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Updated: Jul 4, 2025
![Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F62334.jpg&w=3840&q=50)
Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
Published on: February 17, 2022
Aggressive T-cell lymphomas: 2024: Updates on diagnosis, risk stratification, and management
Shin Yeu Ong1,2, Jasmine M Zain1
1Department of Hematology/Hematopoietic Cell Transplantation, City of Hope Medical Center, Duarte, California, USA.
Peripheral T-cell lymphomas (PTCL) have poor prognoses. Advances in molecular understanding are driving the development of targeted therapies and immunotherapies to improve PTCL treatment outcomes.
Area of Science:
- Hematology
- Oncology
- Molecular Biology
Background:
- Peripheral T-cell lymphomas (PTCL) encompass over 30 subtypes with poor prognoses.
- Histologic variations alone do not fully capture the heterogeneity of PTCL subtypes.
Purpose of the Study:
- To review the molecular pathogenesis of various PTCL subtypes.
- To discuss emerging targeted therapies and immunotherapies for PTCL treatment.
Main Methods:
- Review of gene expression profiling and molecular techniques.
- Analysis of current clinical trials for targeted agents and immunotherapies.
Main Results:
- Molecular techniques reveal distinct differences across PTCL subtypes, informing the 5th WHO classification.
- Targeted agents (e.g., brentuximab vedotin, PI3K inhibitors, HDAC inhibitors, ALK inhibitors) and immunotherapies (e.g., checkpoint inhibitors, CAR-T) show promise.
- Allogeneic stem cell transplant remains a curative option for aggressive PTCL.
Conclusions:
- Understanding PTCL molecular pathogenesis is crucial for developing effective therapies.
- Targeted agents and novel immunotherapies are essential for improving clinical outcomes in PTCL.
- Further research and clinical trials are needed to optimize treatment strategies for diverse PTCL subtypes.
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