Evidence map›Paper›PMID 24625556›Full record

Trial reportPloS one2014

Deregulation of COMMD1 is associated with poor prognosis in diffuse large B-cell lymphoma.

Minna Taskinen, Riku Louhimo, Satu Koivula, Ping Chen, Ville Rantanen, Harald Holte, Jan Delabie, Marja-Liisa Karjalainen-Lindsberg, Magnus Björkholm, Øystein Fluge and 6 more

Registry-linked trialOpen access · goldAbstract readClinical Trial, Phase IIMulticenter Study
In one paragraph

Trial report in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01502982 (CHOEP-14 + Rituximab With CNS Prophylaxis in Patients Less Than 65 Years With Diffuse Large B-Cell Lymphoma/Follicular Lymphoma Grade III, Stage II-IV With Risk Factors), which is not on this map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.9field-weighted citation impact, top 16% 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.

NCT01502982 phase2completednot on this map

CHOEP-14 + Rituximab With CNS Prophylaxis in Patients Less Than 65 Years With Diffuse Large B-Cell Lymphoma/Follicular Lymphoma Grade III, Stage II-IV With Risk Factors (Age Adjusted IPI) ≥ 2. A Phase II Study

TypeinterventionalSponsorNordic Lymphoma GroupRan2004 to 2014Enrolled160ConditionsDiffuse Large B-Cell LymphomaArmsR-CHOEP14x6+HD-AraC+HD-Mtx
3 · Its place in the literature

Who cites it

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. COMMD3 Expression Affects Angiogenesis through the HIF1Oxidative medicine and cellular longevity · 2022
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
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

16 authors at 7 institutions in 4 countries.

Minna TaskinenDepartment of Oncology, Helsinki University Central Hospital, Helsinki, Finland; Genome Scale Biology Program, University of Helsinki, Helsinki, Finland.
Riku LouhimoGenome Scale Biology Program, University of Helsinki, Helsinki, Finland.
Satu KoivulaDepartment of Oncology, Helsinki University Central Hospital, Helsinki, Finland; Genome Scale Biology Program, University of Helsinki, Helsinki, Finland.
Ping ChenGenome Scale Biology Program, University of Helsinki, Helsinki, Finland.
Ville RantanenGenome Scale Biology Program, University of Helsinki, Helsinki, Finland.
Harald HolteDepartment of Oncology, Oslo University Hospital, Oslo, Norway.
Jan DelabieDepartment of Pathology, Oslo University Hospital, Oslo, Norway.
Marja-Liisa Karjalainen-LindsbergDepartment of Pathology, Haartman Institute, University of Helsinki, Helsinki, Finland.
Magnus BjörkholmDepartment of Medicine, Karolinska University Hospital, Stockholm, Sweden.
Øystein FlugeDepartment of Oncology and Medical Physics, Haukeland University Hospital, Bergen, Norway.
Lars Møller PedersenDepartment of Hematology, Odense University Hospital, Odense, Denmark.
Karin FjordénDepartment of Oncology, Lund University Hospital, Lund, Sweden.
Mats JerkemanDepartment of Oncology, Lund University Hospital, Lund, Sweden.
Mikael ErikssonDepartment of Oncology, Lund University Hospital, Lund, Sweden.
Sampsa HautaniemiGenome Scale Biology Program, University of Helsinki, Helsinki, Finland.
Sirpa LeppäDepartment of Oncology, Helsinki University Central Hospital, Helsinki, Finland; Genome Scale Biology Program, University of Helsinki, Helsinki, Finland.
University of Helsinki · FILund University · SEOslo University Hospital · NOHaukeland University Hospital · NOHelsinki University Hospital · FIKarolinska University Hospital · SEOdense University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite improved survival for the patients with diffuse large B-cell lymphoma (DLBCL), the prognosis after relapse is poor. The aim was to identify molecular events that contribute to relapse and treatment resistance in DLBCL.

methodsWe analysed 51 prospectively collected pretreatment tumour samples from clinically high risk patients treated in a Nordic phase II study with dose-dense chemoimmunotherapy and central nervous system prophylaxis with high resolution array comparative genomic hybridization (aCGH) and gene expression microarrays. Major finding was validated at the protein level immunohistochemically in a trial specific tissue microarray series of 70, and in an independent validation series of 146 patients.

resultsWe identified 31 genes whose expression changes were strongly associated with copy number aberrations. In addition, gains of chromosomes 2p15 and 18q12.2 were associated with unfavourable survival. The 2p15 aberration harboured COMMD1 gene, whose expression had a significant adverse prognostic impact on survival. Immunohistochemical analysis of COMMD1 expression in two series confirmed the association of COMMD1 expression with poor prognosis.

conclusionCOMMD1 is a potential novel prognostic factor in DLBCLs. The results highlight the value of integrated comprehensive analysis to identify prognostic markers and genetic driver events not previously implicated in DLBCL.

trial registrationClinicalTrials.gov NCT01502982.

Indexed as

Gene Expression Regulation, NeoplasticAdaptor Proteins, Signal TransducingAdultAgedCombined Modality TherapyComparative Genomic HybridizationFemaleGenetic Predisposition to DiseaseHumansImmunohistochemistryImmunotherapyLymphoma, Large B-Cell, DiffuseMaleMiddle AgedOligonucleotide Array Sequence AnalysisPrognosisAdaptor Proteins, Signal TransducingCOMMD1 protein, human

Identifiers

PMID24625556
PMCPMC3953211
OpenAlexW1997052954

What OpenQuestion holds

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Registered trials

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.