| Literature DB >> 33363031 |
Xavier Roussel1,2, Etienne Daguindau1,2, Ana Berceanu2, Yohan Desbrosses2, Walid Warda1, Mathieu Neto da Rocha1, Rim Trad1, Eric Deconinck1,2, Marina Deschamps1, Christophe Ferrand1.
Abstract
Recent studies have provided several insights into acute myeloid leukemia. Studies based on molecular biology have identified eight functional mutations involved in leukemogenesis, including driver and passenger mutations. Insight into Leukemia stem cells (LSCs) and assessment of cell surface markers have enabled characterization of LSCs from hematopoietic stem and progenitor cells. Clonal evolution has been described as having an effect similar to that of microenvironment alterations. Such biological findings have enabled the development of new targeted drugs, including drug inhibitors and monoclonal antibodies with blockage functions. Some recently approved targeted drugs have resulted in new therapeutic strategies that enhance standard intensive chemotherapy regimens as well as supportive care regimens. Besides the progress made in adoptive immunotherapy, since allogenic hematopoietic stem cell transplantation enabled the development of new T-cell transfer therapies, such as chimeric antigen receptor T-cell and transgenic TCR T-cell engineering, new promising strategies that are investigated.Entities:
Keywords: CAR T cells; acute myeloid leukemia; clinical trials; immunotherapies; management
Year: 2020 PMID: 33363031 PMCID: PMC7757414 DOI: 10.3389/fonc.2020.599933
Source DB: PubMed Journal: Front Oncol ISSN: 2234-943X Impact factor: 6.244