Evidence map›Paper›PMID 28745330›Full record

ArticleLeukemia2018

Concordant bone marrow involvement of diffuse large B-cell lymphoma represents a distinct clinical and biological entity in the era of immunotherapy.

Z Yao, L Deng, Z Y Xu-Monette, G C Manyam, P Jain, A Tzankov, C Visco, G Bhagat, J Wang, K Dybkaer and 17 more

Open access · bronzeAbstract read
In one paragraph

Article in Leukemia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
4.1field-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

33 citing papers in PubMed, 56 citations in OpenAlex.

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  10. Lacrimal sac Diffuse Large B-Cell Lymphoma Presenting as Sudden-Onset Binocular Diplopia.European journal of case reports in internal medicine · 2024
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  15. A bone-based 3D scaffold as anFrontiers in oncology · 2022
    Article
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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

27 authors at 16 institutions in 7 countries.

Z YaoDepartment of Medical Oncology, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China.
L DengKey laboratory of Carcinogenesis and Translational Research (Ministry of Education), Department of Lymphoma, Peking University Cancer Hospital & Institute, Beijing, China.
Z Y Xu-MonetteDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
G C ManyamDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
P JainDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
A TzankovUniversity of Basel, Hospital, Basel, Switzerland.
C ViscoSan Bortolo Hospital, Vicenza, Italy.
G BhagatColumbia University Medical Center and New York Presbyterian Hospital, New York, NY, USA.
J WangDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
K DybkaerAalborg University Hospital, Aalborg, Denmark.
W TamWeill Medical College of Cornell University, New York, NY, USA.
E D HsiCleveland Clinic, Cleveland, OH, USA.
J H van KriekenRadboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.
M PonzoniSan Raffaele H. Scientific Institute, Milan, Italy.
A J M FerreriSan Raffaele H. Scientific Institute, Milan, Italy.
M B MøllerOdense University Hospital, Odense, Denmark.
J N WinterFeinberg School of Medicine, Northwestern University, Chicago, IL, USA.
M A PirisHospital Universitario Marqués de Valdecilla, Santander, Spain.
L FayadDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Y LiuDepartment of Medical Oncology, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China.
Y SongDepartment of Medical Oncology, Affiliated Cancer Hospital of Zhengzhou University, Zhengzhou, China.
R Z OrlowskiDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
H KantarjianDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
L J MedeirosDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Y LiDepartment of Cancer Biology, Cleveland Clinic, Lerner Research Institute, Cleveland, OH, USA.
J CortesDepartment of Leukemia, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
K H YoungDepartment of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX, USA.
The University of Texas MD Anderson Cancer Center · USZhengzhou University · CNSan Raffaele University of Rome · ITAalborg University Hospital · DKCleveland Clinic · USCleveland Clinic Lerner College of Medicine · USCornell University · USMarqués de Valdecilla University Hospital · ESNewYork–Presbyterian Hospital · USNorthwestern University · USOdense University Hospital · DKOspedale San Bortolo · ITPeking University · CNRadboud University Nijmegen · NLThe University of Texas Health Science Center at Houston · USUniversity of Basel · CH

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Fabien Delerue · 1985 to 2026
$290.8M
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 YOUNES, ANAS · 2009 to 2011
$1.5M
Deep Sequencing of Small Regulatory RNAs in Diffuse Large B cell LymphomaRC1CA146299 · NCI · SCRIPPS RESEARCH INSTITUTE, THE · PI XIAO, CHANGCHUN · 2009 to 2010
$1000k
NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA136411NCI NIH HHS P50 CA142509NCI NIH HHS R01 CA138688NCI NIH HHS R01 CA187415NCI NIH HHS RC1 CA146299
6 · The paper itself

Abstract

In diffuse large B-cell lymphoma (DLBCL), the clinical and biological significance of concordant and discordant bone marrow (BM) involvement have not been well investigated. We evaluated 712 de novo DLBCL patients with front-line rituximab-containing treatment, including 263 patients with positive and 449 with negative BM status. Compared with negative BM disease, concordant BM adversely impacted overall and progression-free survival, independent of the International Prognostic Index (IPI) and cell-of-origin classification. Once BM is concordantly involved, poor prognosis was not associated with the extent of BM involvement. Conversely, patients with discordant BM showed favorable overall survival similar to stage I-II DLBCL. A BM-adjusted IPI, using three parameters: concordant BM involvement, age >60 years, and performance status >1, improves the risk stratification for DLBCL with positive BM. Intensive immunochemotherapy seemingly rendered survival benefit for patients with concordant BM, as did rituximab maintenance for the discordant BM group. Frequently revealing adverse clinical and molecular characteristics, patients with concordant BM demonstrated gene expression signatures relevant to tumor cell proliferation, migration and immune escape. In conclusion, clinical and biological heterogeneity is seen in DLBCL with positive BM but concordant BM involvement represents a distinct subset with unfavorable gene signatures, high-risk clinicopathologic features and poor prognosis.

Indexed as

AdolescentAdultAgedAged, 80 and overAntineoplastic Combined Chemotherapy ProtocolsBone MarrowDisease-Free SurvivalFemaleHumansImmunologic FactorsImmunotherapyLymphoma, Large B-Cell, DiffuseMaleMiddle AgedPrognosisYoung AdultImmunologic Factors

Identifiers

PMID28745330
PMCPMC5985660
OpenAlexW2735832977

What OpenQuestion holds

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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.