Next-Generation Sequencing in Acute Lymphoblastic Leukemia.
Nicoletta CoccaroLuisa AnelliAntonella ZagariaGiorgina SpecchiaFrancesco AlbanoPublished in: International journal of molecular sciences (2019)
Acute lymphoblastic leukemia (ALL) is the most common childhood cancer and accounts for about a quarter of adult acute leukemias, and features different outcomes depending on the age of onset. Improvements in ALL genomic analysis achieved thanks to the implementation of next-generation sequencing (NGS) have led to the recent discovery of several novel molecular entities and to a deeper understanding of the existing ones. The purpose of our review is to report the most recent discoveries obtained by NGS studies for ALL diagnosis, risk stratification, and treatment planning. We also report the first efforts at NGS use for minimal residual disease (MRD) assessment, and early studies on the application of third generation sequencing in cancer research. Lastly, we consider the need for the integration of NGS analyses in clinical practice for genomic patients profiling from the personalized medicine perspective.
Keyphrases
- acute lymphoblastic leukemia
- childhood cancer
- copy number
- young adults
- end stage renal disease
- clinical practice
- allogeneic hematopoietic stem cell transplantation
- ejection fraction
- chronic kidney disease
- single cell
- healthcare
- primary care
- newly diagnosed
- small molecule
- quality improvement
- papillary thyroid
- prognostic factors
- peritoneal dialysis
- case control
- squamous cell carcinoma
- type diabetes
- gene expression
- dna methylation
- circulating tumor
- single molecule
- skeletal muscle
- respiratory failure
- acute myeloid leukemia
- acute respiratory distress syndrome
- lymph node metastasis
- insulin resistance