Evidence map›Paper›PMID 32961552›Full record

ArticleBlood2021

Mutational landscape of gray zone lymphoma.

Clémentine Sarkozy, Stacy S Hung, Elizabeth A Chavez, Gerben Duns, Katsuyoshi Takata, Lauren C Chong, Tomohiro Aoki, Aixiang Jiang, Tomoko Miyata-Takata, Adèle Telenius and 14 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Blood, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
8.4field-weighted citation impact, top 2% of its field
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

55 citing papers in PubMed, 105 citations in OpenAlex.

  1. Article
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  3. Review
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  8. Review
  9. Article
  10. Article
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  12. Pediatric lymphomas: overview and diagnostic challenges.Virchows Archiv : an international journal of pathology · 2025
    Review
  13. Article
  14. Article
  15. Article
  16. Role of LMO7 in cancer (Review).Oncology reports · 2024
    Review
  17. Article
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  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 5 institutions in 3 countries.

Clémentine SarkozyCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Stacy S HungCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Elizabeth A ChavezCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Gerben DunsCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Katsuyoshi TakataCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Lauren C ChongCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Tomohiro AokiCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Aixiang JiangCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Tomoko Miyata-TakataCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Adèle TeleniusCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Graham W SlackCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Thierry Jo MolinaPathology Department, Necker Enfants Malades Hospital, Université Paris Descartes, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Susana Ben-NeriahCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Pedro FarinhaCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Peggy DartiguesPathology Department, Gustave Roussy, Université Paris-Saclay, INSERM U1170, Villejuif, France.
Diane DamottePathology Department, Groupe Hospitalier Cochin, AP-HP, Paris, France.
Anja MottokInstitute of Human Genetics, Ulm University and Ulm University Medical Center, Ulm, Germany.
Gilles A SallesINSERM Unité Mixte de Recherche (UMR) S1052, Centre National de la Recherche UMR 5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Rene-Olivier CasasnovasDepartment of Hematology, François Mitterrand University Hospital, INSERM U1231, Dijon, France.
Kerry J SavageCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Camille LaurentInstitut Universitaire du Cancer-Oncopole de Toulouse, CHU Toulouse, INSERM U1037, Centre de Recherche en Cancerologie de Toulouse-Purpan, Toulouse-Purpan, France; and.
David W ScottCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Alexandra Traverse-GlehenINSERM Unité Mixte de Recherche (UMR) S1052, Centre National de la Recherche UMR 5286, Centre de Recherche en Cancérologie de Lyon, Lyon, France.
Christian SteidlCentre for Lymphoid Cancer, British Columbia Cancer, Vancouver, BC, Canada.
Spinal Cord Injury BC · CAInserm · FRDélégation Paris 5 · FRHôpital Necker-Enfants Malades · FRUniversität Ulm · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The mutational landscape of gray zone lymphoma (GZL) has not yet been established, and differences from related entities are largely unknown. Here, we studied coding sequence mutations of 50 Epstein-Barr virus (EBV)-negative GZLs and 20 polymorphic EBV+ diffuse large B-cell lymphoma (DLBCL) not otherwise specified (poly-EBV-L) in comparison with classical Hodgkin lymphoma (cHL), primary mediastinal large B-cell lymphoma (PMBCL), and DLBCL. Exomes of 21 GZL and 7 poly-EBV-L cases, along with paired constitutional DNA, were analyzed as a discovery cohort, followed by targeted sequencing of 217 genes in an extension cohort of 29 GZL and 13 poly-EBV-L cases. GZL cases with thymic niche involvement (anterior mediastinal mass) exhibited a mutation profile closely resembling cHL and PMBCL, with SOCS1 (45%), B2M (45%), TNFAIP3 (35%), GNA13 (35%), LRRN3 (32%), and NFKBIA (29%) being the most recurrently mutated genes. In contrast, GZL cases without thymic niche involvement (n = 18) had a significantly distinct pattern that was enriched in mutations related to apoptosis defects (TP53 [39%], BCL2 [28%], BIRC6 [22%]) and depleted in GNA13, XPO1, or NF-κB signaling pathway mutations (TNFAIP3, NFKBIE, IKBKB, NFKBIA). They also exhibited more BCL2/BCL6 rearrangements compared with thymic GZL. Poly-EBV-L cases presented a distinct mutational profile, including STAT3 mutations and a significantly lower coding mutation load in comparison with EBV- GZL. Our study highlights characteristic mutational patterns in GZL associated with presentation in the thymic niche, suggesting a common cell of origin and disease evolution overlapping with related anterior mediastinal lymphomas.

Indexed as

MutationAdolescentAdultAgedAged, 80 and overEpstein-Barr Virus InfectionsFemaleHodgkin DiseaseHumansLymphoma, Large B-Cell, DiffuseMaleMediastinal NeoplasmsMiddle AgedThymus GlandYoung Adult

Identifiers

PMID32961552
OpenAlexW3149092134

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.