The Genetic Profile of Large B-Cell Lymphomas Presenting in the Ocular Adnexa.
Stine Dahl VestPatrick René Gerhard EriksenFleur A de GrootRuben A L de GroenAnne H R KleijMarina Knudsen KirkegaardPeter KamperPeter Kristian RasmussenChristian von BuchwaldPeter de Nully BrownJens Folke KiilgaardJoost S P VermaatSteffen HeegaardPublished in: International journal of molecular sciences (2024)
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 MYC and BCL2 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 MYD88 (n = 4, 29%), CD79B (n = 3, 21%), PIM1 (n = 3, 21%), and TBL1XR1 (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.
Keyphrases
- diffuse large b cell lymphoma
- copy number
- genome wide
- mitochondrial dna
- epstein barr virus
- nitric oxide synthase
- dna methylation
- optic nerve
- high grade
- case report
- signaling pathway
- transcription factor
- acute lymphoblastic leukemia
- risk assessment
- inflammatory response
- mass spectrometry
- lps induced
- high resolution
- gene expression
- cancer therapy
- nk cells
- current status
- pi k akt