Evidence map›Paper›PMID 23255553›Full record

ArticleBlood2013

CCND2 rearrangements are the most frequent genetic events in cyclin D1(-) mantle cell lymphoma.

Itziar Salaverria, Cristina Royo, Alejandra Carvajal-Cuenca, Guillem Clot, Alba Navarro, Alejandra Valera, Joo Y Song, Renata Woroniecka, Grzegorz Rymkiewicz, Wolfram Klapper and 14 more

Abstract read
In one paragraph

Article in Blood, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 78 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
78citing papers in PubMed, 3 pooled it
8.7field-weighted citation impact, top 2% 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, 3 syntheses or guidelines pooled it, 207 citations in OpenAlex.

  1. [The guideline of the diagnosis and treatment of mantle cell lymphoma in China (2022)].Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi · 2022
    Guideline
  2. Pooled it
  3. Non-Hodgkin's lymphomas, version 4.2014.Journal of the National Comprehensive Cancer Network : JNCCN · 2014
    Guideline
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18 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

24 authors at 12 institutions in 6 countries.

Itziar SalaverriaDepartment of Pathology, Hematopathology Unit, Hospital Clínic, Institut d'Investigacions Biomèdiques August Pi i Sunyer, University of Barcelona, Barcelona, Spain.
Cristina Royo
Alejandra Carvajal-Cuenca
Guillem Clot
Alba Navarro
Alejandra Valera
Joo Y Song
Renata Woroniecka
Grzegorz Rymkiewicz
Wolfram Klapper
Elena M Hartmann
Pierre Sujobert
Iwona Wlodarska
Judith A Ferry
Philippe Gaulard
German Ott
Andreas Rosenwald
Armando Lopez-Guillermo
Leticia Quintanilla-Martinez
Nancy L Harris
Elaine S Jaffe
Reiner Siebert
Elias Campo
Sílvia Beà
Universitat de Barcelona · ESHôpitaux Universitaires Henri-Mondor · FRKiel University · DEMassachusetts General Hospital · USUniversity of Würzburg · DECenter for Cancer Research · USHospital Clínic de Barcelona · ESKU Leuven · BENational Cancer Institute · USRobert Bosch Hospital · DEThe Maria Sklodowska-Curie National Research Institute of Oncology · PLUniversity of Tübingen · DE

Funding

Lymphoma Disease Discovery and DefintionZIASC000550 · NCI · DIVISION OF CLINICAL SCIENCES - NCI · PI JAFFE, ELAINE · 2009 to 2025
$16.9M
Hematopathology DiagnosisZIABC011070 · NCI · DIVISION OF BASIC SCIENCES - NCI · PI JAFFE, ELAINE · 2009 to 2025
$14.5M
6 · The paper itself

Abstract

Cyclin D1(-) mantle cell lymphomas (MCLs) are not well characterized, in part because of the difficulties in their recognition. SOX11 has been identified recently as a reliable biomarker of MCL that is also expressed in the cyclin D1(-) variant. We investigated 40 lymphomas with MCL morphology and immunophenotype that were negative for cyclin D1 expression/t(11;14)(q13;q32) but positive for SOX11. These tumors presented clinically with generalized lymphadenopathy, advanced stage, and poor outcome (5-year overall survival, 48%). Chromosomal rearrangements of the CCND2 locus were detected in 55% of the cases, with an IG gene as partner in 18 of 22, in particular with light chains (10 IGK@ and 5 IGL@). No mutations in the phosphorylation motifs of CCND1, CCND2, or CCND3 were detected. The global genomic profile and the high complexity of the 32 cyclin D1(-) SOX11(+) MCL patients analyzed by copy number arrays were similar to the conventional cyclin D1/SOX11 MCL. 17p deletions and high Ki67 expression conferred a significantly worse outcome for the patients. This comprehensive characterization of a large series of cyclin D1(-) MCL patients indicates that these tumors are clinically and biologically similar to the conventional cyclin D1(+) MCL and provides a basis for the proper identification and clinical management of these patients.

Indexed as

AdultAgedAged, 80 and overCyclin D1Cyclin D2Cyclin D3DNA Copy Number VariationsDNA Mutational AnalysisFemaleGene RearrangementHumansImmunohistochemistryIn Situ Hybridization, FluorescenceLymphoma, Mantle-CellMaleMiddle AgedCCND1 protein, humanCCND2 protein, humanCCND3 protein, humanCyclin D1Cyclin D2Cyclin D3RNA, MessengerSOX11 protein, humanSOXC Transcription Factors

Identifiers

PMID23255553
PMCPMC3578954
OpenAlexW2072839232

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.