Evidence map›Paper›PMID 26307535›Full record

ArticleBlood2015

Cell of origin of transformed follicular lymphoma.

Robert Kridel, Anja Mottok, Pedro Farinha, Susana Ben-Neriah, Daisuke Ennishi, Yvonne Zheng, Elizabeth A Chavez, Hennady P Shulha, King Tan, Fong Chun Chan and 10 more

Open access · bronzeAbstract read
In one paragraph

Article in Blood, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed, 2 pooled it
8.6field-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

56 citing papers in PubMed, 2 syntheses or guidelines pooled it, 116 citations in OpenAlex.

  1. Pooled it
  2. [Chinese guidelines for diagnosis and treatment of follicular lymphoma(2023)].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2023
    Guideline
  3. Article
  4. Heterogeneity in primary gastrointestinal DLBCL: from clinical management to molecular mechanisms and treatment strategies.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2026
    Review
  5. Article
  6. Article
  7. Article
  8. Ocular adnexa follicular lymphoma: clinicopathological study of 23 patients.Virchows Archiv : an international journal of pathology · 2026
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Review
  20. Article
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

20 authors at 3 institutions in 2 countries.

Robert KridelCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada; Department of Pathology and Laboratory Medicine, and.
Anja MottokCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada; Department of Pathology and Laboratory Medicine, and.
Pedro FarinhaCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada; Department of Pathology and Laboratory Medicine, and.
Susana Ben-NeriahCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
Daisuke EnnishiCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
Yvonne ZhengCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
Elizabeth A ChavezCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
Hennady P ShulhaCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
King TanCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
Fong Chun ChanCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
Merrill BoyleCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
Barbara MeissnerCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
Adele TeleniusCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada;
Laurie H SehnCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada; Department of Medicine, University of British Columbia, Vancouver, BC, Canada;
Marco A MarraCanada's Michael Smith Genome Sciences Centre, BC Cancer Agency, Vancouver, BC, Canada; Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada; and.
Sohrab P ShahDepartment of Pathology and Laboratory Medicine, and Molecular Oncology, BC Cancer Agency, Vancouver, BC, Canada.
Christian SteidlCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada; Department of Pathology and Laboratory Medicine, and.
Joseph M ConnorsCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada; Department of Medicine, University of British Columbia, Vancouver, BC, Canada;
David W ScottCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada; Department of Medicine, University of British Columbia, Vancouver, BC, Canada;
Randy D GascoyneCentre for Lymphoid Cancer, BC Cancer Agency, Vancouver, BC, Canada; Department of Pathology and Laboratory Medicine, and.
BC Cancer Agency · CAEmory University Hospital · USUniversity of British Columbia · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Follicular lymphoma (FL) is an indolent disease but transforms in 2% to 3% of patients per year into aggressive, large cell lymphoma, a critical event in the course of the disease associated with increased lymphoma-related mortality. Early transformation cannot be accurately predicted at the time of FL diagnosis and the biology of transformed FL (TFL) is poorly understood. Here, we assembled a cohort of 126 diagnostic FL specimens including 40 patients experiencing transformation (<5 years) and 86 patients not experiencing transformation for at least 5 years. In addition, we assembled an overlapping cohort of 155 TFL patients, including 114 cases for which paired samples were available, and assessed temporal changes of routinely available biomarkers, outcome after transformation, as well as molecular subtypes of TFL. We report that the expression of IRF4 is an independent predictor of early transformation (Hazard ratio, 13.3; P < .001). We also show that composite histology at the time of transformation predicts favorable prognosis. Moreover, applying the Lymph2Cx digital gene expression assay for diffuse large B-cell lymphoma (DLBCL) cell-of-origin determination to 110 patients with DLBCL-like TFL, we demonstrate that TFL is of the germinal-center B-cell-like subtype in the majority of cases (80%) but that a significant proportion of cases is of the activated B-cell-like (ABC) subtype (16%). These latter cases are commonly negative for BCL2 translocation and arise preferentially from BCL2 translocation-negative and/or IRF4-expressing FLs. Our study demonstrates the existence of molecular heterogeneity in TFL as well as its relationship to the antecedent FL.

Indexed as

B-LymphocytesCARD Signaling Adaptor ProteinsCD79 AntigensCell Transformation, NeoplasticFemaleGerminal CenterGuanylate CyclaseHumansLymphoma, FollicularMaleMiddle AgedMutationMyeloid Differentiation Factor 88Proto-Oncogene Proteins c-bcl-2BCL2 protein, humanCARD11 protein, humanCARD Signaling Adaptor ProteinsCD79 AntigensCD79B protein, humanGuanylate CyclaseMYD88 protein, humanMyeloid Differentiation Factor 88Proto-Oncogene Proteins c-bcl-2

Identifiers

PMID26307535
PMCPMC4626253
OpenAlexW1836083640

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.