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Updated: Dec 20, 2025

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
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.
Abstract:
Triple negative breast cancer (TNBC) is an aggressive breast cancer with historically poor outcomes, primarily due to the lack of effective targeted therapies. The tumor molecular heterogeneity of TNBC has been well recognized, yet molecular subtype driven therapy remains lacking. While neoadjuvant anthracycline and taxane-based chemotherapy remains the standard of care for early stage TNBC, the optimal chemotherapy regimen is debatable. The addition of carboplatin to anthracycline, cyclophosphamide, and taxane (ACT) regimen is associated with improved complete pathologic response (pCR). Immune checkpoint inhibitor (ICI) combinations significantly increase pCR in TNBC. Increased tumor infiltrating lymphocyte (TILs) or the presence of DNA repair deficiency (DRD) mutation is associated with increased pCR. Other targets, such as poly-ADP-ribosyl polymerase inhibitors (PARPi) and Phosphatidylinositol-3-kinase/Protein Kinase B/mammalian target of rapamycin (PI3K-AKT-mTOR) pathway inhibitors, are being evaluated in the neoadjuvant setting. This review examines recent progress in neoadjuvant therapy of TNBC, including platinum, ICI, PARPi, phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha (PIK3CA) pathway targeted therapies, and novel tumor microenvironment (TME) targeted therapy, in addition to biomarkers for the prediction of pCR.
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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