Cell-of-origin classification by gene expression and MYC-rearrangements in diffuse large B-cell lymphoma of children and adolescents.
Monika SzczepanowskiJonas LangeChristian W KohlerNeus Masque-SolerMartin ZimmermannSietse M AukemaMichael AltenbuchingerThorsten RehbergFriederike MahnReiner SiebertRainer SpangBirgit BurkhardtWolfram KlapperPublished in: British journal of haematology (2017)
We present the largest series of diffuse large B-cell lymphoma (DLBCL) in patients younger than 18 years analysed to date by gene expression profiling using Nanostring technology to identify molecular subtypes and fluorescent in situ hybridization for translocations of MYC. We show that the activated B cell-like subtype of DLBCL is exceedingly rare in children and - in contrast to adults- not associated with outcome. Furthermore, we review the current literature and demonstrate that MYC translocations are not more frequent in paediatric compared to adult DLBCL. A prognostic role of MYC in the paediatric age groups seems unlikely.
Keyphrases
- diffuse large b cell lymphoma
- epstein barr virus
- gene expression
- transcription factor
- intensive care unit
- emergency department
- genome wide
- ejection fraction
- newly diagnosed
- systematic review
- dna methylation
- genome wide identification
- young adults
- machine learning
- deep learning
- magnetic resonance
- stem cells
- quantum dots
- computed tomography
- copy number
- patient reported outcomes
- living cells
- mesenchymal stem cells
- childhood cancer