TP53 dysfunction in chronic lymphocytic leukemia: clinical relevance in the era of B-cell receptors and BCL-2 inhibitors.
Fortunato MorabitoMassimo GentilePaola MenichiniAnna Grazia RecchiaPaola MenichiniMamdouh SkafiMoien AtrashGiuseppa De LucaSabrina BossioHamdi Al-JanazrehSara GalimbertiZaidoun SalahLucio MorabitoAlham MujahedMusa HindiyehMariella DonoFranco FaisGiovanna CutronaAntonino NeriGiovanni TripepiGilberto FronzaManlio FerrariniPublished in: Expert opinion on investigational drugs (2020)
Although TP53 dysfunction has less negative influence on the new biological therapies, patients with these alterations, particularly those with biallelic inactivation of TP53, have a worst outcome with these therapies than those without alterations. At present, a determination of TP53, particularly with next generation sequencing (NGS) methodologies, may be sufficient for the identifications of the patients unsuitable for chemo-immunotherapy, although integration with del(17p) would be advisable. For the future, more extensive determinations of the TP53 status, including functional assays, may become part of the current armamentarium for a better patient stratification and treatment with newer protocols.
Keyphrases
- chronic lymphocytic leukemia
- end stage renal disease
- ejection fraction
- oxidative stress
- newly diagnosed
- chronic kidney disease
- peritoneal dialysis
- photodynamic therapy
- prognostic factors
- high throughput
- case report
- gene expression
- intellectual disability
- current status
- copy number
- dna methylation
- autism spectrum disorder
- high resolution
- cancer therapy
- locally advanced
- circulating tumor