Author:
Bruno Benedetto,Wäsch Ralph,Engelhardt Monika,Gay Francesca,Giaccone Luisa,D’Agostino Mattia,Rodríguez-Lobato Luis-Gerardo,Danhof Sophia,Gagelmann Nico,Kröger Nicolaus,Popat Rakesh,Van de Donk Niels W.C.J.,Terpos Evangelos,Dimopoulos Meletios A.,Sonneveld Pieter,Einsele Hermann,Boccadoro Mario
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.
Publisher
Ferrata Storti Foundation (Haematologica)
Cited by
30 articles.
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