Evidence map›Paper›PMID 33811533›Full record

ArticleVirchows Archiv : an international journal of pathology2021

Lack of expression of LMO2 clone SP51 identifies MYC rearrangements in aggressive large B-cell lymphomas.

Ivonne Vazquez, Natalia Papaleo, Joan Lop, Anna Puiggros, Blanca Sanchez-Gonzalez, Ramon Diez-Feijoo, Eva Gimeno, Marcio Andrade-Campos, Antonio Salar, Blanca Espinet and 7 more

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Article in Virchows Archiv : an international journal of pathology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 35% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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  4. ChromogenicCancers · 2024
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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

17 authors at 4 institutions in 2 countries.

Ivonne VazquezDepartment of Pathology, Hospital del Mar, Institut Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0002-5305-1560
Natalia PapaleoDepartment of Pathology, Hospital del Mar, Institut Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.
Joan LopDepartment of Pathology, Hospital del Mar, Institut Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.
Anna PuiggrosDepartment of Pathology, Hospital del Mar, Institut Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0001-9627-4978
Blanca Sanchez-GonzalezDepartment of Hematology, Hospital del Mar, Institute Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.
Ramon Diez-FeijooDepartment of Hematology, Hospital del Mar, Institute Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.
Eva GimenoDepartment of Hematology, Hospital del Mar, Institute Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.
Marcio Andrade-CamposDepartment of Hematology, Hospital del Mar, Institute Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.
Antonio SalarDepartment of Hematology, Hospital del Mar, Institute Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0002-4652-4825
Blanca EspinetDepartment of Pathology, Hospital del Mar, Institut Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0002-4294-8145
Marta SalidoDepartment of Pathology, Hospital del Mar, Institut Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0001-9988-5977
Gustavo TapiaDepartment of Pathology, Hospital Germans Trias I Pujol, Institut Germans Trias I Pujol (IGTP), Badalona, Spain.ORCID https://orcid.org/0000-0003-1882-0368
Joaquim CarrerasDepartment of Pathology, School of Medicine, Tokai University, Isehara, Japan.
Ana FerrerDepartment of Pathology, Hospital del Mar, Institut Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0002-3381-9472
Leonor ArenillasDepartment of Pathology, Hospital del Mar, Institut Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0002-8176-7179
Xavier CalvoDepartment of Pathology, Hospital del Mar, Institut Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain.ORCID https://orcid.org/0000-0001-7934-9130
Luis ColomoDepartment of Pathology, Hospital del Mar, Institut Hospital del Mar d'Investigacions Mediques (IMIM), Barcelona, Spain. lcolomo@psmar.cat.ORCID http://orcid.org/0000-0001-5236-5085
Hospital del Mar Research Institute · ESUniversitat Pompeu Fabra · ESTokai University · JPUniversitat Autònoma de Barcelona · ES

Funding

Instituto de Salud Carlos III Fondo de Investigación Sanitaria (FIS) PI17/313
6 · The paper itself

Abstract

MYC rearrangements (MYC-R) confer unfavorable prognosis to large B-cell lymphomas (LBCL). Because of the low incidence of such genetic alteration, surrogates to screen MYC-R may be useful in daily practice. Previous studies suggested that clone 1A9-1 of LMO2 loss may be a good predictor for the presence of MYC-R in LBCL. The present study examines the utility of LMO2 clone SP51. For this purpose, we have analyzed 20 Burkitt lymphomas and 325 LBCL. Among them, 245 cases were studied prospectively using whole tissue sections, and 100 retrospectively by tissue microarrays. The cohort of CD10-positive prospective cases achieved the best results. Lack of LMO2 SP51 expression predicted the presence of MYC-R with high specificity, accuracy, positive and negative predictive value (PPV/NPV), and positive and negative likelihood ratios (PLR/NLR). Compared with MYC protein expression, LMO2 SP51 obtained significantly higher specificity, accuracy, PPV, and PLR (94%, 91%, 85%, and 14.33 vs 73%, 77%, 56%, and 3.26, respectively), and similar NPV and NLR (92% and 0.22 vs 95% and 0.12). Compared with LMO2 clone 1A9-1, the sensitivity of LMO2 SP51 was lower (79% vs 89%). We conclude that LMO2 SP51 may be a useful marker to screen MYC-R in CD10-positive LBCL.

Indexed as

Biomarkers, TumorGene RearrangementImmunohistochemistryAdaptor Proteins, Signal TransducingAdolescentAdultAgedAged, 80 and overChildChild, PreschoolFemaleHumansLIM Domain ProteinsLymphoma, Large B-Cell, DiffuseMaleMiddle AgedAdaptor Proteins, Signal TransducingBiomarkers, TumorLIM Domain ProteinsLMO2 protein, humanMYC protein, humanNeprilysinProto-Oncogene ProteinsProto-Oncogene Proteins c-mycImmunohistochemistryLarge B-cell lymphomaLMO2MYC

Identifiers

PMID33811533
OpenAlexW3139679832

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.