Information on NKTCL1

Basic details

Name: NK/T-cell lymphomas 1 | Acronym: NKTCL1
Alt. names: peripheral T-cell lymphomas

Gene: STAT3 | MOI: Somatic | Mechanism of action: Gain of Function

No. of cases in DB: 9 | First reported in: 2013

Last updated on: 2023-04-24 15:58:51 by Xiao P. Peng

OMIM:

Orphanet: 512017

MONDO: -

DOID: -

ClinGen:

Description

Somatic activating mutations in STAT3 have been found in people with anaplastic large T-cell lymphomas or not-specified peripheral T-cell lymphomas (PMID:23563237), NK/T-cell lymphomas (PMID:25586472) or peripheral gamma-delta-T-cell derived lymphomas (PMID:25586472).

Management

Description of management option has not been reviewed yet.

9 reported cases added to GenIA

SubjectID Sex Fam.ID AD AFM Validity Country Population Reference & Pub.code
104329arrow icon U 215468 Definitive PMID:25586472 [S614R]
104330arrow icon U 215469 Definitive PMID:25586472 [D661Y]
104331arrow icon U 215470 Definitive PMID:25586472 [A702T]
107122arrow icon U 216341 Definitive PMID:25586472 [G618R]
107123arrow icon U 216342 Definitive PMID:25586472 [Y640F]
107134arrow icon M 216353 73 Definitive U.S.A. PMID:23563237 [ALCL-1]
107135arrow icon M 216354 74 Definitive U.S.A. PMID:23563237 [ALCL-2]
107136arrow icon M 216355 66 Definitive U.S.A. PMID:23563237 [PTCL-1]
107137arrow icon F 216356 33 Definitive U.S.A. PMID:23563237 [PTCL-2]

AD: Age at genetic diagnosis; AFM: age at first manifestation; PMID: PubMed ID; GRID: GenIA reference ID (ref. not in PubMed).

Summary of clinical findings

[Considering only Definitive and Possible cases]

Rank Clinical term Present Absent Unreported
1 Non-Hodgkin lymphomaarrow icon 9 (99.9%) 0 (0.0%) 0 (0.0%)
2 NK/T-cell lymphomaarrow icon 3 (33.3%) 0 (0.0%) 6 (66.7%)
3 gamma-delta-T-cell derived lymphomaarrow icon 2 (22.2%) 0 (0.0%) 7 (77.8%)
4 T-cell lymphomaarrow icon 2 (22.2%) 0 (0.0%) 7 (77.8%)
5 Anaplastic large-cell lymphomaarrow icon 2 (22.2%) 0 (0.0%) 7 (77.8%)

Summary of treatment outcomes

[Considering only Definitive and Possible cases]

Treatment ⓘ Responses & clinical indications