Evidence map›Paper›PMID 41047873›Full record

ArticleThe Journal of pathology2025

Mutation profiling in differential diagnosis between TdT-positive high-grade/large B-cell lymphoma and B-lymphoblastic leukaemia/lymphoma.

Maria-Myrsini Tzioni, Francesco Cucco, Lívia Rásó-Barnett, Zi Chen, Andrew Wotherspoon, Katrin S Kurz, Ewelina Madej, Jasmine Makker, Anna E Strazda, Fang Guo and 18 more

Abstract read
In one paragraph

Article in The Journal of pathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

28 authors.

Maria-Myrsini TzioniDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID https://orcid.org/0000-0001-9298-2045
Francesco CuccoDepartment of Pathology, University of Cambridge, Cambridge, UK.
Lívia Rásó-BarnettThe Haematopathology and Oncology Diagnostic Service, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Zi ChenDepartment of Pathology, University of Cambridge, Cambridge, UK.
Andrew WotherspoonDepartment of Histopathology, The Royal Marsden Hospital, London, UK.
Katrin S KurzDepartment of Clinical Pathology, Robert-Bosch-Krankenhaus, and Dr. Margarete Fischer-Bosch Institute for Clinical Pharmacology, Stuttgart, Germany.
Ewelina MadejDepartment of Pathology, University of Cambridge, Cambridge, UK.
Jasmine MakkerDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID https://orcid.org/0000-0002-5519-3351
Anna E StrazdaDepartment of Pathology, University of Cambridge, Cambridge, UK.
Fang GuoDepartment of Pathology, University of Cambridge, Cambridge, UK.
Caoimhe EganThe Haematopathology and Oncology Diagnostic Service, Cambridge University Hospitals NHS Foundation Trust, Cambridge, UK.
Elizabeth SoilleuxDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID https://orcid.org/0000-0002-4032-7249
Liz HookDepartment of Pathology, University of Cambridge, Cambridge, UK.
Laszlo KrenacsLaboratory of Tumor Pathology and Molecular Diagnostics, Szeged, Hungary.
Julia T GeyerDepartment of Pathology and Laboratory Medicine, Weill Cornell Medical College, New York, NY, USA.
Camille LaurentDepartment of Bio-Pathology, Institut Universitaire Cancer-Oncopole, Centre de Recherches en Cancérologie de Toulouse INSERM U1037, Toulouse, France.
Luc XerriDepartment of Pathology, Institut Paoli-Calmettes, Centre de Recherche en Cancérologie de Marseille, Aix-Marseille University, Marseille, France.
Lenaïg MescamDepartment of Pathology, Institut Paoli-Calmettes, Centre de Recherche en Cancérologie de Marseille, Aix-Marseille University, Marseille, France.
Lukas PlankDepartment of Pathological Anatomy, University Hospital Martin, Jessenius Faculty of Medicine, Comenius University, Martin, Slovakia.
Lise Mette Rahbek GjerdrumDepartment of Pathology, Copenhagen University Hospital-Zealand University Hospital, Roskilde, Denmark.
Nicolas Lopez-HisijosDepartment of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, TN, USA.
Timothy GreinerDepartment of Pathology, Microbiology, and Immunology, University of Nebraska Medical Center, Omaha, NE, USA.
Joseph KhouryDepartment of Pathology, Microbiology, and Immunology, University of Nebraska Medical Center, Omaha, NE, USA.
Wolfram KlapperSektion Hämatopathologie und Lymphknotenregister, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Ilske OschliesSektion Hämatopathologie und Lymphknotenregister, Universitätsklinikum Schleswig-Holstein, Campus Kiel, Kiel, Germany.
Andreas RosenwaldInstitute of Pathology, University of Würzburg, Würzburg, Germany.
German OttDepartment of Clinical Pathology, Robert-Bosch-Krankenhaus, and Dr. Margarete Fischer-Bosch Institute for Clinical Pharmacology, Stuttgart, Germany.
Ming-Qing DuDepartment of Pathology, University of Cambridge, Cambridge, UK.ORCID https://orcid.org/0000-0002-1017-5045

Funding

Biotechnology and Biological Sciences Research Council BBSRC BB/M011194/1Blood Cancer UK 19010Blood Cancer UK 19011Blood Cancer UK 22011Blood Cancer UK 24011Cancer Research UK C8333/A29707Cancer Research UK CRCBPA-Nov23/100001Deutsche Forschungsgemeinschaft KFO 5010/1
6 · The paper itself

Abstract

Terminal deoxynucleotidyl transferase (TdT) is occasionally expressed in large B-cell lymphoma (LBCL), and this causes difficulty in differential diagnosis from B-lymphoblastic leukaemia/lymphoma (B-ALL/LBL). We reviewed 31 cases of TdT-positive LBCL and B-ALL/LBL, and their final diagnosis included 19 diffuse large/high-grade BCLs with MYC and BCL2 rearrangements (five DLBCL-MYC/BCL2, 14 HGBCL-MYC/BCL2), three DLBCL not otherwise specified (NOS), three HGBCL-NOS, four B-ALL/LBL, and two unclassifiable cases. TdT was variably expressed in all these cases, without any clear demarcation among different groups. Loss or partial loss of CD20 expression was seen in 13/17 DLBCL/HGBCL-MYC/BCL2, 2/3 HGBCL-NOS, and 2/2 unclassified, albeit not in DLBCL-NOS. Expression of BCL6 and/or MUM1 was seen in 3/4 B-ALL/LBLs and 2/2 unclassified. Next-generation sequencing revealed characteristic mutations associated with follicular lymphoma and its high-grade transformation in each DLBCL/HGBCL-MYC/BCL2, and also frequent variants in genes targeted by somatic hypermutation (SHM) in almost all DLBCL/HGBCL-MYC/BCL2, DLBCL-NOS, and HGBCL-NOS but one case. In contrast, such mutations were absent in B-ALL/LBL. There were no pathognomonic mutations in the two unclassifiable cases, although one showed a moderate level of somatic mutations in its rearranged IGHV. Furthermore, in three cases of TdT-positive HGBCL-MYC/BCL2, studies of previous or concurrent follicular lymphoma demonstrated their divergent evolution from an IGH::BCL2-positive cell population following acquisition of MYC translocation. In conclusion, mutation profiling analysis including the SHM target genes is highly valuable in the differential diagnosis between TdT-positive LBCL and B-ALL/LBL. © 2025 The Author(s). The Journal of Pathology published by John Wiley & Sons Ltd on behalf of The Pathological Society of Great Britain and Ireland.

Indexed as

Biomarkers, TumorDNA NucleotidylexotransferaseLymphoma, Large B-Cell, DiffuseMutationPrecursor Cell Lymphoblastic Leukemia-LymphomaAdolescentAdultAgedAged, 80 and overDiagnosis, DifferentialDNA Mutational AnalysisFemaleHumansMaleMiddle AgedProto-Oncogene Proteins c-bcl-2BCL2 protein, humanBiomarkers, TumorDNA NucleotidylexotransferaseProto-Oncogene Proteins c-bcl-2Proto-Oncogene Proteins c-mycB‐lymphoblastic leukaemia/lymphomadifferential diagnosishigh‐grade B‐cell lymphomasomatic hypermutationTdT expression

Identifiers

PMID41047873
PMCPMC12596909

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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.