Neoadjuvant Treatment for Triple Negative Breast Cancer: Recent Progresses and Challenges

Jin Sun Lee1, Susan E Yost1, Yuan Yuan1

  • 1Department of Medical Oncology & Molecular Therapeutics, City of Hope Comprehensive Cancer Center and Beckman Research Institute, Duarte, CA 91010, USA.

Cancers
|June 4, 2020
PubMed

Insights

Neoadjuvant therapies for triple-negative breast cancer (TNBC) are advancing, with carboplatin and immune checkpoint inhibitors showing promise. Biomarkers like tumor-infiltrating lymphocytes and DNA repair deficiency aid in predicting treatment response.

Area of Science:

  • Oncology
  • Medical Research

Background:

  • Triple-negative breast cancer (TNBC) is aggressive with limited targeted therapies.
  • Tumor heterogeneity in TNBC necessitates subtype-specific treatment strategies.
  • Neoadjuvant chemotherapy is standard, but optimal regimens and novel approaches are under investigation.

Purpose of the Study:

  • To review recent advancements in neoadjuvant therapies for TNBC.
  • To explore the efficacy of various targeted agents and biomarkers.
  • To highlight progress in predicting treatment outcomes.

Main Methods:

  • Review of current literature on neoadjuvant treatments for TNBC.
  • Analysis of studies involving platinum-based chemotherapy, immune checkpoint inhibitors (ICIs), PARP inhibitors (PARPi), and PI3K-AKT-mTOR pathway inhibitors.
  • Examination of biomarkers associated with complete pathologic response (pCR).

Main Results:

  • Carboplatin addition to ACT regimens improves pCR.
  • ICI combinations significantly enhance pCR rates in TNBC.
  • Tumor-infiltrating lymphocytes (TILs) and DNA repair deficiency (DRD) mutations correlate with increased pCR.
  • PARPi and PI3K-AKT-mTOR pathway inhibitors are under evaluation.
  • Novel tumor microenvironment (TME) targeted therapies are emerging.

Conclusions:

  • Neoadjuvant treatment for TNBC is evolving with promising targeted therapies.
  • Biomarkers like TILs and DRD are crucial for predicting pCR.
  • Further research into novel agents and TME-targeted therapies is warranted.

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