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Updated: Apr 25, 2026
![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
Precision therapy for lymphoma--current state and future directions
Andrew M Intlekofer1, Anas Younes1
1Lymphoma Service, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, Box 330, New York, NY 10065, USA.
Abstract:
Modern advances in genomics and cancer biology have produced an unprecedented body of knowledge regarding the molecular pathogenesis of lymphoma. The diverse histological subtypes of lymphoma are molecularly heterogeneous, and most likely arise from distinct oncogenic mechanisms. In parallel to these advances in lymphoma biology, several new classes of molecularly targeted agents have been developed with varying degrees of efficacy across the different types of lymphoma. In general, the development of new drugs for treating lymphoma has been mostly empiric, with a limited knowledge of the molecular target, its involvement in the disease, and the effect of the drug on the target. Thus, the variability observed in clinical responses likely results from underlying molecular heterogeneity. In the era of personalized medicine, the challenge for the treatment of patients with lymphoma will involve correctly matching a molecularly targeted therapy to the unique genetic and molecular composition of each individual lymphoma. In this Review, we discuss current and emerging biomarkers that can guide treatment decisions for patients with lymphoma, and explore the potential challenges and strategies for making biomarker-driven personalized medicine a reality in the cure and management of this disease.
Insights
Advances in genomics reveal lymphoma
Area of Science:
- Genomics and Cancer Biology
- Molecular Pathogenesis of Lymphoma
Background:
- Lymphoma subtypes are molecularly diverse, originating from distinct oncogenic mechanisms.
- New targeted therapies show variable efficacy due to limited understanding of molecular targets and disease involvement.
Purpose of the Study:
- To review current and emerging biomarkers for guiding lymphoma treatment decisions.
- To explore strategies for implementing biomarker-driven personalized medicine in lymphoma management.
Main Methods:
- Review of modern advances in genomics and cancer biology.
- Analysis of molecularly targeted agents and their clinical efficacy.
- Discussion of biomarker-driven personalized medicine approaches.
Main Results:
- Molecular heterogeneity underlies variable clinical responses to lymphoma therapies.
- Biomarkers are crucial for matching targeted therapies to individual lymphoma molecular profiles.
Conclusions:
- Personalized medicine requires matching targeted therapies to specific lymphoma molecular compositions.
- Biomarker-driven strategies are essential for advancing lymphoma cure and management.
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