Evidence map›Paper›PMID 41115257›Full record

Trial reportJournal of clinical oncology : official journal of the American Society of Clinical Oncology2025

Efficacy and Safety of Glofitamab Plus Polatuzumab Vedotin in Relapsed/Refractory Large B-Cell Lymphoma Including High-Grade B-Cell Lymphoma: Results From a Phase Ib/II Trial.

Martin Hutchings, Anna Sureda, Francesc Bosch, Thomas Stauffer Larsen, Paolo Corradini, Abraham Avigdor, María José Terol, Antonio Rueda Dominguez, Antonio Pinto, Alan Skarbnik and 10 more

Registry-linked trialAbstract readClinical Trial, Phase IIClinical Trial, Phase IMulticenter Study
In one paragraph

Trial report in Journal of clinical oncology : official journal of the American Society of Clinical Oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03533283 (An Open-Label, Multi-Center, Phase IB/II Study of Glofitamab and Atezolizumab or Polatuzumab Vedotin), which is not on this map. 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.

NCT03533283 phase1 / phase2active not recruitingnot on this map

An Open-Label, Multi-Center, Phase IB/II Study of Glofitamab and Atezolizumab or Polatuzumab Vedotin (Plus a Single Pre-Treatment Dose of Obinutuzumab) in Adult Patients With Relapsed/Refractory B-Cell Non-Hodgkin's Lymphoma

TypeinterventionalSponsorHoffmann-La RocheRan2018 to 2026Enrolled211ConditionsNon-Hodgkins LymphomaArmsGlofitamab, Atezolizumab, Obinutuzumab, Tocilizumab, Polatuzumab Vedotin
3 · Its place in the literature

Who cites it

13 citing papers in PubMed.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Review
  12. Article
  13. Is less more? Revisiting elective nodal irradiation in head and neck cancer.Strahlentherapie und Onkologie : Organ der Deutschen Rontgengesellschaft ... [et al] · 2025
    Review
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.

Martin HutchingsRigshospitalet and University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-3873-1741
Anna SuredaClinical Hematology División, Institut Català d'Oncologia-L'Hospitalet, Institut d'Investigació Biomèdica de Bellvitge (IDIBELL), Universitat de Barcelona, Barcelona, Spain.ORCID 0000-0002-1238-6970
Francesc BoschUniversity Hospital Vall d'Hebron, Vall d'Hebron Institute of Oncology (VHIO), Barcelona, Spain.ORCID 0000-0001-9241-2886
Thomas Stauffer LarsenOdense University Hospital, Odense, Denmark.ORCID 0000-0002-8418-6708
Paolo CorradiniUniversity of Milano and Fondazione IRCCS Istituto Nazionale dei Tumori, Milano, Italy.ORCID 0000-0002-9186-1353
Abraham AvigdorSheba Medical Center, Ramat Gan and Tel Aviv University, Tel Aviv, Israel.
María José TerolHospital Clínico Universitario INCLIVA, University of Valencia, Valencia, Spain.ORCID 0000-0002-9467-932X
Antonio Rueda DominguezMedical Oncology Department, Virgen de la Victoria University Hospital, IBIMA-Bionand Platform, Málaga, Spain.ORCID 0000-0001-5890-0149
Antonio PintoIstituto Nazionale Tumori-IRCCS-Fondazione "G. Pascale", Naples, Italy.
Alan SkarbnikNovant Health Cancer Institute, Charlotte, NC.
Raul CordobaFundación Jiménez Díaz University Hospital, Madrid, Spain.ORCID 0000-0002-7654-8836
Judit Meszaros JørgensenAarhus University Hospital, Aarhus, Denmark.
Pier Luigi ZinzaniIRCCS Azienda Ospedaliero-Universitaria di Bologna Istituto di Ematologia Seràgnoli, Bologna, Italy.ORCID 0000-0002-2112-2651
Wilfred LeungGenentech Inc, South San Francisco, CA.
Alessia BottosF. Hoffmann-La Roche Ltd, Basel, Switzerland.ORCID 0000-0001-6311-2833
Donghang LiRoche (China) Holding Ltd, Shanghai, China.
James RelfRoche Products Ltd, Welwyn Garden City, United Kingdom.
Maneesh TandonRoche Products Ltd, Welwyn Garden City, United Kingdom.
Gila SellamF. Hoffmann-La Roche Ltd, Basel, Switzerland.
Giuseppe GrittiASST Ospedale Papa Giovanni XXIII, Bergamo, Italy.ORCID 0000-0002-6789-5123

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAn unmet need remains for more effective therapies for relapsed/refractory (R/R) large B-cell lymphoma (LBCL), especially high-grade B-cell lymphoma (HGBCL). We present the primary analysis of a phase Ib/II study (ClinicalTrials.gov identifier: NCT03533283) investigating efficacy and safety of glofitamab plus polatuzumab vedotin (Glofit-Pola) in patients with R/R LBCL, including HGBCL and those who received previous chimeric antigen receptor (CAR) T-cell therapy.

methodsPatients received 1,000 mg obinutuzumab on Cycle (C)1 Day (D)1 (once daily). Polatuzumab vedotin (1.8 mg/kg) was given on C1D2 and D1 of C2-6 (21-day cycles; once daily). Glofitamab was given as step-up doses in C1 (D8, 2.5 mg; D15, 10 mg) followed by 30 mg on D1 of C2-12 (21-day cycles; once daily). Polatuzumab vedotin was given for six fixed-duration cycles, and glofitamab for 12.

resultsAs of September 2, 2024, 129 patients with LBCL (HGBCL; n = 44, 34.1%), received ≥1 dose of study treatment. The median age was 67 years (range, 23-84), and 63.6% were male. Patients had received a median of 2 (range, 1-7) previous lines of treatment (previous CAR T-cell therapy, n = 28, 21.7%). The independent review committee-assessed overall response rate was 78.3% (complete response rate, 59.7%). The median progression-free survival and overall survival (OS) were 12.3 and 33.8 months, respectively (median OS follow-up time, 32.7 months). The most common adverse event (AE) was cytokine release syndrome (43.4%; grade 1-2: 41.9%; one grade 5 event). Grade 3-4 AEs occurred in 58.9% of patients; 9.3% had grade 5 AEs, and 14.7% discontinued treatment because of AEs.

conclusionGlofit-Pola demonstrated high efficacy and durable responses, with manageable safety, in heavily pretreated patients with R/R LBCL, including patients with HGBCL and previous CAR T-cell therapy failure.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsLymphoma, B-CellLymphoma, Large B-Cell, DiffuseNeoplasm Recurrence, LocalAdultAgedAged, 80 and overAntibodies, BispecificAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedFemaleHumansImmunoconjugatesMaleMiddle AgedNeoplasm GradingAntibodies, BispecificAntibodies, MonoclonalAntibodies, Monoclonal, HumanizedImmunoconjugatespolatuzumab vedotin

Identifiers

PMID41115257
PMCPMC12711264

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.