The what, when and how of CAR T cell therapy for ALL

Chimeric Antigen Receptor (CAR) T cells that have been engineered to target CD19 have shown great promise in patients with relapsed and refractory B cell acute lymphocytic leukemia with remission rates of 70–90%. Some remissions have successfully bridged patients to a curable allogeneic stem cell tr...

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Bibliographic Details
Published inBest practice & research. Clinical haematology Vol. 30; no. 3; pp. 275 - 281
Main Author Frey, Noelle
Format Journal Article
LanguageEnglish
Published Netherlands Elsevier Ltd 01.09.2017
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ISSN1521-6926
1532-1924
1532-1924
DOI10.1016/j.beha.2017.07.009

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Summary:Chimeric Antigen Receptor (CAR) T cells that have been engineered to target CD19 have shown great promise in patients with relapsed and refractory B cell acute lymphocytic leukemia with remission rates of 70–90%. Some remissions have successfully bridged patients to a curable allogeneic stem cell transplant, some responses have been durable without further treatment, and some patients have achieved durable remissions for relapsed ALL after allogeneic stem cell transplant. Cytokine release syndrome, correlating with the in vivo activation and expansion of T cells, and neurologic toxicity are the most significant side effects and approaches to better understand and manage these events are the subject of ongoing clinical trials. The decision to intervene with CARTs requires an individualized approach taking into consideration patient, disease and therapy related factors.
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ISSN:1521-6926
1532-1924
1532-1924
DOI:10.1016/j.beha.2017.07.009