| Literature DB >> 30576834 |
Ankit J Kansagra1, Noelle V Frey2, Merav Bar3, Theodore W Laetsch4, Paul A Carpenter3, Bipin N Savani5, Helen E Heslop6, Catherine M Bollard7, Krishna V Komanduri8, Dennis A Gastineau9, Christian Chabannon10, Miguel A Perales11, Michael Hudecek12, Mahmoud Aljurf13, Leslie Andritsos14, John A Barrett15, Veronika Bachanova16, Chiara Bonini17, Armin Ghobadi18, Saar I Gill2, Joshua Hill3, Saad Kenderian19, Partow Kebriaei20, Arnon Nagler21, David Maloney3, Hien D Liu22, Nirali N Shah23, Mohamed A Kharfan-Dabaja24, Elizabeth J Shpall20, Ghulam J Mufti25, Laura Johnston26, Elad Jacoby21, Ali Bazarbachi27, John F DiPersio18, Steven Z Pavletic28, David L Porter2, Stephan A Grupp29, Michel Sadelain30, Mark R Litzow31, Mohamad Mohty32, Shahrukh K Hashmi33.
Abstract
On August 30, 2017 the US Food and Drug Administration approved tisagenlecleucel (Kymriah; Novartis, Basel, Switzerland), a synthetic bioimmune product of anti-CD19 chimeric antigen receptor T cells (CAR-T), for the treatment of children and young adults with relapsed/refractory B cell acute lymphoblastic leukemia (B-ALL). With this new era of personalized cancer immunotherapy, multiple challenges are present, ranging from implementation of a CAR-T program to safe delivery of the drug, long-term toxicity monitoring, and disease assessments. To address these issues experts representing the American Society for Blood and Marrow Transplant, the European Society for Blood and Marrow Transplantation, the International Society of Cell and Gene Therapy, and the Foundation for the Accreditation of Cellular Therapy formed a global CAR-T task force to identify and address key questions pertinent for hematologists and transplant physicians regarding the clinical use of anti CD19 CAR-T therapy in patients with B-ALL. This article presents an initial roadmap for navigating common clinical practice scenarios that will become more prevalent now that the first commercially available CAR-T product for B-ALL has been approved.Entities:
Keywords: Chimeric antigen receptor; Leukemia; T cell
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Year: 2018 PMID: 30576834 PMCID: PMC8335749 DOI: 10.1016/j.bbmt.2018.12.068
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742