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Updated: Feb 2, 2026

Neutrophil Isolation and Analysis to Determine their Role in Lymphoma Cell Sensitivity to Therapeutic Agents
Published on: March 25, 2016
Introduction of novel agents in the treatment of primary CNS lymphoma
Christian Grommes1, Lakshmi Nayak2, Han W Tun3
1Department of Neurology, Memorial Sloan Kettering Cancer Center, New York, New York.
Abstract:
Novel insights into the pathophysiology of primary central nervous system lymphoma (PCNSL) have identified the B-cell receptor and Toll-like receptor pathway as well as immune evasion and suppressed tumor immune microenvironment as a key mechanism in the pathogenesis of PCNSL. Small molecules and novel agents targeting these aberrant pathways have been introduced into clinical trials targeting the recurrent or refractory PCNSL patient population. Agents like the Bruton tyrosine kinase (BTK) inhibitor ibrutinib or immunomodulatory drugs (IMiDs) like pomalidomide and lenalidomide have shown promising high response rates in the salvage setting. Here, we give an overview about the recent, exciting developments in PCNSL and summarize the results of clinical trials using novel agents in the recurrent and refractory salvage setting, which include immune checkpoint inhibitors, IMiDs, as well as BTK, phosphatidylinositol-3 kinase, and mammalian target of rapamycin inhibitors.
Insights
Novel treatments for primary central nervous system lymphoma (PCNSL) target key pathways. Clinical trials show promising response rates for recurrent or refractory PCNSL using novel agents like BTK inhibitors and IMiDs.
Area of Science:
- Oncology
- Immunology
- Neurology
Background:
- Primary central nervous system lymphoma (PCNSL) pathogenesis involves B-cell receptor and Toll-like receptor pathways.
- Immune evasion and a suppressed tumor immune microenvironment are critical in PCNSL development.
Purpose of the Study:
- To provide an overview of recent advancements in PCNSL treatment.
- To summarize clinical trial results for novel agents in recurrent or refractory PCNSL.
Main Methods:
- Review of recent clinical trials and literature on PCNSL.
- Focus on novel agents targeting aberrant pathways in PCNSL.
Main Results:
- Agents like Bruton tyrosine kinase (BTK) inhibitors (e.g., ibrutinib) and immunomodulatory drugs (IMiDs) show high response rates in salvage settings.
- Clinical trials are evaluating immune checkpoint inhibitors, IMiDs, BTK, phosphatidylinositol-3 kinase, and mammalian target of rapamycin inhibitors.
Conclusions:
- Novel agents targeting specific molecular pathways offer promising therapeutic strategies for PCNSL.
- Further research and clinical trials are essential for optimizing treatment for recurrent or refractory PCNSL.
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