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Immunotherapies for Breast Cancer: From Checkpoint Inhibition to Emerging Cellular Therapies
Ismini Tsagkaraki1, Isaac Gannon2, Alexandros Rampotas2,3
1Oncology Department, Royal Berkshire NHS Foundation Trust, Reading RG1 5AN, UK.
Immunotherapy, particularly immune checkpoint inhibitors (ICIs), shows promise for triple-negative breast cancer (TNBC). Emerging cellular therapies like CAR T-cells offer new strategies to overcome resistance and improve outcomes in breast cancer treatment.
Area of Science:
- Oncology
- Immunology
- Cancer Research
Background:
- Breast cancer subtypes exhibit unique biology influencing therapeutic response.
- Immunotherapy, especially immune checkpoint inhibitors (ICIs), has shown success in triple-negative breast cancer (TNBC).
- Resistance to ICIs is common due to low tumor immunogenicity and immunosuppressive microenvironments.
Purpose of the Study:
- To review current clinical evidence for immunotherapies in breast cancer.
- To highlight emerging cellular immunotherapy strategies.
- To discuss challenges and future directions in breast cancer immunotherapy.
Main Methods:
- Review of current clinical evidence for immunotherapies in breast cancer.
- Summary of emerging cellular immunotherapy strategies (CAR T-cell, TIL, TCR, CAR-NK).
- Discussion of key challenges: antigen specificity, toxicity, and resistance.
Main Results:
- ICIs combined with chemotherapy are a standard of care for TNBC in early and metastatic settings.
- Cellular immunotherapies targeting antigens like HER2, ROR1, MUC1, mesothelin, and B7-H3 are in early clinical evaluation.
- Various cellular approaches aim to overcome antigen presentation barriers and immune evasion.
Conclusions:
- Cellular immunotherapy represents a potential next frontier for breast cancer treatment.
- Overcoming resistance requires addressing antigen specificity, off-tumor toxicity, and the tumor microenvironment.
- Future progress depends on combination approaches and next-generation engineered immune cells for durable, personalized benefit.
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