Evidence map›Paper›PMID 24510453›Full record

ReviewInternational journal of hematology2014

From empiric to mechanism-based therapy for peripheral T cell lymphoma.

Andrew M Intlekofer, Anas Younes

Open access · bronzeAbstract 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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

9 citing papers in PubMed, 17 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

2 authors at 1 institution in 1 country.

Andrew M IntlekoferDepartment of Medicine, Lymphoma Service, Memorial Sloan Kettering Cancer Center, 1275 York Ave, Box 330, New York, NY, 10065, USA.
Anas Younes
Memorial Sloan Kettering Cancer Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Peripheral T cell lymphoma (PTCL) represents a heterogeneous group of mature T and natural killer cell-derived neoplasms, comprising approximately 10 % of non-Hodgkin lymphoma. Although at least 20 distinct histologic subtypes of PTCL have been identified, the historical treatment approach has been uniform application of anthracycline-based combination chemotherapy, resulting in significantly inferior outcomes compared to B-cell non-Hodgkin lymphoma. Because of the generally poor outcomes with conventional chemotherapy, PTCL represents an unmet medical need, therefore providing the opportunity to evaluate novel agents. Herein, we will review the evolving treatment strategies for PTCL, discuss how different treatment approaches impact the underlying biology of PTCL, and speculate on future targets for therapeutic intervention. We conclude that future efforts to develop effective therapies for PTCL will benefit from a biomarker-driven strategy rather than histologic classification.

Indexed as

Molecular Targeted TherapyAnaplastic Lymphoma KinaseBiomarkers, TumorBrentuximab VedotinChemokinesEpigenesis, GeneticHistone DeacetylasesHumansImmunoconjugatesJanus KinasesKi-1 AntigenKiller Cells, NaturalLymphoma, T-Cell, PeripheralReceptor Protein-Tyrosine KinasesSTAT Transcription FactorsT-LymphocytesAnaplastic Lymphoma KinaseBiomarkers, TumorBrentuximab VedotinChemokinesHistone DeacetylasesImmunoconjugatesJanus KinasesKi-1 AntigenReceptor Protein-Tyrosine KinasesSTAT Transcription Factors

Identifiers

PMID24510453
OpenAlexW2033765218

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.