Evidence map›Paper›PMID 24481942›Full record

ReviewInternational journal of hematology2014

Peripheral T cell lymphoma in Asia.

Sanghui Park, Young Hyeh Ko

Abstract readReview
PubMed Publisher
In one paragraph

Review in International journal of hematology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 1 pooled it
–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

27 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  14. How to Sequence Therapies in Peripheral T Cell Lymphoma.Current treatment options in oncology · 2021
    Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors.

Sanghui ParkDepartment of Pathology and Global Top 5 Research Program, Ewha Womans University School of Medicine, Seoul, Republic of Korea.
Young Hyeh Ko

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral T-cell lymphomas (PTCLs) comprise a heterogeneous group of mature T- and NK-cell neoplasms, the incidence of which is higher in Asian countries than in Western countries. Although its etiology is mainly unknown, several risk factors (such as genetic factors, abnormal immunity, environmental factors, and infectious causes) have been proposed. PTCL are classified based on a combination of several parameters, including morphology, site of presentation, viral status, immunophenotype, and specific genetic alterations. Their classification is ongoing, with the emergence of new entities and refinement of existing entities because of the development of diagnostic markers and new genetic alterations. This review presents epidemiologic data for PTCL in Asia, together with recent progress in the pathology of PTCL compared with the WHO 2008 classification.

Indexed as

Anaplastic Lymphoma KinaseAsiaGastrointestinal NeoplasmsHerpesvirus 4, HumanHumansIncidenceKiller Cells, NaturalLymphoma, T-Cell, PeripheralLymphoproliferative DisordersReceptor Protein-Tyrosine KinasesRisk FactorsSkin NeoplasmsT-LymphocytesWorld Health OrganizationAnaplastic Lymphoma KinaseReceptor Protein-Tyrosine Kinases

Identifiers

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.