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Published on: August 23, 2024
Targeted based therapy in nodal T-cell lymphomas
Dai Chihara1, Milos Miljkovic2, Swaminathan P Iyer3
1Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, USA. dchihara@mdanderson.org.
Targeted therapies show promise for T-cell lymphomas (TCL), with brentuximab vedotin and ALK inhibitors effective in specific subtypes. However, monotherapy targeting common genetic alterations offers limited durable responses, necessitating combination treatments for T-cell lymphomas.
Area of Science:
- Oncology
- Hematology
- Molecular Biology
Background:
- T-cell lymphomas (TCL) are diverse neoplasms of mature T lymphocytes.
- Recent biological insights have improved TCL classification, but clinical trials lag.
- Biomarker-driven treatments like brentuximab vedotin and ALK inhibitors show efficacy in specific TCL subtypes.
Purpose of the Study:
- To review the current status and role of targeted therapies in nodal T-cell lymphomas.
- To highlight the potential and limitations of biomarker-driven treatments in TCL.
- To discuss the need for combination therapies in T-cell lymphomagenesis.
Main Methods:
- Literature review of targeted therapies in nodal T-cell lymphomas.
- Analysis of biomarker-driven treatment efficacy and limitations.
- Discussion of ongoing clinical trials for combination therapies.
Main Results:
- Brentuximab vedotin is standard for CD30+ TCL and relapsed/refractory ALCL.
- ALK inhibitors show responses in ALK+ ALCL.
- Monotherapies targeting PI3K/mTOR, JAK/STAT, and epigenetic regulators yield unsatisfactory and non-durable responses.
Conclusions:
- Targeted therapies offer specific treatment avenues in TCL, but monotherapy limitations persist.
- Combination treatments are crucial for addressing the multistep nature of T-cell lymphomagenesis.
- Further research is needed to optimize biology/biomarker-driven strategies in TCL.
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