Unknown

Dataset Information

0

Chimeric Antigen Receptor (CAR) T Cell Therapy in Acute Myeloid Leukemia (AML).


ABSTRACT: Despite high response rates after initial chemotherapy in patients with acute myeloid leukemia (AML), relapses occur frequently, resulting in a five-year-survival by <30% of the patients. Hitherto, allogeneic hemotopoietic stem cell transplantation (allo-HSCT) is the best curative treatment option in intermediate and high risk AML. It is the proof-of-concept for T cell-based immunotherapies in AML based on the graft-versus-leukemia (GvL)-effect, but it also bears the risk of graft-versus-host disease. CD19-targeting therapies employing chimeric antigen receptor (CAR) T cells are a breakthrough in cancer therapy. A similar approach for myeloid malignancies is highly desirable. This article gives an overview on the state-of-the art of preclinical and clinical studies on suitable target antigens for CAR T cell therapy in AML patients.

SUBMITTER: Hofmann S 

PROVIDER: S-EPMC6406805 | biostudies-literature | 2019 Feb

REPOSITORIES: biostudies-literature

altmetric image

Publications

Chimeric Antigen Receptor (CAR) T Cell Therapy in Acute Myeloid Leukemia (AML).

Hofmann Susanne S   Schubert Maria-Luisa ML   Wang Lei L   He Bailin B   Neuber Brigitte B   Dreger Peter P   Müller-Tidow Carsten C   Schmitt Michael M  

Journal of clinical medicine 20190206 2


Despite high response rates after initial chemotherapy in patients with acute myeloid leukemia (AML), relapses occur frequently, resulting in a five-year-survival by <30% of the patients. Hitherto, allogeneic hemotopoietic stem cell transplantation (allo-HSCT) is the best curative treatment option in intermediate and high risk AML. It is the proof-of-concept for T cell-based immunotherapies in AML based on the graft-versus-leukemia (GvL)-effect, but it also bears the risk of graft-versus-host di  ...[more]

Similar Datasets

| S-EPMC7761730 | biostudies-literature
| S-EPMC8815830 | biostudies-literature
| S-EPMC9809466 | biostudies-literature
| S-EPMC10660693 | biostudies-literature
| S-EPMC8833567 | biostudies-literature
| S-EPMC5576380 | biostudies-literature
| S-EPMC7941581 | biostudies-literature
| S-EPMC8310147 | biostudies-literature
| S-EPMC9387679 | biostudies-literature
| S-EPMC8930424 | biostudies-literature