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Updated: May 12, 2026

Flow Cytometry-based Assay for the Monitoring of NK Cell Functions
Published on: October 30, 2016
The current status and future impact of targeted therapies in non-Hodgkin lymphoma
Chaitra Ujjani1, Bruce D Cheson
1Georgetown University, 3800 Reservoir Rd. NW, Washington, DC 20007, USA. csu@georgetown.edu
Abstract:
A number of new, biologic targeted therapies have been developed for the treatment of lymphoid malignancies. These include anti-CD20 monoclonal antibodies designed with greater binding affinities and different mechanisms of action profiles compared with rituximab. Other extracellular antigens on B cells and T cells are also being targeted. Monoclonal antibodies have been conjugated to radioisotopes and cellular toxins. In addition, several exciting new small-molecule kinase inhibitors are in development that target intracellular pathways that contribute to the pathogenesis of these diseases. Drugs that affect the tumor microenvironment are also under investigation. The advantage of these targeted agents compared with standard chemotherapy is greater tumor specificity, a more favorable toxicity profile, and, when combined with scientific rationale, and in the appropriate setting, perhaps a better long-term outcome.
Insights
New targeted therapies, including advanced monoclonal antibodies and kinase inhibitors, offer improved specificity and safety for treating lymphoid malignancies compared to traditional chemotherapy.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Biologic targeted therapies represent a significant advancement in treating lymphoid malignancies.
- Existing treatments like rituximab have paved the way for newer agents with improved characteristics.
Purpose of the Study:
- To review novel biologic targeted therapies for lymphoid malignancies.
- To highlight advancements in monoclonal antibodies and small-molecule kinase inhibitors.
- To discuss agents targeting the tumor microenvironment.
Main Methods:
- Review of emerging targeted therapies for lymphoid cancers.
- Analysis of novel monoclonal antibodies targeting extracellular antigens (e.g., CD20).
- Examination of small-molecule kinase inhibitors targeting intracellular pathways.
Main Results:
- New anti-CD20 monoclonal antibodies exhibit enhanced binding and varied mechanisms.
- Antibodies are being conjugated with radioisotopes and toxins for targeted delivery.
- Small-molecule kinase inhibitors show promise in targeting disease pathogenesis.
- Therapies modulating the tumor microenvironment are under investigation.
Conclusions:
- Targeted agents offer greater tumor specificity and a better toxicity profile than standard chemotherapy.
- These novel therapies hold potential for improved long-term outcomes in lymphoid malignancies.
- Further research and appropriate clinical settings are crucial for optimizing their use.
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