Ontology highlight
ABSTRACT: Significance
T-ALL is driven by oncogenic transcription factors that act along with secondary acquired mutations. These lesions, together with active signaling pathways, may be targeted by therapeutic agents. Bridging research and clinical practice can accelerate the testing of novel treatments in clinical trials, offering an opportunity for patients with poor outcome.
SUBMITTER: Cordo' V
PROVIDER: S-EPMC8447273 | biostudies-literature | 2021 Jan
REPOSITORIES: biostudies-literature
Cordo' Valentina V van der Zwet Jordy C G JCG Canté-Barrett Kirsten K Pieters Rob R Meijerink Jules P P JPP
Blood cancer discovery 20201124 1
T-cell acute lymphoblastic leukemia (T-ALL) is an aggressive hematologic malignancy characterized by aberrant proliferation of immature thymocytes. Despite an overall survival of 80% in the pediatric setting, 20% of patients with T-ALL ultimately die from relapsed or refractory disease. Therefore, there is an urgent need for novel therapies. Molecular genetic analyses and sequencing studies have led to the identification of recurrent T-ALL genetic drivers. This review summarizes the main genetic ...[more]