| Literature DB >> 33792221 |
Benedetto Bruno1, Ralph Wäsch2, Monika Engelhardt2, Francesca Gay3, Luisa Giaccone3, Mattia D'Agostino3, Luis-Gerardo Rodríguez-Lobato4, Sophia Danhof5, Nico Gagelmann6, Nicolaus Kröger6, Rakesh Popat7, Niels W C J Van de Donk8, Evangelos Terpos9, Meletios A Dimopoulos9, Pieter Sonneveld10, Hermann Einsele5, Mario Boccadoro3.
Abstract
Chimeric antigen receptor (CAR) T cells (CAR-T) have dramatically changed the treatment landscape of B-cell malignancies, providing a potential cure for relapsed/refractory patients. Long-term responses in patients with acute lymphoblastic leukemia and non Hodgkin lymphomas have encouraged further development in myeloma. In particular, B-cell maturation antigen (BCMA)-targeted CAR-T have established very promising results in heavily pre-treated patients. Moreover, CAR-T targeting other antigens (i.e., SLAMF7 and CD44v6) are currently under investigation. However, none of these current autologous therapies have been approved, and despite high overall response rates across studies, main issues such as long-term outcome, toxicities, treatment resistance, and management of complications limit as yet their widespread use. Here, we critically review the most important pre-clinical and clinical findings, recent advances in CAR-T against myeloma, as well as discoveries in the biology of a still incurable disease, that, all together, will further improve safety and efficacy in relapsed/refractory patients, urgently in need of novel treatment options.Entities:
Year: 2021 PMID: 33792221 DOI: 10.3324/haematol.2020.276402
Source DB: PubMed Journal: Haematologica ISSN: 0390-6078 Impact factor: 9.941