Department of Pathology, Copenhagen University Hospital-Rigshospitalet, 2100 Copenhagen, Denmark.
Department of Ophthalmology, Copenhagen University Hospital-Rigshospitalet, 2100 Copenhagen, Denmark.
Int J Mol Sci. 2024 Mar 7;25(6):3094. doi: 10.3390/ijms25063094.
To provide insights into targetable oncogenic pathways, this retrospective cohort study investigated the genetic profile of 26 patients with diffuse large B-cell lymphoma, not otherwise specified (DLBCL-NOS), and two patients with high-grade B-cell lymphoma with and rearrangements (HGBCL) presenting in the ocular adnexa. Pathogenic variants and copy number variations in 128 B-cell lymphoma-relevant genes were analyzed by targeted next-generation sequencing. Genetic subtypes were determined with the LymphGen algorithm. Primary ocular adnexal DLBCL-NOS constituted 50% (n = 14) and was generally characterized by non-germinal center B-cell origin (non-GCB) (n = 8, 57%), and LymphGen MCD subtype (n = 5, 36%). Primary ocular adnexal DLBCL-NOS presented pathogenic variants in genes involved in NF-κB activation and genes which are recurrently mutated in other extranodal lymphomas of non-GCB origin, including (n = 4, 29%), (n = 3, 21%), (n = 3, 21%), and (n = 3, 21%). Relapsed DLBCL-NOS presenting in the ocular adnexa (n = 6) were all of non-GCB origin and frequently of MCD subtype (n = 3, 50%), presenting with a similar genetic profile as primary ocular adnexal DLBCL-NOS. These results provide valuable insights into genetic drivers in ocular adnexal DLBCL-NOS, offering potential applications in future precision medicine.
为了深入了解可靶向的致癌途径,本回顾性队列研究调查了 26 例未特指弥漫性大 B 细胞淋巴瘤(DLBCL-NOS)和 2 例伴有 和 重排的高级别 B 细胞淋巴瘤(HGBCL)患者的眼部附属器的遗传特征。通过靶向下一代测序分析了 128 个 B 细胞淋巴瘤相关基因中的致病性变异和拷贝数变异。采用 LymphGen 算法确定遗传亚型。原发性眼部附属器 DLBCL-NOS 占 50%(n=14),通常以非生发中心 B 细胞起源(non-GCB)(n=8,57%)和 LymphGen MCD 亚型(n=5,36%)为特征。原发性眼部附属器 DLBCL-NOS 存在涉及 NF-κB 激活的基因和其他非生发中心起源的结外淋巴瘤中经常发生突变的基因的致病性变异,包括 (n=4,29%)、 (n=3,21%)、 (n=3,21%)和 (n=3,21%)。眼部附属器复发的 DLBCL-NOS(n=6)均为非 GCB 起源,经常为 MCD 亚型(n=3,50%),具有与原发性眼部附属器 DLBCL-NOS 相似的遗传特征。这些结果为眼部附属器 DLBCL-NOS 的遗传驱动因素提供了有价值的见解,为未来的精准医学提供了潜在的应用。