Evidence map›Paper›PMID 24839807›Full record

ReviewOncology (Williston Park, N.Y.)2014

Appropriate management of molecular subtypes of diffuse large B-cell lymphoma.

Kieron Dunleavy, Wyndham H Wilson

Abstract readReview
In one paragraph

Review in Oncology (Williston Park, N.Y.), 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Trial
  2. Review
  3. Article
  4. Genetic mechanisms of HLA-I loss and immune escape in diffuse large B cell lymphoma.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Kieron Dunleavy
Wyndham H Wilson

Funding

LYMPHOMA STUDIESZ01SC006741 · SC · DIVISION OF CLINICAL SCIENCES - NCI · PI WILSON, WYNDHAM H · 1996 to 2008
$893k
Intramural NIH HHS Z01 SC006741
6 · The paper itself

Abstract

In recent years, we have made huge strides in our understanding of the molecular complexity of diffuse large B-cell lymphoma (DLBCL). New technologies, such as gene expression profiling, RNA interference screening, and DNA sequencing, have identified several new signaling pathways and therapeutic targets for drug development. While we once considered DLBCL to be a single disease entity, recent insights have helped identify the existence of at least three distinct molecular diseases: a germinal center B-cell-like subtype, an activated B-cell-like subtype, and a primary mediastinal B-cell lymphoma subtype. All three subtypes originate from different stages of B-cell differentiation and are characterized by distinct mechanisms of oncogenic activation. This classification of DLBCL has laid the foundation for the development of new agents and novel strategies that target individual subtypes.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsGene Expression ProfilingHumansLymphoma, Large B-Cell, DiffuseMolecular Targeted TherapySurvival Analysis

Identifiers

PMID24839807
PMCPMC7722987

What OpenQuestion holds

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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.