Current Status and Advances in Anti-Androgen Therapy for Triple-Negative Breast Cancer

Jing-Bo Li1, Wen-Fei Xia2

  • 1The Second Clinical Medical School of Shandong University, Jinan, 250033, China.

Current Medical Science
|August 25, 2025
PubMed

Insights

Androgen receptor (AR)-positive triple-negative breast cancer (TNBC) shows promise for targeted therapy using AR antagonists. Combination treatments and understanding AR

Area of Science:

  • Oncology
  • Molecular Biology
  • Precision Medicine

Background:

  • Triple-negative breast cancer (TNBC) is heterogeneous, necessitating subtype-specific treatments.
  • Androgen receptor (AR)-positive TNBC is a recognized molecular subtype with therapeutic potential.
  • Current treatments for AR-positive TNBC primarily involve AR antagonists like enobosarm, bicalutamide, and enzalutamide.

Purpose of the Study:

  • To explore the therapeutic potential of AR-targeted therapies in AR-positive TNBC.
  • To investigate combination strategies to enhance the efficacy of anti-AR agents.
  • To elucidate the role of AR signaling in the tumor microenvironment and its interaction with immunotherapy.

Main Methods:

  • Review of existing literature on AR-targeted therapies in TNBC.
  • Analysis of preclinical and clinical studies investigating AR antagonists.
  • Exploration of combination therapy approaches including chemotherapy, immunotherapy, and PARP inhibitors.

Main Results:

  • AR antagonists are primary agents for AR-positive TNBC.
  • Combination therapies integrating anti-AR agents with chemotherapy, immunotherapy, or PARP inhibitors are under investigation.
  • AR signaling influences the tumor microenvironment, suggesting AR inhibition can enhance immune checkpoint inhibitor efficacy.

Conclusions:

  • AR-targeted therapy is a promising strategy for personalized treatment of AR-positive TNBC.
  • Further research is needed to overcome limitations and challenges associated with anti-AR therapies.
  • Combination approaches hold potential for improving treatment outcomes in TNBC.

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