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New targets for CAR T therapy in hematologic malignancies
Affiliation:1. Department of Hematology, Cancer Center Amsterdam, Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam, Netherlands;2. Levine Cancer Institute, Atrium Health, Charlotte, NC, USA;3. Department of Haematology, University College London, London, UK;1. Department of Haematology, Singapore General Hospital, Outram Road, Singapore 169608, Singapore;2. Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, 1515 Holcombe Blvd, Houston, TX 77030, United States;1. Division of Hematology/Oncology, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, United States;2. Glioblastoma Translational Center of Excellence, Abramson Cancer Center of the University of Pennsylvania, Philadelphia, PA 19104, United States;3. Department of Neurosurgery, University of Pennsylvania Perelman School of Medicine, Philadelphia, PA 19104, United States;1. Celyad, Mont-Saint-Guibert, Belgium;2. Medical Oncology Clinic, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium;3. Department of Radiology, Institut Jules Bordet, Université Libre de Bruxelles, Brussels, Belgium;4. Institut Roi Albert II, Service d’Oncologie Médicale, Cliniques Universitaires Saint-Luc and Institut de Recherche Clinique et Expérimentale (Pole MIRO), Université Catholique de Louvain, Belgium;5. Service d’Oncologie-Hématologie, Site Notre-Dame, Grand Hôpital de Charleroi (GHdC), Belgium;6. Roswell Park Comprehensive Cancer Center, Buffalo, NY, United States;7. H Lee Moffitt Cancer Center and Research Inst, Tampa, FL, United States;8. Ghent University Hospital, Ghent, Belgium;9. Celyad, New York, NY, United States
Abstract:As we expand our acumen of the intricacies of hematological malignancies at a genetic and cellular level, we have paved the way in advancing novel targeted therapeutic avenues such as chimeric antigen receptor T-cell therapies (CAR T). Engineering cells to target a specific antigen has led to dramatic remission rates in cases of relapsed/refractory non-Hodgkin lymphoma, acute lymphoblastic leukemia as well as multiple myeloma thus far with trials in place to further advance targeted therapies in other hematological malignancies. Most currently available CAR T therapies target CD19 antigen. Studies are underway exploring novel CAR T products aimed at other tumor-specific antigens with potential to improve the efficacy and reduce the toxicities. Early studies have confirmed safety and efficacy of CD22 and BCMA targeted CAR T therapies. Moreover, various other targets including CD20, CD30, CD123, kappa, and lambda light chains among others are under clinical investigation as potential avenues of targeted therapy. This review highlights the shift in the treatment paradigm in pursuing diverse antigen targets while addressing the challenges in terms of the efficacy and toxicity of current CAR T-cell therapies.
Keywords:Cellular therapy  Hematology  Chimeric antigen receptor  Lymphoma  Myeloma  Acute leukemia
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