Evidence map›Paper›PMID 42636799›Full record

ArticleCell reports. Medicine2026

Cell-free DNA genomic and fragmentomic features for early outcome prediction in large B cell lymphoma.

Steven Wang, Parisa Mapar, Norbert Moldovan, Ymke van der Pol, Aram Safrastyan, Erik van Werkhoven, Normastuti Adhini Tantyo, Bart Snieder, André F Do Brito Valente, A Vera de Jonge and 26 more

Abstract read
In one paragraph

Article in Cell reports. Medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

36 authors.

Steven WangAmsterdam UMC Location Vrije Universiteit Amsterdam, Hematology, Amsterdam, the Netherlands; Amsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands; Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, the Netherlands.
Parisa MaparAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands; Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, the Netherlands; Institute for Molecular Medicine Finland (FIMM), HiLIFE, University of Helsinki, Helsinki, Finland.
Norbert MoldovanAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands; Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, the Netherlands.
Ymke van der PolAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands; Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, the Netherlands.
Aram SafrastyanCancer Research UK National Biomarker Centre, University of Manchester, Manchester, UK.
Erik van WerkhovenHemato-Oncology Foundation for Adults in the Netherlands (HOVON), Rotterdam, the Netherlands.
Normastuti Adhini TantyoAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands.
Bart SniederAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands.
André F Do Brito ValenteAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands.
A Vera de JongeAmsterdam UMC Location Vrije Universiteit Amsterdam, Hematology, Amsterdam, the Netherlands.
Avinash DinmohamedNetherlands Comprehensive Cancer Organization (IKNL), Utrecht, the Netherlands.
Esther E E DreesAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands; Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, the Netherlands.
Margaretha G M RoemerAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands; Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, the Netherlands.
Bauke YlstraAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands; Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, the Netherlands.
Clara P W KlerkDijklander Hospital, Hoorn, the Netherlands.
Leonie StrobbeGelre Ziekenhuis, Zutphen, the Netherlands.
Yorick SandbergMaasstad Ziekenhuis, Rotterdam, the Netherlands.
Rinske S BoersmaAmphia Ziekenhuis, Breda, the Netherlands.
Harry KoeneSt. Antonius Ziekenhuis, Nieuwegein, the Netherlands.
Hans PruijtJeroen Bosch Ziekenhuis, 's-Hertogenbosch, the Netherlands.
Koen de HeerFlevoziekenhuis, Almere, the Netherlands.
Rozemarijn van RijnMedical Center Leeuwarden, Leeuwarden, the Netherlands.
Yavuz M BilginAdrz, Goes, the Netherlands.
Eva de JonghAlbert Schweitzer Ziekenhuis, Dordrecht, the Netherlands.
Marcel NijlandUniversity Medical Center Groningen, Groningen, the Netherlands.
Marjolein van der PoelMaastricht University Medical Center, Maastricht, the Netherlands.
Ad KosterVieCuri Medical Center, Venlo, the Netherlands.
Laurens NieuwenhuizenMaxima Medical Center, Eindhoven, the Netherlands.
Rob FijnheerMeander Medical Center, Amersfoort, the Netherlands.
Aart BeekerSpaarne Gasthuis, Hoofddorp, the Netherlands.
Rogier MousUniversity Medical Center Utrecht, Utrecht, the Netherlands.
Vibeke K J VergoteUniversity Hospitals Leuven, Leuven, Belgium.
Joost S P VermaatLeiden University Medical Center, Leiden, the Netherlands.
D Michiel PegtelAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands; Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, the Netherlands.
Martine E D ChamuleauAmsterdam UMC Location Vrije Universiteit Amsterdam, Hematology, Amsterdam, the Netherlands; Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, the Netherlands.
Florent MouliereAmsterdam UMC Location Vrije Universiteit Amsterdam, Pathology, Amsterdam, the Netherlands; Cancer Center Amsterdam, Imaging and Biomarkers, Amsterdam, the Netherlands; Cancer Research UK National Biomarker Centre, University of Manchester, Manchester, UK. Electronic address: florent.mouliere@cruk.manchester.ac.uk.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Curative-intent immunochemotherapy fails in ∼30% of patients with large B cell lymphoma (LBCL), yet no validated molecular tool enables early identification of high-risk individuals to guide treatment intensification. Using shallow whole-genome sequencing (sWGS) of plasma cell-free DNA from 190 LBCL patients, we develop and validate the ACT score (aberrations, composition of fragments, and terminal motif analyses), a composite classifier integrating genomic and fragmentomic features from a single post-cycle-1 sample. ACT-positive patients have worse 2-year outcomes versus ACT-negative patients: time-to-progression 29% vs. 83% (hazard ratio [HR]: 4.4, 95% confidence interval [CI]: 1.9-10.0; p = 1.5 × 10

Indexed as

Cell-Free Nucleic AcidsGenomicsLymphoma, Large B-Cell, DiffuseAgedBiomarkers, TumorFemaleHumansMaleMiddle AgedPrognosisWhole Genome SequencingBiomarkers, TumorCell-Free Nucleic Acidscell-free DNAfragmentomicslarge B cell lymphomaliquid biopsymultimodalrisk stratificationshallow whole-genome sequencing

Identifiers

PMID42636799
PMCPMC13589503

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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.