Evidence map›Paper›PMID 39747123›Full record

ArticleNature communications2025

Integrating genetic subtypes with PET scan monitoring to predict outcome in diffuse large B-cell lymphoma.

Matías S Mendeville, Jurriaan Janssen, G Tjitske Los-de Vries, Erik van Dijk, Julia Richter, Marcel Nijland, Margaretha G M Roemer, Phylicia Stathi, Nathalie J Hijmering, Reno Bladergroen and 15 more

Registry-linked trialAbstract read
In one paragraph

Article in Nature communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00544219 (Prospective Evaluation of the Predictive Value of PET in Patients With Diffuse Large B-cell-lymphoma Under R-CHOP-14. A Multicenter Study), which is not on this map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing 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.

NCT00544219 nacompletednot on this map

Prospective Evaluation of the Predictive Value of PET in Patients With Diffuse Large B-cell-lymphoma Under R-CHOP-14. A Multicenter Study

TypeinterventionalSponsorSwiss Cancer InstituteRan2007 to 2016Enrolled156ConditionsLymphomaArmsrituximab, cyclophosphamide, doxorubicin hydrochloride, prednisone, vincristine sulfate
3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

  1. Trial
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  7. Integration of [Leukemia · 2025
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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

25 authors.

Matías S Mendeville *Department of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Jurriaan Janssen *Department of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.ORCID 0000-0003-2536-7864
G Tjitske Los-de VriesDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Erik van DijkDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Julia RichterDepartment of Pathology, Hematopathology Section and Lymph Node Registry University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.ORCID 0000-0002-9543-4084
Marcel NijlandDepartment of Hematology University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.
Margaretha G M RoemerDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Phylicia StathiDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Nathalie J HijmeringDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Reno BladergroenDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Diego A PelazDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.ORCID 0009-0008-8395-2598
Arjan DiepstraDepartment of Pathology and Medical Biology University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.ORCID 0000-0001-9239-1050
Corinne J EertinkDepartment of Hematology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Coreline N BurggraaffDepartment of Hematology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Yongsoo KimDepartment of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.ORCID 0000-0002-2995-2131
Pieternella J LugtenburgDepartment of Hematology, Erasmus MC Cancer Institute, University Medical Center Rotterdam, Rotterdam, The Netherlands.
Anke van den BergDepartment of Pathology and Medical Biology University of Groningen, University Medical Centre Groningen, Groningen, the Netherlands.ORCID 0000-0002-8894-2638
Alexandar TzankovInstitute of Pathology, University of Basel and University Hospital Basel, Basel, Switzerland.ORCID 0000-0002-1100-3819
Stefan DirnhoferInstitute of Pathology, University of Basel and University Hospital Basel, Basel, Switzerland.
Ulrich DührsenDepartment of Hematology, University Hospital Essen, Essen, Germany.
Andreas HüttmannDepartment of Hematology, University Hospital Essen, Essen, Germany.ORCID 0000-0003-2230-3873
Wolfram KlapperDepartment of Pathology, Hematopathology Section and Lymph Node Registry University Hospital Schleswig-Holstein, Campus Kiel, Kiel, Germany.ORCID 0000-0001-7208-4117
Josée M ZijlstraDepartment of Hematology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.
Bauke Ylstra *Department of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands. b.ylstra@amsterdamumc.nl.ORCID 0000-0001-9479-3010
Daphne de Jong *Department of Pathology, Cancer Center Amsterdam, Amsterdam UMC, location VUmc, Amsterdam, The Netherlands.ORCID 0000-0002-9725-4060

Funding

KWF Kankerbestrijding (Dutch Cancer Society) KWF 2012-5711KWF Kankerbestrijding (Dutch Cancer Society) KWF 2013-6269KWF Kankerbestrijding (Dutch Cancer Society) KWF 2015-7925
6 · The paper itself

Abstract

Next Generation Sequencing-based subtyping and interim- and end of treatment positron emission tomography (i/eot-PET) monitoring have high potential for upfront and on-treatment risk assessment of diffuse large B-cell lymphoma patients. We performed Dana Farber Cancer Institute (DFCI) and LymphGen genetic subtyping for the HOVON84 (n = 208, EudraCT-2006-005174-42) and PETAL (n = 204, EudraCT-2006-001641-33) trials retrospectively combined with DFCI genetic data (n = 304). For all R-CHOP treated patients (n = 592), C5/MCD- and C2/A53-subtypes show significantly worse outcome independent of the international prognostic index. For all subtypes, adverse prognostic value of i/eot-PET-positive status is confirmed. Consistent with frequent primary refractory disease, only 67% C2 patients become eot-PET-negative versus 81-88% for other subtypes. Indicative of high relapse rates, outcome of C5 i/eot-PET-negative patients remains significantly worse in HOVON-84, which trend validates in the PETAL and SAKK38-07 trials (NCT00544219). These results show the added value of integrated genetic subtyping and PET monitoring for prognostic stratification and subtype-specific trial design.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsCyclophosphamideLymphoma, Large B-Cell, DiffusePositron-Emission TomographyPrednisoneRituximabVincristineAdultAgedDoxorubicinFemaleHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedPrognosisCyclophosphamideDoxorubicinPrednisoneR-CHOP protocolRituximabVincristine

Identifiers

PMID39747123
PMCPMC11696268

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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.