the DESCAR-T registry in France, along with centrally reviewed positon-emission tomography (PET) imaging, we describe the outcomes and key determinants of treatment success in PMBL patients treated over a 6-year period. Among 82 patients infused in the registry we observed a best complete response (CR) rate, 2-year progression-free survival (PFS), and 2-year overall survival (OS) of 68.1%, 57.4%, and 73.8%, respectively. Outcomes were even better for the 62 patients infused with axicabtagene ciloleucel, with best CR rate, 2-year PFS, and 2-year OS reaching 74.5%, 70.4%, and 86.9%, respectively. Achieving a Deauville score of 1-4 or a ΔSUVmax reduction of more than 24% at the 1-month evaluation was associated with excellent outcomes, whereas increased total metabolic tumor volume baseline PET increased the risk of treatment failure. Surprisingly, neither the response to bridging therapy nor the type of bridging therapy (chemotherapy versus immune checkpoint inhibitors) were associated with long-term outcomes. In conclusion, this study confirms that anti-CD19 CAR-T cells as a valid standard-of-care for relapsed and refractory PMBL and highlights key determinants of treatment success.

Identifiers

PMID39968186
PMCPMC11833168

What OpenQuestion holds

Textmetadata
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.