Related Experiment Video
Updated: Jun 16, 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
Novel agents for B-cell non-Hodgkin lymphoma: science and the promise
Kevin Tay1, Kieron Dunleavy, Wyndham H Wilson
1Center for Cancer Research, National Cancer Institute, National Institutes of Health, 10 Centre Drive, Bethesda, MD 20892-1203, USA.
Abstract:
There has been tremendous insight gained in the last two decades from basic science research. New molecular targets in neoplastic cells are emerging and provide the rationale for clinical development of novel agents in non-Hodgkin lymphoma. These novel agents can be broadly categorized into two groups. The first is by immunotherapy which includes novel monoclonal antibodies and immunomodulating drugs, which takes advantage of or optimizes immune system function. The other group of drugs target small molecules that may play an important role in tumorigenesis. The mechanisms of anti-tumor activity include targeting apoptotic pathways, inhibition of proteasomes, mammalian target of rapamycin (mTOR), cyclin-dependent kinases and histone deacetylases. The purpose of this review is to focus on these novel agents and the various treatment approaches that are currently being evaluated in non-Hodgkin lymphoma.
Insights
Novel therapies for non-Hodgkin lymphoma are emerging from basic science research. This review covers new immunotherapies and small molecule drugs targeting key cancer pathways.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Recent advances in basic science research have identified new molecular targets in neoplastic cells.
- These discoveries provide a foundation for developing novel therapeutic agents for non-Hodgkin lymphoma (NHL).
Purpose of the Study:
- To review novel therapeutic agents and treatment strategies currently under investigation for non-Hodgkin lymphoma.
- To categorize these agents based on their mechanisms of action and therapeutic approach.
Main Methods:
- Literature review of recent scientific publications and clinical trial data.
- Categorization of novel agents into immunotherapy and small molecule inhibitors.
- Analysis of anti-tumor mechanisms including apoptosis, proteasome inhibition, mTOR, CDK, and HDAC inhibition.
Main Results:
- Novel agents are broadly classified into immunotherapies (monoclonal antibodies, immunomodulators) and small molecule inhibitors.
- These agents target critical pathways involved in tumorigenesis, such as apoptosis, proteasomes, mTOR, CDKs, and HDACs.
- Various treatment approaches utilizing these novel agents are currently in clinical evaluation for NHL.
Conclusions:
- Emerging novel agents show promise for the treatment of non-Hodgkin lymphoma.
- Targeted therapies and immunotherapies represent a significant advancement in NHL treatment strategies.
- Ongoing clinical evaluations are crucial for establishing the efficacy and safety of these new treatments.
Related Concept Videos
Treatment Resistent Cancers
Treatment Resistant Cancers
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Targeted Cancer Therapies
There are several types of targeted therapies against specific...
Cancer Vaccines
Cancer vaccines come in two categories: preventive (prophylactic) and treatment (active). Preventive vaccines, such as the Human Papillomavirus (HPV) vaccine, protect against viruses that cause certain...
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...

