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Abstract Human epidermal growth factor receptor 2–positive (HER2 + ) breast cancer accounts for ~25% of breast cancer cases. Monoclonal antibodies (mAbs) against HER2 have led to unparalleled clinical benefit for a subset of patients with HER2 + breast cancer. In this narrative review, we summarize advances in the understanding of immune system interactions, examine clinical developments, and suggest rationales for future investigation of immunotherapies for HER2 + breast cancer. Complex interactions have been found between different branches of the immune system, HER2 + breast cancer, and targeted treatments (approved and under investigation). A new wave of immunotherapies, such as novel HER2-directed mAbs, antibody drug conjugates, vaccines, and adoptive T-cell therapies, are being studied in a broad population of patients with HER2-expressing tumors. The development of immunotherapies for HER2 + breast cancer represents an evolving field that should take into account interactions between different components of the immune system.
Costa et al. (Thu,) studied this question.