Language

English

Publication Date

12-1-2022

Journal

Best Practice & Research Clinical Haematology | Journal

DOI

10.1016/j.beha.2022.101414

PMID

36517124

PMCID

PMC10683866

PubMedCentral® Posted Date

12-1-2023

PubMedCentral® Full Text Version

Author MSS

Abstract

Autologous T cells genetically modified with a CD19 chimeric antigen receptor are an effective therapy for children and adults with relapsed or refractory acute lymphoblastic leukemia with initial response rates ranging from 70 to 85%. Unfortunately, about half of these responding patients will subsequently relapse raising the question of whether allogeneic hemopoietic stem cell transplant should be considered as a consolidative therapy. Currently efforts are focused on defining risk factors for relapse to try and develop algorithms predicting which patients may benefit from allogenic transplant.

Keywords

Child, Adult, Humans, Receptors, Chimeric Antigen, Immunotherapy, Adoptive, Antigens, CD19, Precursor Cell Lymphoblastic Leukemia-Lymphoma, Hematopoietic Stem Cell Transplantation, Recurrence, Chimeric antigen receptor, Acute Lymphoblastic Leukemia, Allogeneic Stem Cell Transplant

Published Open-Access

yes

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