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Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
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Neoantigen-Driven Immunotherapy in Triple-Negative Breast Cancer: Emerging Strategies and Clinical Potential
Peter A Shatalov1, Anna A Bukaeva1, Egor M Veselovsky1
1National Medical Research Radiological Centre of the Ministry of Health of the Russian Federation, 249036 Obninsk, Russia.
Biomedicines
|September 27, 2025
Summary
Neoantigen-based immunotherapies show promise for triple-negative breast cancer (TNBC), an aggressive cancer subtype. Challenges include prediction accuracy and cost, but combinational strategies and TME modification offer future solutions.
Area of Science:
- Oncology
- Immunology
- Genetics
Background:
- Triple-negative breast cancer (TNBC) is an aggressive breast cancer subtype with poor prognosis.
- Current therapies are limited, necessitating novel treatment strategies.
- TNBC's unique immunological features present opportunities for immunotherapy.
Purpose of the Study:
- To review neoantigen-based therapeutic approaches for TNBC.
- To analyze the tumor microenvironment (TME) and its role in therapeutic success.
- To discuss methods for neoantigen identification, prioritization, and therapeutic modalities.
Main Methods:
- Review of current literature on neoantigen-based therapies in TNBC.
- Analysis of tumor microenvironment components and their impact.
- Examination of neoantigen identification technologies and prediction algorithms.
- Discussion of therapeutic modalities including adoptive cell therapies and personalized vaccines.
Main Results:
- TNBC is characterized by patient-specific neoantigens, with TP53 being a recurrently mutated gene.
- The balance of immunoactivating and immunosuppressive cells in the TME is crucial for treatment outcomes.
- Current clinical trials show a gap between proof-of-concept and broad applicability due to prediction inaccuracies, cost, and time.
Conclusions:
- Neoantigen-driven immunotherapies hold significant potential for TNBC treatment.
- Overcoming challenges requires combinational strategies, TME modulation, and optimized production workflows.
- Further research into cost-effective and accurate neoantigen identification is essential.
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