Adjuvant and Neoadjuvant Treatment of Triple-Negative Breast Cancer With Chemotherapy

Antonio Marra1, Giuseppe Curigliano

  • 1From the Division of Early Drug Development for Innovative Therapies, European Institute of Oncology (IEO) IRCCS; and Department of Oncology and Haemato-Oncology, University of Milano, Milan, Italy.

Insights

Triple-negative breast cancer (TNBC) is aggressive but chemotherapy-sensitive. Current neoadjuvant chemotherapy (NACT) is standard, but optimal regimens and residual disease treatment require further research for personalized TNBC therapy.

Area of Science:

  • Oncology
  • Genomics
  • Translational Medicine

Background:

  • Triple-negative breast cancer (TNBC) comprises 15-20% of invasive breast carcinomas and lacks ER, PR, and HER2 expression.
  • TNBC exhibits high recurrence rates and poorer survival but shows greater sensitivity to chemotherapy compared to other subtypes.
  • Chemotherapy remains the primary treatment modality for TNBC, despite extensive genomic characterization efforts.

Purpose of the Study:

  • To review current evidence guiding neoadjuvant and adjuvant chemotherapy in early-stage TNBC.
  • To discuss ongoing controversies regarding neoadjuvant chemotherapy regimens, including platinum incorporation and treatment of residual disease.
  • To outline future directions for personalized treatment strategies in early-stage TNBC.

Main Methods:

  • Review of current clinical evidence and treatment guidelines for early-stage TNBC.
  • Discussion of controversies in neoadjuvant chemotherapy (NACT) protocols.
  • Exploration of emerging technologies for personalized treatment approaches.

Main Results:

  • Sequential anthracycline- and taxane-based NACT is the standard for early-stage TNBC, with pathological complete response correlating with survival.
  • Debates persist regarding optimal NACT regimens and the role of chemotherapy in managing residual disease post-NACT.
  • Multi-omics, liquid biopsy, and machine learning show promise for tailoring anticancer therapies.

Conclusions:

  • Chemotherapy is central to early-stage TNBC management, with NACT being the standard approach.
  • Further research is needed to optimize NACT and define the best strategies for patients with residual disease.
  • Integrating advanced technologies like multi-omics and machine learning is crucial for advancing personalized TNBC treatment.

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