ALL Maintenance Treatment for Early Loss of B-Cell Aplasia after Tisagenlecleucel Therapy

Chimeric antigen receptor (CAR) T-cell therapy is a new, effective treatment for patients with relapsed/refractory (r/r) B-cell acute lymphoblastic leukaemia (ALL). Tisagenlecleucel achieved a complete remission (CR) rate and minimal residual disease (MRD) negativity of 81% at 3 months in the pivota...

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Veröffentlicht in:Blood 2021-11, Vol.138 (Supplement 1), p.3859-3859
Hauptverfasser: Gabelli, Maria, Oporto Espuelas, Macarena, Bonney, Denise, Burridge, Saskia, Farish, Susan, Mullanfiroze, Khushnuma, Lazareva, Arina, Samarasinghe, Sujith, Ancliffe, Philip, Vora, Ajay, Bartram, Jack, Hedges, Emma, Ware, Kirsty, Young, Lindsey, Cugno, Chiara, Chenchara, Lenka, Silva, Juliana, Mirci-Danicar, Oana, Riley, Lynne, Pavasovic, Vesna, Rao, Anupama, Veys, Paul, Lucchini, Giovanna, Chiesa, Robert, Rao, Kanchan, Amrolia, Persis J, Ghorashian, Sara
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Sprache:eng
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Zusammenfassung:Chimeric antigen receptor (CAR) T-cell therapy is a new, effective treatment for patients with relapsed/refractory (r/r) B-cell acute lymphoblastic leukaemia (ALL). Tisagenlecleucel achieved a complete remission (CR) rate and minimal residual disease (MRD) negativity of 81% at 3 months in the pivotal study; overall survival (OS) was 76% at 12 months (Maude et al, 2018). Real world data confirmed similar outcomes, with 1-year OS of 77% and event free survival (EFS) of 52% (Pasquini et al, 2020). Relapse can occur in the form of CD19 negative or CD19 positive ALL. The latter is associated with lack of persistence of the CAR T product. B-cell aplasia (BCA) is an indirect measure of CAR T presence. Early (
ISSN:0006-4971
1528-0020
DOI:10.1182/blood-2021-152344