Evidence map›Paper›PMID 40594571›Full record

ArticleScientific reports2025

Genetic and clinical distinction between aggressive NK-cell leukemia and extranodal NK/T-cell lymphoma with bone marrow involvement.

Ju Hyeong Lee, Ja-Yoon Gu, Jee-Soo Lee, Seon Young Kim, Yoon Hwan Chang, Moon-Woo Seong, Hongseok Yun, Hyun Kyung Kim

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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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

2 citing papers in PubMed.

  1. Epstein-Barr Virus-Associated T/NK-Cell Neoplasms.Journal of medical virology · 2026
    Review
  2. Article
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

8 authors.

Ju Hyeong LeeDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Ja-Yoon GuCancer Research Institute, Seoul National University College of Medicine, Seoul, Korea.
Jee-Soo LeeDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Seon Young KimDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Yoon Hwan ChangDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Moon-Woo SeongDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea.
Hongseok YunDepartment of Genomic Medicine, Seoul National University Hospital, Seoul, Korea.
Hyun Kyung KimDepartment of Laboratory Medicine, Seoul National University College of Medicine, Seoul, Korea. lukekhk@snu.ac.kr.

Funding

Korean government HX23C1718
6 · The paper itself

Abstract

Aggressive NK-cell leukemia (ANKL) shares common clinicopathological features with extranodal NK/T-cell lymphoma with bone marrow (BM) involvement (ENKTL-BM), making their distinction challenging in BM examination. Despite numerous studies, genetic differences between the two diseases remained largely unclear. To investigate the genetic and clinical differences between ANKL and ENKTL-BM, we performed targeted sequencing of 282 genes and survival analyses on 15 ANKL and 5 ENKTL-BM patients. Mutation frequency of FAT family genes was higher in ANKL than in ENKTL-BM (80.0% vs. 0.0%, P = 0.004), and FAT1 gene mutations were associated with significantly lower survival rates in ANKL patients (P = 0.002). Copy number alterations including 11q loss and 4q loss were detected exclusively in ANKL. The interval from symptom onset to death was significantly shorter (113.0 vs. 440.5 days, P = 0.027) and survival rate was significantly lower (P = 0.004) in ANKL than in ENKTL-BM. In conclusion, ANKL exhibited a higher mutation frequency of FAT family genes, a more acute fulminant clinical course, and worse prognosis than ENKTL-BM, indicating that ANKL and ENKTL-BM can be distinguished both genetically and clinically. We expect the identified FAT1 gene mutations to serve as novel prognostic factors for ANKL.

Indexed as

Bone MarrowLeukemia, Large Granular LymphocyticLymphoma, Extranodal NK-T-CellAdultAgedCadherinsDNA Copy Number VariationsFemaleHumansMaleMiddle AgedMutationPrognosisYoung AdultCadherinsFAT1 protein, humanAggressive NK-cell LeukemiaBone marrow neoplasmsExtranodal NK/T-cell lymphomaFAT1Next generation sequencing

Identifiers

PMID40594571
PMCPMC12219632

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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.