CAR T-Cells for the Treatment of B-Cell Acute Lymphoblastic Leukemia

Author:

Saleh Khalil1,Pasquier Florence2,Bigenwald Camille2,De Botton Stéphane2,Ribrag Vincent23,Castilla-Llorente Cristina2

Affiliation:

1. International Department, Gustave Roussy Cancer Campus, 94800 Villejuif, France

2. Department of Hematology, Gustave Roussy Cancer Campus, 94800 Villejuif, France

3. Département D’innovation Thérapeutique et D’essais Précoces (DITEP), Gustave Roussy Cancer Campus, 94800 Villejuif, France

Abstract

B-cell acute lymphoblastic leukemia (B-ALL) is the most common subtype of acute leukemia in the pediatric population. The prognosis and treatment of B-ALL have dramatically improved over the past decade with the adoption of intensive and prolonged combination chemotherapy regimens. The advent of novel immunologic agents such as blinatumomab and inotuzumab has changed the treatment landscape of B-ALL. However, patients have continued to relapse, raising the need for novel therapies. Chimeric antigen receptor (CAR) T-cells have achieved a milestone in the treatment of B-ALL. Two CD19-targeting CAR T-cells were approved by the Food and Drug Administration and the European Medicines Agency for the treatment of relapsed and/or refractory B-ALL. In this review, we review the available data regarding CD19-targeting CAR T-cells with their safety profile as well as the mechanism of resistance to these agents and the way to overcome this resistance.

Publisher

MDPI AG

Subject

General Medicine

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