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Updated: Aug 23, 2025

Tumor Engraftment in a Xenograft Mouse Model of Human Mantle Cell Lymphoma
Published on: March 30, 2018
[Aggressive lymphoma (DLBCL, MCL) - what's new?]
Elisabeth Silkenstedt1, Martin Dreyling1
1Medizinische Klinik III, LMU Klinikum, München.
Advances in understanding lymphoma genetics, like TP53 mutations in mantle cell lymphoma (MCL), are driving new targeted and immunotherapy treatments. However, high-risk patients still need better therapeutic strategies for improved survival.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Context:
- Significant progress in understanding lymphoma molecular basis, including genetic alterations like TP53 mutations in MCL.
- Identification of genetic markers with prognostic impact on disease course.
Purpose:
- To summarize recent findings in tumor biology and therapeutic developments for Diffuse Large B-cell Lymphoma (DLBCL) and MCL.
- To highlight the need for optimized, individualized strategies for high-risk lymphoma patients.
Summary:
- Deepened molecular insights facilitate rapid development of targeted and immuno-based therapies.
- New therapies are increasingly used in first-line treatments for DLBCL and MCL, potentially replacing conventional chemotherapy.
- Despite advances, primary refractory disease and early relapses show moderate responses and limited survival.
Impact:
- Potential for individualized, risk-adapted treatment strategies to improve patient care.
- Highlights the unmet need for advanced therapeutic options for refractory and relapsed lymphoma patients.
- Expands the therapeutic landscape for DLBCL and MCL by integrating novel findings in tumor biology.
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