Evidence map›Paper›PMID 23023716›Full record

ReviewThe Journal of clinical investigation2012

New molecular insights into peripheral T cell lymphomas.

Stefano A Pileri, Pier Paolo Piccaluga

Abstract readReview
In one paragraph

Review in The Journal of clinical investigation, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
–field-weighted citation impact
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

22 citing papers in PubMed.

  1. Trial
  2. Review
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  10. Review
  11. Article
  12. Article
  13. Comprehensive serum cytokine analysis identifies IL-1RA and soluble IL-2Rα as predictors of event-free survival in T-cell lymphoma.Annals of oncology : official journal of the European Society for Medical Oncology · 2016
    Article
  14. SNPs Array Karyotyping in Non-Hodgkin Lymphoma.Microarrays (Basel, Switzerland) · 2015
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Molecular genetics of peripheral T-cell lymphomas.International journal of hematology · 2014
    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

2 authors.

Stefano A PileriHematopathology Section, Department of Hematology and Oncology L. and A. Seràgnoli, S. Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy. stefano.pileri@unibo.it
Pier Paolo Piccaluga

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral T cell lymphomas (PTCLs) are heterogeneous neoplasms and represent about 12% of all lymphoid malignancies. They are often regarded as "orphan diseases," a designation that does not reflect their real incidence but rather signifies the difficulties encountered in their classification, diagnosis, and treatment. Here we revise the current understanding of the pathobiological characteristics of the most common nodal PTCLs by focusing on the contribution given by high-throughput technologies and the identification of potential therapeutic targets proposed by translational studies.

Indexed as

Angiogenesis InhibitorsAntibodies, MonoclonalAntigens, NeoplasmAntigens, SurfaceGene Expression ProfilingGene Expression Regulation, NeoplasticHistone Deacetylase InhibitorsHumansLymphoma, T-Cell, PeripheralMicroRNAsMolecular Targeted TherapyNeoplasm ProteinsNeoplastic Stem CellsPlatelet-Derived Growth FactorPrognosisProtein Kinase InhibitorsAngiogenesis InhibitorsAntibodies, MonoclonalAntigens, NeoplasmAntigens, SurfaceHistone Deacetylase InhibitorsMicroRNAsNeoplasm ProteinsPlatelet-Derived Growth FactorProtein Kinase InhibitorsReceptors, Platelet-Derived Growth Factor

Identifiers

PMID23023716
PMCPMC3461903

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.