Molecular Complexity of Diffuse Large B-Cell Lymphoma: Can It Be a Roadmap for Precision Medicine?
Nicoletta CoccaroLuisa AnelliAntonella ZagariaTommasina PerroneGiorgina SpecchiaFrancesco AlbanoPublished in: Cancers (2020)
Diffuse large B-cell lymphoma (DLBCL) is the most common non-Hodgkin lymphoma; it features extreme molecular heterogeneity regardless of the classical cell-of-origin (COO) classification. Despite this, the standard therapeutic approach is still immunochemotherapy (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone-R-CHOP), which allows a 60% overall survival (OS) rate, but up to 40% of patients experience relapse or refractory (R/R) disease. With the purpose of searching for new clinical parameters and biomarkers helping to make a better DLBCL patient characterization and stratification, in the last years a series of large discovery genomic and transcriptomic studies has been conducted, generating a wealth of information that needs to be put in order. We reviewed these researches, trying ultimately to understand if there are bases offering a roadmap toward personalized and precision medicine also for DLBCL.
Keyphrases
- diffuse large b cell lymphoma
- epstein barr virus
- single cell
- end stage renal disease
- newly diagnosed
- ejection fraction
- chronic kidney disease
- machine learning
- small molecule
- low dose
- free survival
- prognostic factors
- peritoneal dialysis
- deep learning
- case report
- stem cells
- high throughput
- high dose
- drug delivery
- cell therapy
- health information
- patient reported outcomes
- mesenchymal stem cells
- patient reported