Evidence map›Paper›PMID 26910115›Full record

ArticleOncotarget2016

Stratifying diffuse large B-cell lymphoma patients treated with chemoimmunotherapy: GCB/non-GCB by immunohistochemistry is still a robust and feasible marker.

Ana Batlle-López, Sonia González de Villambrosía, Mazorra Francisco, Sefora Malatxeberria, Anabel Sáez, Carlos Montalban, Lydia Sánchez, Juan Garcia, Eva González-Barca, Andrés López-Hernández and 13 more

Open access · diamondAbstract readComparative Study
In one paragraph

Article in Oncotarget, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.2field-weighted citation impact, top 9% 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

14 citing papers in PubMed, 33 citations in OpenAlex.

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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

23 authors at 13 institutions in 4 countries.

Ana Batlle-LópezDepartments of Haematology and Pathology, Hospital Marques de Valdecilla, and IDIVAL, Santander, Spain.
Sonia González de VillambrosíaDepartments of Haematology and Pathology, Hospital Marques de Valdecilla, and IDIVAL, Santander, Spain.
Mazorra FranciscoDepartments of Haematology and Pathology, Hospital Marques de Valdecilla, and IDIVAL, Santander, Spain.
Sefora MalatxeberriaDepartments of Haematology and Pathology, Hospital Marques de Valdecilla, and IDIVAL, Santander, Spain.
Anabel SáezBiobanco del Sistema Sanitario Público de Andalucía, Granada, Spain.
Carlos MontalbanMD Anderson Cancer Center, Madrid, Spain.
Lydia SánchezBiotechnology Programme, Histology and Immunohistochemistry Core Unit, Spanish National Cancer Research Centre (CNIO), Madrid, Spain.
Juan GarciaPathology, MD Anderson Cancer Center, Madrid, Spain.
Eva González-BarcaDepartment of Haematology, Hospital de Bellvitge (ICOIRO), Barcelona, Spain.
Andrés López-HernándezDepartments of Pathology and Haematology, Hospital Vall d'Hebron, Barcelona, Spain.
M C Ruiz-MarcellanDepartments of Pathology and Haematology, Hospital Vall d'Hebron, Barcelona, Spain.
Manuela MollejoHospital Virgen de la Salud, Toledo, Spain.
Carlos GrandeHematology, Hospital 12 de Octubre, Madrid, Spain.
Kristy L RichardsDepartment of Hematology-Oncology, University of North Carolina School of Medicine, Chapel Hill, NC, USA.
Eric D HsiDepartment of Clinical Pathology, Cleveland Clinic, Cleveland, OH, USA.
Alexandar TzankovUniversity Hospital, Basel, Switzerland.
Carlo ViscoDepartment of Hematology, San Bortolo Hospital, Vicenza, Italy.
Zijun Y Xu-MonetteDepartment of Hematopathology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Xin CaoDepartment of Hematopathology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Ken H YoungDepartment of Hematopathology, University of Texas MD Anderson Cancer Center, Houston, TX, USA.
Miguel Ángel PirisDepartments of Haematology and Pathology, Hospital Marques de Valdecilla, and IDIVAL, Santander, Spain.
Eulogio CondeDepartments of Haematology and Pathology, Hospital Marques de Valdecilla, and IDIVAL, Santander, Spain.
Santiago Montes-MorenoDepartments of Haematology and Pathology, Hospital Marques de Valdecilla, and IDIVAL, Santander, Spain.
Instituto de Investigación Marqués de Valdecilla · ESThe University of Texas MD Anderson Cancer Center · USMD Anderson Cancer Center Madrid · ESVall d'Hebron Hospital Universitari · ESBellvitge University Hospital · ESBiobanco del Sistema Sanitario Público de Andalucía · ESCleveland Clinic · USHospital Virgen de la Salud · ESOspedale San Bortolo · ITResearch Institute Hospital 12 de Octubre · ESSpanish National Cancer Research Centre · ESUniversity Hospital of Basel · CHUniversity of North Carolina at Chapel Hill · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Diffuse large B cell lymphoma (DLBCL) is a heterogeneous group of aggressive lymphomas that can be classified into three molecular subtypes by gene expression profiling (GEP): GCB, ABC and unclassified. Immunohistochemistry-based cell of origin (COO) classification, as a surrogate for GEP, using three available immunohistochemical algorithms was evaluated in TMA-arranged tissue samples from 297 patients with de novo DLBCL treated by chemoimmunotherapy (R-CHOP and R-CHOP-like regimens). Additionally, the prognostic impacts of MYC, BCL2, IRF4 and BCL6 abnormalities detected by FISH, the relationship between the immunohistochemical COO classification and the immunohistochemical expression of MYC, BCL2 and pSTAT3 proteins and clinical data were evaluated. In our series, non-GCB DLBCL patients had significantly worse progression-free survival (PFS) and overall survival (OS), as calculated using the Choi, Visco-Young and Hans algorithms, indicating that any of these algorithms would be appropriate for identifying patients who require alternative therapies to R-CHOP. Whilst MYC abnormalities had no impact on clinical outcome in the non-GCB subtype, those patients with isolated MYC rearrangements and a GCB-DLBCL phenotype had worse PFS and therefore might benefit from novel treatment approaches.

Indexed as

AlgorithmsAntibodies, Monoclonal, Murine-DerivedAntineoplastic Combined Chemotherapy ProtocolsCohort StudiesCyclophosphamideDisease-Free SurvivalDoxorubicinHumansImmunohistochemistryLymphoma, Large B-Cell, DiffuseMiddle AgedPrednisoneRetrospective StudiesRituximabSurvival AnalysisVincristineAntibodies, Monoclonal, Murine-DerivedCyclophosphamideDoxorubicinPrednisoneR-CHOP protocolRituximabVincristineBCL2BCL6DLBCLMYCnon-GCB and GCB

Identifiers

PMID26910115
PMCPMC4951269
OpenAlexW2284991592

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.