Evidence map›Paper›PMID 33739857›Full record

ArticleJournal of clinical oncology : official journal of the American Society of Clinical Oncology2021

Glofitamab, a Novel, Bivalent CD20-Targeting T-Cell-Engaging Bispecific Antibody, Induces Durable Complete Remissions in Relapsed or Refractory B-Cell Lymphoma: A Phase I Trial.

Martin Hutchings, Franck Morschhauser, Gloria Iacoboni, Carmelo Carlo-Stella, Fritz C Offner, Anna Sureda, Gilles Salles, Joaquín Martínez-Lopez, Michael Crump, Denise N Thomas and 13 more

Open access · hybridAbstract readClinical Trial, Phase IMulticenter Study
In one paragraph

Article in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 262 papers, 8 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
262citing papers in PubMed, 8 pooled it
27.9field-weighted citation impact, top 1% 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

262 citing papers in PubMed, 8 syntheses or guidelines pooled it, 395 citations in OpenAlex.

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  15. Glofitamab in Relapsed/Refractory Mantle Cell Lymphoma: Results From a Phase I/II Study.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2025
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202 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

23 authors at 14 institutions in 11 countries.

Martin HutchingsDepartment of Hematology and Phase 1 Unit, Rigshospitalet, Copenhagen, Denmark.ORCID 0000-0003-3873-1741
Franck MorschhauserUniversité de Lille, CHU Lille, ULR 7365 - GRITA - Groupe de Recherche sur les formes Injectables et les Technologies Associées, Lille, France.
Gloria IacoboniDepartment of Hematology, Vall d'Hebron University Hospital, Experimental Hematology, Vall d'Hebron Institute of Oncology (VHIO), Vall d'Hebron Barcelona Hospital Campus, Barcelona, Spain.ORCID 0000-0003-0805-9288
Carmelo Carlo-StellaHumanitas Clinical and Research Center-IRCCS and Humanitas University, Rozzano, Italy.ORCID 0000-0003-3144-0124
Fritz C OffnerGhent University, Ghent, Belgium.
Anna SuredaInstitut Català d'Oncologia-Hospitalet, Institut d'Investigació Biomedica de Bellvitge, Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0002-1238-6970
Gilles SallesHôpital Lyon Sud, Université Claude Bernard Lyon 1, Pierre-Bénite, France.ORCID 0000-0002-9541-8666
Joaquín Martínez-LopezHospital 12 de Octubre, i+12, Complutense University, Centro Nacional de Investigaciones Oncológicas, CRIS Unit, Madrid, Spain.
Michael CrumpPrincess Margaret Cancer Centre, University Health Network, University of Toronto, Toronto, Canada.
Denise N ThomasRoche Innovation Center New York, Roche Pharma Research and Early Development, New York, NY.
Peter N MorcosRoche Innovation Center New York, Roche Pharma Research and Early Development, New York, NY.
Cristiano FerliniRoche Innovation Center New York, Roche Pharma Research and Early Development, New York, NY.
Ann-Marie E BröskeRoche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
Anton BelousovRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Zurich, Switzerland.
Marina BacacRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Zurich, Switzerland.
Natalie DimierRoche Innovation Center Welwyn, Roche Pharma Research and Early Development, Welwyn Garden City, United Kingdom.
David J CarlileRoche Innovation Center Welwyn, Roche Pharma Research and Early Development, Welwyn Garden City, United Kingdom.
Linda LundbergRoche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.
David Perez-CallejoRoche Innovation Center Basel, Roche Pharma Research and Early Development, Basel, Switzerland.
Pablo UmañaRoche Innovation Center Zurich, Roche Pharma Research and Early Development, Zurich, Switzerland.
Tom MooreRoche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
Martin WeisserRoche Innovation Center Munich, Roche Pharma Research and Early Development, Penzberg, Germany.
Michael J DickinsonPeter MacCallum Cancer Centre, Royal Melbourne Hospital, The University of Melbourne, Melbourne, Australia.ORCID 0000-0002-1492-5966
Roche (Switzerland) · CHLa Roche College · USRoche Pharma AG (Germany) · DERoche (United Kingdom) · GBGhent University Hospital · BEHumanitas University · ITInstitut d'Investigació Biomédica de Bellvitge · ESRigshospitalet · DKSpanish National Cancer Research Centre · ESThe Royal Melbourne Hospital · AUUniversitat Autònoma de Barcelona · ESUniversité Claude Bernard Lyon 1 · FRUniversité de Lille · FRUniversity Health Network · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeGlofitamab is a T-cell-engaging bispecific antibody possessing a novel 2:1 structure with bivalency for CD20 on B cells and monovalency for CD3 on T cells. This phase I study evaluated glofitamab in relapsed or refractory (R/R) B-cell non-Hodgkin lymphoma (B-NHL). Data for single-agent glofitamab, with obinutuzumab pretreatment (

methodsSeven days before the first dose of glofitamab (0.005-30 mg), all patients received 1,000 mg

resultsFollowing initial single-patient cohorts, 171 patients were treated within conventional multipatient cohorts and received at least one dose of glofitamab. This trial included heavily pretreated patients with R/R B-NHL; most were refractory to prior therapy (155; 90.6%) and had received a median of three prior therapies. One hundred and twenty-seven patients (74.3%) had diffuse large B-cell lymphoma, transformed follicular lymphoma, or other aggressive histology, and the remainder had indolent lymphoma subtypes. Five (2.9%) patients withdrew from treatment because of adverse events. Cytokine release syndrome occurred in 86 of 171 (50.3%) patients (grade 3 or 4: 3.5%); two (1.2%) patients experienced grade 3, transient immune effector cell-associated neurotoxicity syndrome-like symptoms. The overall response rate was 53.8% (complete response [CR], 36.8%) among all doses and 65.7% (CR, 57.1%) in those dosed at the recommended phase II dose. Of 63 patients with CR, 53 (84.1%) have ongoing CR with a maximum of 27.4 months observation.

conclusionIn patients with predominantly refractory, aggressive B-NHL, glofitamab showed favorable activity with frequent and durable CRs and a predictable and manageable safety profile.

Indexed as

AdultAgedAged, 80 and overAntibodies, BispecificAntigens, CD20Antineoplastic Agents, ImmunologicalFemaleHumansLymphoma, B-CellMaleMiddle AgedT-LymphocytesYoung AdultAntibodies, BispecificAntigens, CD20Antineoplastic Agents, Immunological

Identifiers

PMID33739857
PMCPMC8210975
OpenAlexW3137447968

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.