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  3. Therapy-Related Acute Myeloid Leukemia after CAR-T Cell Therapy with Brexucabtagene Autoleucel for Mantle Cell Lymphoma.
 

Therapy-Related Acute Myeloid Leukemia after CAR-T Cell Therapy with Brexucabtagene Autoleucel for Mantle Cell Lymphoma.

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BORIS DOI
10.48620/76115
Date of Publication
2024
Publication Type
Article
Division/Institute

Clinic of Medical Onc...

Institute of Tissue M...

Clinic of Haematology...

Department for BioMed...

Author
Volery, François
Clinic of Medical Oncology
Banz, Yaraorcid-logo
Institute of Tissue Medicine and Pathology, Clinical Pathology
Institute of Tissue Medicine and Pathology
Heini, Alexander
Clinic of Medical Oncology
Kronig, Marie-Noëlle
Clinic of Medical Oncology
Siegrist, Daniel
Clinic of Haematology and Central Haematological Laboratory
Daskalakis, Michael
Department for BioMedical Research, Forschungsgruppe Hämatologie (Erwachsene)
Clinic of Haematology and Central Haematological Laboratory
Bacher, Ulrike
Clinic of Haematology and Central Haematological Laboratory
Pabst, Thomas
Clinic of Medical Oncology
Department for BioMedical Research (DBMR)
Series
Case Reports in Oncology
ISSN or ISBN (if monograph)
1662-6575
Publisher
Karger Publishers
Language
English
Publisher DOI
10.1159/000541256
PubMed ID
39474550
Uncontrolled Keywords

Acute erythroid leuke...

Acute myeloid leukemi...

Brexucabtagene autole...

CAR-T

Mantle cell lymphoma

Description
Introduction
The introduction of CAR-T cell treatment for relapsed/refractory (r/r) mantle cell lymphoma improved survival rates of these patients. Along with its introduction in clinical routine, long-term events after CAR-T cell treatment are increasingly emerging.Case Presentation
We report the case of a patient developing acute erythroid leukemia with biallelic TP53 inactivation occurring 26 months after CAR-T therapy with brexucabtagene autoleucel (brexu-cel) for r/r mantle cell lymphoma. The patient presented with a healthy bone marrow prior to lymphoma treatments.Discussion
Secondary malignancies seem more frequent after CAR-T therapies. More studies are needed to assess potential long-term toxicities of CAR-T cell therapies including the frequency of secondary myeloid malignancies.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/188820
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
000541256.pdftextAdobe PDF1011.53 KBpublishedOpen
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