New biomarkers and therapeutic strategies in acute lymphoblastic leukemias: Recent advances.
Carolina SimioniFabio BergaminiMartina FerioliErika RimondiLorenzo CarusoLuca M NeriPublished in: Hematological oncology (2019)
Acute lymphoblastic leukemia (ALL) represents a heterogeneous group of hematologic malignancies, and it is normally characterized by an aberrant proliferation of immature lymphoid cells. Moreover, dysregulation of multiple signaling pathways that normally regulate cellular transcription, growth, translation, and proliferation is frequently encountered in this malignancy. ALL is the most frequent tumor in childhood, and adult ALL patients still correlate with poor survival. This review focuses on modern therapies in ALL that move beyond standard chemotherapy, with a particular emphasis on immunotherapeutic approaches as new treatment strategies. Bi-specific T-cell Engagers (BiTE) antibodies, the chimeric antigen receptor (CAR)-T cells, or CRISPR-Cas9 (clustered regularly interspaced short palindromic repeats [CRISPR]-associated nuclease 9) represent other new innovative approaches for this disease. Target and tailored therapy could make the difference in previously untreatable cases, i.e., precision and personalized medicine. Clinical trials will help to select the most efficient novel therapies in ALL management and to integrate them with existing treatments to achieve durable cures.
Keyphrases
- crispr cas
- signaling pathway
- acute lymphoblastic leukemia
- genome editing
- induced apoptosis
- clinical trial
- end stage renal disease
- ejection fraction
- newly diagnosed
- peritoneal dialysis
- genome wide
- cell proliferation
- transcription factor
- stem cells
- randomized controlled trial
- radiation therapy
- endoplasmic reticulum stress
- childhood cancer
- dna methylation
- allogeneic hematopoietic stem cell transplantation
- bone marrow
- patient reported
- early life
- acute respiratory distress syndrome
- intensive care unit