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Updated: May 30, 2026

Studying Triple Negative Breast Cancer Using Orthotopic Breast Cancer Model
Published on: March 20, 2020
Current treatment options in triple negative breast cancer
Eve Rodler1, Larissa Korde, Julie Gralow
1University of Washington, WA, USA. erodler@seattlecca.org
Abstract:
Triple negative breast cancer (TNBC) refers to a subgroup of breast carcinomas that do not express the estrogen receptor, progesterone receptor, or human epidermal growth factor receptor type 2. This heterogeneous group of tumors has significant overlap with both basal-like tumors (defined through gene expression array) and BRCA1 mutation-associated tumors. Due to a lack of well defined clinical targets, chemotherapy is the standard of care treatment for TNBC. When compared with other breast cancer subtypes, TNBC exhibits at least equivalent, or often superior sensitivity to chemotherapy. However, despite this increased chemosensitivity, TNBC has a worse clinical outcome than other breast cancer subtypes. This has led to the investigation of DNA damaging chemotherapy agents, including platinum drugs, angiogenesis inhibitors, poly(ADP-ribose) polymerase inhibitors, novel microtubule inhibitors, and other targeted therapies in an effort to improve the outcome for patients with these high-risk tumors. Treatment decisions for patients with TNBC should be based on the best currently available evidence, which consists mainly of retrospective and prospective subgroup analyses and phase II prospective data. This review summarizes data from select neoadjuvant, adjuvant, and metastatic chemotherapy clinical trials which included analyses of treatment effects and outcomes in TNBC and/or basal-like breast cancer.
Insights
Triple negative breast cancer (TNBC) shows high sensitivity to chemotherapy but has poor outcomes. Research is exploring novel targeted therapies and DNA damaging agents to improve treatment for this aggressive cancer subtype.
Area of Science:
- Oncology
- Genetics
Background:
- Triple negative breast cancer (TNBC) lacks specific molecular targets, making chemotherapy the standard treatment.
- TNBC often overlaps with basal-like and BRCA1-associated tumors, presenting a complex clinical challenge.
- Despite superior chemotherapy sensitivity, TNBC exhibits worse patient outcomes compared to other breast cancer subtypes.
Purpose of the Study:
- To review current evidence on chemotherapy and targeted therapies for TNBC.
- To analyze treatment effects and outcomes in neoadjuvant, adjuvant, and metastatic settings for TNBC.
- To inform treatment decisions for high-risk TNBC patients based on clinical trial data.
Main Methods:
- Review of select neoadjuvant, adjuvant, and metastatic chemotherapy clinical trials.
- Analysis of subgroup data focusing on TNBC and basal-like breast cancer outcomes.
- Synthesis of retrospective and prospective subgroup analyses and Phase II data.
Main Results:
- TNBC demonstrates significant, often superior, sensitivity to chemotherapy compared to other breast cancer subtypes.
- Existing evidence primarily stems from subgroup analyses and Phase II trials.
- Investigational therapies include platinum drugs, angiogenesis inhibitors, PARP inhibitors, and novel microtubule inhibitors.
Conclusions:
- Improved treatment strategies are needed for TNBC due to its aggressive nature and poor prognosis.
- Targeted therapies and DNA damaging agents are under investigation to enhance TNBC treatment efficacy.
- Evidence-based treatment decisions for TNBC should integrate data from various clinical trial settings.
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