Evidence map›Paper›PMID 35204500›Full record

ReviewDiagnostics (Basel, Switzerland)2022

Update on Molecular Diagnosis in Extranodal NK/T-Cell Lymphoma and Its Role in the Era of Personalized Medicine.

Ka-Hei Murphy Sun, Yin-Ting Heylie Wong, Ka-Man Carmen Cheung, Carmen Michelle Yuen, Yun-Tat Ted Chan, Wing-Yan Jennifer Lai, Chun David Chao, Wing-Sum Katie Fan, Yuen-Kiu Karen Chow, Man-Fai Law and 1 more

Open access · goldAbstract readReview
In one paragraph

Review in Diagnostics (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 13 citations in OpenAlex.

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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

11 authors at 1 institution in 1 country.

Ka-Hei Murphy SunDivision of Hematopathology, Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, Hong Kong.
Yin-Ting Heylie WongDepartment of Chemical Pathology, Prince of Wales Hospital, Hong Kong.
Ka-Man Carmen CheungDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Hong Kong.
Carmen Michelle YuenDivision of Hematopathology, Department of Anatomical and Cellular Pathology, Prince of Wales Hospital, Hong Kong.
Yun-Tat Ted ChanDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Hong Kong.
Wing-Yan Jennifer LaiDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Hong Kong.
Chun David ChaoDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Hong Kong.
Wing-Sum Katie FanDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Hong Kong.
Yuen-Kiu Karen ChowDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Hong Kong.
Man-Fai LawDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Hong Kong.ORCID 0000-0003-2462-6625
Ho-Chi Tommy TamDepartment of Medicine and Therapeutics, Prince of Wales Hospital, Hong Kong.
Prince of Wales Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Natural killer (NK)/T-cell lymphoma (NKTCL) is an aggressive malignancy with unique epidemiological, histological, molecular, and clinical characteristics. It occurs in two pathological forms, namely, extranodal NKTCL (ENKTCL) and aggressive NK leukemia, according to the latest World Health Organization (WHO) classification. Epstein-Barr virus (EBV) infection has long been proposed as the major etiology of lymphomagenesis. The adoption of high-throughput sequencing has allowed us to gain more insight into the molecular mechanisms of ENKTCL, which largely involve chromosome deletion and aberrations in Janus kinase (JAK)-signal transducer and activator of transcription (STAT), programmed cell death protein-1 (PD-1)/PD-ligand 1 (PD-L1) pathways, as well as mutations in tumor suppressor genes. The molecular findings could potentially influence the traditional chemoradiotherapy approach, which is known to be associated with significant toxicity. This article will review the latest molecular findings in NKTCL and recent advances in the field of molecular diagnosis in NKTCL. Issues of quality control and technical difficulties will also be discussed, along with future prospects in the molecular diagnosis and treatment of NKTCL.

Indexed as

brentuximab vedotinEBVENKTCLimmune checkpoint inhibitorsmolecular diagnosisNGS

Identifiers

PMID35204500
PMCPMC8871212
OpenAlexW4210315710

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.