Novel immunotherapies for breast cancer: Focus on 2023 findings

Int Immunopharmacol. 2024 Feb 15:128:111549. doi: 10.1016/j.intimp.2024.111549. Epub 2024 Jan 23.

Abstract

Immunotherapy has emerged as a revolutionary approach in cancer therapy, and recent advancements hold significant promise for breast cancer (BCa) management. Employing the patient's immune system to combat BCa has become a focal point in immunotherapeutic investigations. Strategies such as immune checkpoint inhibitors (ICIs), adoptive cell transfer (ACT), and targeting the tumor microenvironment (TME) have disclosed encouraging clinical outcomes. ICIs, particularly programmed cell death protein 1 (PD-1)/PD-L1 inhibitors, exhibit efficacy in specific BCa subtypes, including triple-negative BCa (TNBC) and human epidermal growth factor receptor 2 (HER2)-positive cancers. ACT approaches, including tumor-infiltrating lymphocytes (TILs) and chimeric antigen receptor (CAR) T-cell therapy, showed promising clinical outcomes in enhancing tumor recognition and elimination. Targeting the TME through immune agonists and oncolytic viruses signifies a burgeoning field of research. While challenges persist in patient selection, resistance mechanisms, and combination therapy optimization, these novel immunotherapies hold transformative potential for BCa treatment. Continued research and clinical trials are imperative to refine and implement these innovative approaches, paving the way for improved outcomes and revolutionizing the management of BCa. This review provides a concise overview of the latest immunotherapies (2023 studies) in BCa, highlighting their potential and current status.

Keywords: Breast cancer; Clinical trials; Combination therapy; Immunotherapy; Treatment.

Publication types

  • Review

MeSH terms

  • B7-H1 Antigen / metabolism
  • Combined Modality Therapy
  • Humans
  • Immune Checkpoint Inhibitors / therapeutic use
  • Immunotherapy
  • Immunotherapy, Adoptive
  • Lymphocytes, Tumor-Infiltrating
  • Triple Negative Breast Neoplasms* / pathology
  • Tumor Microenvironment

Substances

  • Immune Checkpoint Inhibitors
  • B7-H1 Antigen