Evidence map›Paper›PMID 40249860›Full record

Trial reportBlood advances2025

Atezolizumab consolidation in patients with high-risk diffuse large B-cell lymphoma in complete remission after R-CHOP.

Marcel Nijland, Djamila E Issa, Johanna A A Bult, Dries Deeren, Gerjo A Velders, Marten R Nijziel, Yorick Sandberg, Vibeke Vergote, Margriet Oosterveld, Rob Fijnheer and 32 more

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

Trial report in Blood advances, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03463057 (A Phase II Study Evaluating the Feasibility and Clinical Efficacy of Atezolizumab Consolidation Treatment in High Risk Diffuse Large B-cell Lymphoma), which is not on this map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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.

NCT03463057 phase2active not recruitingnot on this map

A Phase II Study Evaluating the Feasibility and Clinical Efficacy of Atezolizumab Consolidation Treatment in High Risk Diffuse Large B-cell Lymphoma

TypeinterventionalSponsorStichting Hemato-Oncologie voor Volwassenen NederlandRan2018 to 2027Enrolled109ConditionsNHL, DLBCLArmsAtezolizumab
3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Prospective Validation of Circulating Tumor DNA Measurable Residual Disease After First-Line Therapy in Large B-Cell Lymphoma.Journal of clinical oncology : official journal of the American Society of Clinical Oncology · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. 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

42 authors.

Marcel NijlandDepartment of Hematology, University Medical Center Groningen, Groningen, The Netherlands.ORCID 0000-0002-2740-2873
Djamila E IssaDepartment of Hematology, Jeroen Bosch Hospital, Den Bosch, The Netherlands.ORCID 0000-0002-4512-7019
Johanna A A BultDepartment of Hematology, University Medical Center Groningen, Groningen, The Netherlands.ORCID 0009-0000-6090-4448
Dries DeerenDepartment of Hematology, Academic Hospital Delta, Roeselare, Belgium.ORCID 0000-0001-9599-2142
Gerjo A VeldersDepartment of Hematology, Gelderse Vallei Hospital, Ede, The Netherlands.
Marten R NijzielDepartment of Hematology, Catharine Hospital, Eindhoven, The Netherlands.ORCID 0000-0001-9069-4939
Yorick SandbergDepartment of Hematology, Maasstad Hospital, Rotterdam, The Netherlands.ORCID 0000-0001-8716-0856
Vibeke VergoteDepartment of Hematology, University Hospital Leuven, Leuven, Belgium.
Margriet OosterveldDepartment of Hematology, Canisius Wilhelmina Hospital, Nijmegen, The Netherlands.ORCID 0000-0002-6742-9261
Rob FijnheerDepartment of Hematology, Meander Medical Center, Amersfoort, The Netherlands.
Rolf E BrouwerDepartment of Hematology, Reinier de Graaf Hospital, Delft, The Netherlands.
Rinske S BoersmaDepartment of Hematology, Amphia Hospital, Breda, The Netherlands.
Kalung WuDepartment of Hematology, Hospital Network Antwerpen Stuiverberg, Antwerp, Belgium.
Laurens NieuwenhuizenDepartment of Hematology, Maxima Medical Center, Eindhoven, The Netherlands.
Joost S P VermaatDepartment of Hematology, Leiden University Medical Center, Leiden, The Netherlands.ORCID 0000-0002-1628-6256
Roel J W van KampenDepartment of Hematology, Zuyderland Medical Center, Sittard-Geleen, The Netherlands.
Wim E TerpstraDepartment of Hematology, Onze Lieve Vrouwe Gasthuis, Amsterdam, The Netherlands.
Sylvia SnauwaertDepartment of Hematology, General Hospital Sint-Jan Brugge, Bruges, Belgium.
Marjolein W van der PoelDepartment of Hematology, Maastricht University Medical Center, Maastricht, The Netherlands.
Eva de JonghDepartment of Hematology, Albert Schweitzer Hospital, Dordrecht, The Netherlands.
Marc F DurianDepartment of Hematology, Elisabeth-TweeSteden Hospital, Tilburg, The Netherlands.ORCID 0009-0008-8810-5187
Leonie StrobbeDepartment of Hematology, Gelre Hospital, Apeldoorn, The Netherlands.
Aart BeekerDepartment of Hematology, Spaarne Gasthuis Hospital, Haarlem, The Netherlands.ORCID 0000-0003-4133-769X
Alain GadisseurDepartment of Hematology, University Medical Center Antwerpen, Edegem, Belgium.
Roos S van RijnDepartment of Hematology, Medical Center Leeuwarden, Leeuwarden, The Netherlands.
Otto VisserDepartment of Hematology, Isala Hospital, Zwolle, The Netherlands.
Jeanette K DoorduijnDepartment of Hematology, Erasmus Medical Center Cancer Institute, Rotterdam, The Netherlands.ORCID 0000-0002-1014-0918
Tjeerd J F SnijdersDepartment of Hematology, Medisch Spectrum Twente, Enschede, The Netherlands.
Matthijs H SilbermannDepartment of Hematology, Tergooi Hospital, Hilversum, The Netherlands.
Daphne de JongDepartment of Pathology and Medical Biology, University Medical Center Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-9725-4060
Martine ChamuleauDepartment of Hematology, University Medical Center Amsterdam, Amsterdam, The Netherlands.
Rogier MousDepartment of Hematology, University Medical Center Utrecht, Utrecht, The Netherlands.
Hilde JalvingDepartment of Oncology, University Medical Center Groningen, Groningen, The Netherlands.
Heleen Visser-WisselaarHemato Oncology Foundation for Adults in The Netherlands, Clinical Operations, Rotterdam, The Netherlands.
Sonja Jansen van de BerghHemato Oncology Foundation for Adults in The Netherlands, Clinical Operations, Rotterdam, The Netherlands.
Gerben J C ZwezerijnenDepartment of Radiology, Amsterdam University Medical Center, Cancer Center Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0002-9571-9362
Edwin BremerDepartment of Hematology, University Medical Center Groningen, Groningen, The Netherlands.
Mirian BrinkDepartment of Research and Development, Netherlands Comprehensive Cancer Organization, Utrecht, The Netherlands.ORCID 0000-0002-6014-4810
Arjan DiepstraDepartment of Pathology and Medical Biology, University Medical Center Groningen, Groningen, The Netherlands.
Dana A ChituDepartment of Hematology, Erasmus Medical Center Cancer Institute, Rotterdam, The Netherlands.
Harry R KoeneDepartment of Hematology, Antonius Hospital, Nieuwegein, The Netherlands.
Josée M ZijlstraDepartment of Hematology, University Medical Center Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0003-1074-5922

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractThe risk of relapse among high-risk patients with diffuse large B-cell lymphoma (DLBCL) in complete metabolic remission (CMR) after rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP) therapy is 20% to 25%. Here, we evaluated whether consolidation with the programmed cell death ligand 1 checkpoint inhibitor atezolizumab could reduce the relapse risk. In this phase 2, open-label trial, patients with DLBCL with an International Prognostic Index (IPI) score of ≥3 and CMR after R-CHOP received 1200 mg atezolizumab every 3 weeks for 18 cycles. The primary end point was disease-free survival (DFS) at 2 years, with the aim of improving it to 89% compared to historical 79%. Secondary end points included overall survival (OS) and safety (Common Terminology Criteria for Adverse Events version 4.0). Analyses were on an intention-to-treat principle. Of 109 patients, 65% completed treatment. The cohort was 59% males, with 63% having high-intermediate risk IPI scores. At a median follow-up of 36.4 months, 15 relapses occurred (median, 8.2 months). The 2-year DFS was 87.9% (90% confidence interval [CI], 81.5-92.1), and the 2-year OS was 96.3% (90% CI, 91.7-98.3), meeting the primary objective. Treatment with salvage chemotherapy resulted in 10 of 13 patients achieving a second CMR. OS was significantly better among atezolizumab-treated patients than in a population-based matched control cohort from the Netherlands Cancer Registry. Adverse events (AEs) affected 79% of patients, with 18% developing immune-related AEs, including 4.5% grade 3 to 4. Atezolizumab consolidation significantly improved DFS in high-risk patients with DLBCL compared to historical cohorts. OS was significantly better than a population-based control cohort. These findings warrant further validation and assessment of immune checkpoint inhibitors as consolidation strategy in DLBCL. This trial was registered at www.clinicaltrials.gov as #NCT03463057.

Indexed as

Antibodies, Monoclonal, HumanizedAntineoplastic Combined Chemotherapy ProtocolsLymphoma, Large B-Cell, DiffuseAdultAgedAged, 80 and overConsolidation ChemotherapyCyclophosphamideDoxorubicinFemaleHumansMaleMiddle AgedPathologic Complete ResponsePrednisoneRemission InductionAntibodies, Monoclonal, HumanizedatezolizumabCyclophosphamideDoxorubicinPrednisoneR-CHOP protocolRituximabVincristine

Identifiers

PMID40249860
PMCPMC12274673

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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.