Evidence map›Paper›PMID 26101854›Full record

ArticleOncotarget2015

Age cutoff for Epstein-Barr virus-positive diffuse large B-cell lymphoma--is it necessary?

Chi Young Ok, Qing Ye, Ling Li, Ganiraju C Manyam, Lijuan Deng, Rashmi R Goswami, Xiaoxiao Wang, Santiago Montes-Moreno, Carlo Visco, Alexandar Tzankov and 24 more

Open access · diamondAbstract read
In one paragraph

Article in Oncotarget, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  3. Programmed cell death-ligand 1 (PD-L1)Clinical and experimental medicine · 2022
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  12. Review
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  14. Prognostic and biological significance of survivin expression in patients with diffuse large B-cell lymphoma treated with rituximab-CHOP therapy.Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc · 2015
    Article
  15. 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

34 authors at 20 institutions in 8 countries.

Chi Young OkDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Qing YeDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Ling LiDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Ganiraju C ManyamDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Lijuan DengDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Rashmi R GoswamiDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Xiaoxiao WangDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Santiago Montes-MorenoHospital Universitario Marques de Valdecilla, Santander, Spain.
Carlo ViscoSan Bortolo Hospital, Vicenza, Italy.
Alexandar TzankovUniversity Hospital, Basel, Switzerland.
Karen DybkaerAalborg University Hospital, Aalborg, Denmark.
Li ZhangDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Jeremy AbramsonMassachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
Aliyah R SohaniMassachusetts General Hospital and Harvard Medical School, Boston, Massachusetts, USA.
April ChiuMemorial Sloan-Kettering Cancer Center, New York, New York, USA.
Attilio OraziWeill Medical College of Cornell University, New York, New York, USA.
Youli ZuHouston Methodist Hospital, Houston, Texas, USA.
Govind BhagatColumbia University Medical Center and New York Presbyterian Hospital, New York, New York, USA.
Kristy L RichardsUniversity of North Carolina School of Medicine, Chapel Hill, North Carolina, USA.
Eric D HsiCleveland Clinic, Cleveland, Ohio, USA.
William W L ChoiUniversity of Hong Kong, Li Ka Shing Faculty of Medicine, Hong Kong, China.
J Han van KriekenRadboud University, Nijmegen Medical Centre, Nijmegen, the Netherlands.
Jooryung HuhAsan Medical Center, Ulsan University College of Medicine, Seoul, Korea.
Maurilio PonzoniSan Raffaele H. Scientific Institute, Milan, Italy.
Andrés J M FerreriSan Raffaele H. Scientific Institute, Milan, Italy.
Shanxiang ZhangIndiana University School of Medicine, Indianapolis, Indiana, USA.
Ben M ParsonsGundersen Lutheran Health System, La Crosse, Wisconsin, USA.
Mina XuYale University School of Medicine, New Haven, Connecticut, USA.
Michael B MøllerOdense University Hospital, Odense, Denmark.
Jane N WinterFeinberg School of Medicine, Northwestern University, Chicago, Illinois, USA.
Miguel A PirisHospital Universitario Marques de Valdecilla, Santander, Spain.
Zijun Y Xu-MonetteDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
L Jeffrey MedeirosDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
Ken H YoungDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
The University of Texas MD Anderson Cancer Center · USHarvard University · USMarqués de Valdecilla University Hospital · ESSan Raffaele University of Rome · ITAalborg University Hospital · DKAsan Medical Center · KRCleveland Clinic · USCornell University · USGundersen Health System · USIndiana University School of MedicineMemorial Sloan Kettering Cancer Center · USMethodist Hospital · USNewYork–Presbyterian Hospital · USNorthwestern University · USOdense University Hospital · DKOspedale San Bortolo · ITRadboud University Nijmegen · NLUniversity Hospital of Basel · CHUniversity of Hong Kong · HKUniversity of North Carolina at Chapel Hill · US

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Tumor Environment and Metastasis (TEAM) Research ProgramP30CA060553 · NCI · NORTHWESTERN UNIVERSITY AT CHICAGO · PI Daniela E Matei · 1993 to 2026
$153.9M
P4 -TARGETING MULTIPLE MYELOMA BY COMBINING CDK INHIBITORS AND BCL-2 ANTAGONISTSP50CA142509 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2010 to 2014
$11.1M
Convergence of MicroRNAs and p53 Signaling in Multiple Myeloma: Environmental CoR01CA138688 · NCI · UNIVERSITY OF LOUISVILLE · PI LI, YONG · 2009 to 2017
$2.9M
MYC as a Biomarker in Aggressive Non-Hodgkin LymphomaR01CA187415 · NCI · CLEVELAND CLINIC LERNER COM-CWRU · PI LI, YONG · 2015 to 2019
$2.2M
UT M.D. Anderson Cancer Center Lymphoma SPOREP50CA136411 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI KWAK, LARRY W · 2009 to 2011
$1.5M
NCI NIH HHS CA016672NCI NIH HHS P30 CA016672NCI NIH HHS P30 CA060553NCI NIH HHS P50 CA136411NCI NIH HHS P50CA136411NCI NIH HHS P50 CA142509NCI NIH HHS P50CA142509NCI NIH HHS R01 CA138688NCI NIH HHS R01CA138688NCI NIH HHS R01 CA187415NCI NIH HHS R01CA187415
6 · The paper itself

Abstract

Epstein-Barr virus-positive diffuse large B-cell lymphoma of the elderly (EBV+ DLBCL-e) is a molecularly distinct variant of DLBCL, characterized by a monoclonal B-cell proliferation that occurs in patients >50 years of age without a history or clinicopathologic evidence of immunodeficiency. However, patients with EBV+ DLBCL younger than 50-years-old also exist in Western countries. We evaluated the clinicopathologic, immunophenotypic and genetic features in Cacausian patients with EBV+ DLBCL who are ≤50 years of age and compared this patient group to patients who are >50 years. In patients who are ≤50 years, less frequent expression of BCL6 and a trend of more frequent expression of CD30 and pSTAT3 were found in patients with EBV+ DLBCL. In patients who are >50 years, common expression of CD30, p50, pSTAT3 and less frequent expression of BCL6 were observed. Older patients also more commonly had a poor performance status (ECOG≥2). Comparing EBV+ DLBCL patients in ≤50 years versus >50 years, both groups had similar clinicopathologic, immunophenotypic and genetic features. Gene expression profiling, microRNA profiling and treatment outcome of the younger patients with EBV+ DLBCL was not distinctive from tumors in older patients. Based on our data, we suggest that the arbitrary age cutoff for EBV+ DLBCL is unnecessary and should be eliminated in the WHO lymphoma classification scheme.

Indexed as

AdolescentAdultAgedAged, 80 and overAge FactorsAnimalsBiomarkers, TumorEpstein-Barr Virus InfectionsFemaleGene Expression ProfilingHumansImmunohistochemistryImmunophenotypingIn Situ HybridizationLymphoma, Large B-Cell, DiffuseMaleBiomarkers, TumorDLBCLEBVelderlygene expression profiling

Identifiers

PMID26101854
PMCPMC4546442
OpenAlexW2127498248

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Registered trials

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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.