Related Experiment Video
Updated: Mar 11, 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)
09:34
Dynamic Imaging of Chimeric Antigen Receptor T Cells with [18F]Tetrafluoroborate Positron Emission Tomography/Computed Tomography
Published on: February 17, 2022
3.9K
Promising Novel Agents for Aggressive B-Cell Lymphoma
1Lymphoma Service, Memorial Sloan Kettering Cancer Center, 1275 York Avenue, New York, NY 10021, USA.
Hematology/Oncology Clinics of North America
|November 28, 2016
Summary
Diffuse large B-cell lymphoma (DLBCL) remains a common cancer. While rituximab has been a standard treatment since 2006, new agents are in development to improve patient cure rates.
Area of Science:
- Oncology
- Hematology
Background:
- Diffuse large B-cell lymphoma (DLBCL) is the most prevalent lymphoma subtype in Western countries.
- Current treatments achieve cure rates of 50%–60% for DLBCL patients.
- Rituximab, approved in 2006, is a standard first-line therapy combined with chemotherapy, with no new agents approved since.
Purpose of the Study:
- To review recent data on novel therapeutic agents under investigation for DLBCL treatment.
- To highlight promising new drugs that may improve outcomes for DLBCL patients.
Main Methods:
- Literature review of recent clinical trial data.
- Analysis of emerging agents in the treatment pipeline for DLBCL.
Main Results:
- Several novel agents demonstrate promising efficacy in early-phase clinical trials.
- These agents target different pathways involved in DLBCL pathogenesis.
- Combinatorial approaches are being explored to enhance treatment effectiveness.
Conclusions:
- There is a significant unmet need for improved DLBCL therapies.
- Emerging agents represent a promising frontier for enhancing cure rates in DLBCL.
- Further clinical investigation is warranted to establish the role of these new treatments.

