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Facts and Hopes in Immunotherapy for Early-Stage Triple-Negative Breast Cancer

Journal

CLINICAL CANCER RESEARCH
Volume 29, Issue 13, Pages 2362-2370

Publisher

AMER ASSOC CANCER RESEARCH
DOI: 10.1158/1078-0432.CCR-22-0701

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A significant proportion of early-stage triple-negative breast cancer patients have high levels of tumor-infiltrating lymphocytes, indicating a strong endogenous immune response against cancer. Immune-checkpoint inhibition combined with chemotherapy has become the standard of care for these patients. Future challenges include identifying which patients can be treated with immune-checkpoint inhibition alone or with reduced chemotherapy, determining the optimal duration of treatment, and finding biomarkers for treatment response prediction. For patients who do not respond effectively to current treatment, developing new immunomodulatory therapies and response-guided neoadjuvant approaches are needed.
A substantial fraction of early-stage triple-negative breast cancer (eTNBC) is characterized by high levels of stromal tumor-infiltrating lymphocytes (sTIL) and has a good prognosis even without systemic treatment, highlighting the importance of an endogenous anticancer immune response. Still, a considerable proportion of patients with eTNBC need some therapeutical push to kick-start this immune response. Exploiting this immune response with immune-checkpoint inhibition (ICI), in combination with chemotherapy, has made its way into standard of care in eTNBC. Major challenges in the near future include finding those patients with eTNBC who can be treated with ICI alone or with a reduced chemotherapy backbone. Exploring the optimal duration of ICI and finding biomarkers to predict response will be key to enable personalized implementation of ICI in patients with eTNBC. For patients who currently do not respond effectively to ICI plus chemotherapy, challenges lie in finding new immunomodulatory therapies and developing response-guided neoadjuvant approaches.

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