Evidence map›Paper›PMID 40181090›Full record

Trial reportNature cancer2025

Glofitamab in refractory or relapsed diffuse large B cell lymphoma after failing CAR-T cell therapy: a phase 2 LYSA study.

Guillaume Cartron, Roch Houot, Yassine Al Tabaa, Fabien Le Bras, Loïc Ysebaert, Sylvain Choquet, Fabrice Jardin, Jacques-Olivier Bay, François-Xavier Gros, Franck Morschhauser and 13 more

Registry-linked trialAbstract readClinical Trial, Phase II
PubMed Publisher
In one paragraph

Trial report in Nature cancer, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04703686 (A Phase II Trial Evaluating Glofitamab, a Bispecific CD3xCD20 Antibody for Relapse/Refractory Lymphomas After CAR T-cells Therapy), which is not on this map. Cited by 28 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed, 3 pooled it
–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.

NCT04703686 phase2completednot on this map

A Phase II Trial Evaluating Glofitamab, a Bispecific CD3xCD20 Antibody for Relapse/Refractory Lymphomas After CAR T-cells Therapy

TypeinterventionalSponsorThe Lymphoma Academic Research OrganisationRan2021 to 2025Enrolled67ConditionsDiffuse Large B-Cell Lymphoma Refractory, Refractory Indolent Adult Non-Hodgkin Lymphoma, Refractory Transformed B-cell Non-Hodgkin Lymphoma, Refractory Primary Mediastinal Large B-Cell Cell LymphomaArmsObinutuzumab, RO7082859
3 · Its place in the literature

Who cites it

28 citing papers in PubMed, 3 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Trial
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. Article
  18. Article
  19. Review
  20. 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

23 authors.

Guillaume CartronDepartment of Hematology, University Hospital of Montpellier, Montpellier, France. g-cartron@chu-montpellier.fr.ORCID http://orcid.org/0000-0003-0659-9635
Roch HouotDepartment of Hematology, University Hospital of Rennes, Rennes, France.ORCID http://orcid.org/0000-0003-1729-8213
Yassine Al TabaaScintidoc Nuclear Medicine Center, Clinique Clémentville, Montpellier, France.
Fabien Le BrasDepartment of Hematology, Lymphoma Malignancies Unit, Henri Mondor Hospital, Assistance Publique-Hôpitaux de Paris, Créteil, France.
Loïc YsebaertDepartment of Hematology, Cancer University Institute of Toulouse Oncopole, Toulouse, France.
Sylvain ChoquetDepartment of Hematology, La Pitié Salpetrière Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.ORCID http://orcid.org/0000-0002-7791-0470
Fabrice JardinDepartment of Hematology, U1245, Henri Becquerel Institute, Rouen, France.ORCID http://orcid.org/0000-0002-6804-7943
Jacques-Olivier BayDepartment of Adults Cell Therapy and Clinical Hematology, University Hospital Clermont-Ferrand, Clermont-Ferrand, France.ORCID http://orcid.org/0000-0002-7032-5180
François-Xavier GrosDepartment of Clinical Hematology and Cell Therapy, University Hospital of Bordeaux, Bordeaux, France.ORCID http://orcid.org/0000-0001-8998-3039
Franck MorschhauserDepartment of Hematology, University Hospital of Lille, Lille, France.
Olivier CasasnovasDepartment of Hematology, University Hospital Dijon Bourgogne, Dijon, France.
Thomas GastinneDepartment of Hematology, University Hospital, Nantes, France.
Catherine ThieblemontDepartment of Onco-Hematology, Saint Louis Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.ORCID http://orcid.org/0000-0002-9941-2448
Magalie JorisDepartment of Hematology, University Hospital of Amiens, Amiens, France.
Laure RicardDepartment of Hematology, Saint Antoine Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.
Caroline RegnyDepartment of Hematology, University Hospital of Grenoble, Grenoble, France.
Laurianne Drieu La RochelleDepartment of Hematology, University Hospital of Tours, Tours, France.
Pierre FeugierDepartment of Hematology, University Hospital of Nancy, Nancy, France.
Ambroise MarcaisDepartment of Hematology, Necker Hospital, Assistance Publique-Hôpitaux de Paris, Paris, France.ORCID http://orcid.org/0000-0002-6844-7920
Samuel GrioletDepartment of Biostatistics, LYSARC, Lyon-Sud Hospital, Pierre-Bénite, France.
Karin TarteUMR1236, SITI Laboratory, University Hospital, INSERM, EFS, Rennes, France.ORCID http://orcid.org/0000-0002-6809-917X
Camille LaurentDepartment of Pathology, Cancer University Institute of Toulouse Oncopole, Toulouse, France.
Pierre SesquesDepartment of Hematology, University Hospital of Lyon, Lyon, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Persons with diffuse large B cell lymphoma (DLBCL) refractory or in first progression/relapsed (R/R) after chimeric antigen receptor T (CAR-T) cell therapy exhibit dramatic outcomes. We enrolled such persons in a phase 2 single-arm, nonblinded trial ( NCT04703686 ) to evaluate the efficacy and safety of glofitamab, a CD20-CD3 T cell-engaging bispecific antibody, using a short ramp-up regimen to reach full dose within 1 week. A total of 46 participants received at least one glofitamab infusion following obinutuzumab (anti-CD20 monoclonal antibody) pretreatment. The primary endpoint was overall survival (OS). Secondary endpoints included independent-assessed best overall metabolic response rate (OMRR) and complete metabolic response rate (CMRR), progression-free survival (PFS), duration of response, safety and tolerability and health-related quality of life. After a median follow-up of 15.3 months (95% confidence interval (CI), 10.1-17.7), the primary endpoint was met, achieving a median OS of 14.7 months (90% CI, 8.8-not reached). The best OMRR was 76.1%. The best CMRR was 45.7%. The median PFS was 3.8 months (95% CI, 2.4-19.6). Despite the shortened setup dosing, no excess cytokine release syndrome or neurotoxicity events were observed (grade ≥ 3, 0% for both). In conclusion, glofitamab improved OS in participants with R/R DLBCL after CAR-T cell therapy, with a favorable safety profile.

Indexed as

Antibodies, BispecificImmunotherapy, AdoptiveLymphoma, Large B-Cell, DiffuseNeoplasm Recurrence, LocalAdultAgedAged, 80 and overAntibodies, Monoclonal, HumanizedFemaleHumansMaleMiddle AgedQuality of LifeReceptors, Chimeric AntigenAntibodies, BispecificAntibodies, Monoclonal, HumanizedobinutuzumabReceptors, Chimeric Antigen

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.