Evidence map›Paper›PMID 25452615›Full record

Trial reportBlood2015

BCL2 mutations are associated with increased risk of transformation and shortened survival in follicular lymphoma.

Cristina Correia, Paula A Schneider, Haiming Dai, Ahmet Dogan, Matthew J Maurer, Amy K Church, Anne J Novak, Andrew L Feldman, Xiaosheng Wu, Husheng Ding and 12 more

Open access · bronzeAbstract readClinical Trial
In one paragraph

Trial report in Blood, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 1 pooled it
8.9field-weighted citation impact, top 1% 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

78 citing papers in PubMed, 1 synthesis or guideline pooled it, 135 citations in OpenAlex.

  1. Pooled it
  2. Exploratory biomarker analysis from a phase III study of the PI3K inhibitor, copanlisib, in combination with rituximab in patients with indolent non-Hodgkin lymphoma, a retrospective study.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2025
    Trial
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  7. 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
  8. Review
  9. Article
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  11. Article
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  13. Article
  14. PAQR4 oncogene: a novel target for cancer therapy.Medical oncology (Northwood, London, England) · 2024
    Review
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  18. Identification of closely related species inFrontiers in microbiology · 2024
    Article
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  20. Article

18 more citing papers are in PubMed but not listed here.

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

22 authors at 3 institutions in 2 countries.

Cristina CorreiaDivision of Oncology Research, Department of Oncology.
Paula A SchneiderDivision of Oncology Research, Department of Oncology.
Haiming DaiDivision of Oncology Research, Department of Oncology.
Ahmet DoganDivision of Hematopathology, Department of Laboratory Medicine and Pathology.
Matthew J MaurerDivision of Biomedical Statistics and Bioinformatics, Department of Health Sciences Research.
Amy K ChurchDivision of Hematology, Department of Medicine.
Anne J NovakDivision of Hematology, Department of Medicine.
Andrew L FeldmanDivision of Hematopathology, Department of Laboratory Medicine and Pathology.
Xiaosheng WuDepartment of Immunology, and.
Husheng DingDivision of Oncology Research, Department of Oncology.
X Wei MengDivision of Oncology Research, Department of Oncology.
James R CerhanDivision of Epidemiology, Department of Health Sciences Research, Mayo Clinic, Rochester, MN; and.
Susan L SlagerDivision of Biomedical Statistics and Bioinformatics, Department of Health Sciences Research.
William R MaconDivision of Hematopathology, Department of Laboratory Medicine and Pathology.
Thomas M HabermannDivision of Hematology, Department of Medicine.
Judith E KarpDivision of Hematological Malignancies, Sidney Kimmel Cancer Center at Johns Hopkins, Baltimore, MD.
Steven D GoreDivision of Hematological Malignancies, Sidney Kimmel Cancer Center at Johns Hopkins, Baltimore, MD.
Neil E KayDivision of Hematology, Department of Medicine.
Diane F JelinekDivision of Hematology, Department of Medicine, Department of Immunology, and.
Thomas E WitzigDivision of Hematology, Department of Medicine.
Grzegorz S NowakowskiDivision of Hematology, Department of Medicine.
Scott H KaufmannDivision of Oncology Research, Department of Oncology, Division of Hematology, Department of Medicine.
Department of Medical Sciences · BYSidney Kimmel Cancer Center · USMayo Clinic in Florida · US

Funding

Women's Cancer ProgramP30CA015083 · NCI · MAYO CLINIC ROCHESTER · PI Felicity Enders · 1985 to 2026
$151.3M
The Role of Monocytes in non-Hodgkin LymphomaP50CA097274 · NCI · UNIVERSITY OF IOWA · PI WEINER, GEORGE J. · 2002 to 2021
$45.7M
Combination Therapy in B-Chronic Lymphocytic LeukemiaR01CA095241 · NCI · MAYO CLINIC ROCHESTER · PI KAY, NEIL E · 2002 to 2012
$5.7M
Targeting Epigenomics in Myeloid NeoplasmsK24CA111717 · NCI · YALE UNIVERSITY · PI GORE, STEVEN D · 2005 to 2015
$1.7M
Anticancer drug-induced BH3-only protein.Bak interactionsR01CA166741 · NCI · MAYO CLINIC ROCHESTER · PI KAUFMANN, SCOTT H · 2012 to 2016
$1.6M
NCI NIH HHS K24 CA111717NCI NIH HHS P30 CA015083NCI NIH HHS P50 CA097274NCI NIH HHS R01 CA095241NCI NIH HHS R01 CA166741NCI NIH HHS R01 CA95241
6 · The paper itself

Abstract

Follicular lymphoma (FL), an indolent neoplasm caused by a t(14;18) chromosomal translocation that juxtaposes the BCL2 gene and immunoglobulin locus, has a variable clinical course and frequently undergoes transformation to an aggressive lymphoma. Although BCL2 mutations have been previously described, their relationship to FL progression remains unclear. In this study, we evaluated the frequency and nature of BCL2 mutations in 2 independent cohorts of grade 1 and 2 FLs, along with the correlation between BCL2 mutations, transformation risk, and survival. The prevalence of BCL2 coding sequence mutations was 12% in FL at diagnosis and 53% at transformation (P < .0001). The presence of these BCL2 mutations at diagnosis correlated with an increased risk of transformation (hazard ratio 3.6; 95% CI, 2.0-6.2; P < .0001) and increased risk of death due to lymphoma (median survival of 9.5 years with BCL2 mutations vs 20.4 years without; P = .012). In a multivariate analysis, BCL2 mutations and high FL international prognostic index were independent risk factors for transformation and death due to lymphoma. Some mutant Bcl-2 proteins exhibited enhanced antiapoptotic capacity in vitro. Accordingly, BCL2 mutations can affect antiapoptotic Bcl-2 function, are associated with increased activation-induced cytidine deaminase expression, and correlate with increased risk of transformation and death due to lymphoma.

Indexed as

MutationAdultAgedAged, 80 and overAge FactorsCell Transformation, NeoplasticChromosomes, Human, Pair 14Chromosomes, Human, Pair 18Cohort StudiesCytidine DeaminaseDisease-Free SurvivalFemaleGene Expression Regulation, EnzymologicGene Expression Regulation, NeoplasticHumansImmunoglobulinsCytidine DeaminaseImmunoglobulinsProto-Oncogene Proteins c-bcl-2

Identifiers

PMID25452615
PMCPMC4304111
OpenAlexW1973686119

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.