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

被引:0
作者
Lee, Ju Hyeong [1 ]
Gu, Ja-Yoon [2 ]
Lee, Jee-Soo [1 ]
Kim, Seon Young [1 ]
Chang, Yoon Hwan [1 ]
Seong, Moon-Woo [1 ]
Yun, Hongseok [3 ]
Kim, Hyun Kyung [1 ,2 ]
机构
[1] Seoul Natl Univ, Coll Med, Dept Lab Med, Seoul, South Korea
[2] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul, South Korea
[3] Seoul Natl Univ Hosp, Dept Genom Med, Seoul, South Korea
关键词
Aggressive NK-cell Leukemia; Extranodal NK/T-cell lymphoma; Bone marrow neoplasms; Next generation sequencing; FAT1; NATURAL-KILLER-CELL; COMPARATIVE GENOMIC HYBRIDIZATION; NASAL-TYPE; SURFACE PHENOTYPE; LINEAGE; DIAGNOSIS; LEUKAEMIA/LYMPHOMA; LYMPHOMA/LEUKEMIA; IDENTIFICATION; DISORDERS;
D O I
10.1038/s41598-025-05843-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
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.
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页数:11
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