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Updated: Feb 14, 2026

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
[PD-L1 expression and PD-1/PD-L1 inhibitors in breast cancer]
Audrey Monneur1, Anthony Gonçalves2, François Bertucci2
1Institut Paoli-Calmettes, département d'oncologie médicale, 232, boulevard de Sainte-Marguerite, 13009 Marseille, France.
Abstract:
The development of immune checkpoints inhibitors represents one of the major recent advances in oncology. Monoclonal antibodies directed against the programmed cell death protein 1 (PD-1) or its ligand (PD-L1) provides durable disease control, particularly in melanoma, lung, kidney, bladder and head and neck cancers. The purpose of this review is to synthesize current data on the expression of PD-L1 in breast cancer and on the preliminary clinical results of PD-1/PD-L1 inhibitors in breast cancer patients. In breast cancer, PD-L1 expression is heterogeneous and is generally associated with the presence of tumor-infiltrating lymphocytes as well as the presence of poor-prognosis factors, such as young age, high grade, ER-negativity, PR-negativity, and HER-2 overexpression, high proliferative index, and aggressive molecular subtypes (triple negative, basal-like, HER-2-overexpressing). Its prognostic value remains controversial when assessed with immunohistochemistry, whereas it seems favorable in triple-negative cancers when assessed at the mRNA level. Early clinical trials with PD-1/PD-L1 inhibitors in breast cancer have shown efficacy in terms of tumor response and/or disease control in refractory metastatic breast cancers, notably in the triple-negative subtype. Many trials are currently underway, both in the metastatic and neo-adjuvant setting. A crucial issue is identification of biomarkers predictive of response to PD-1/PD-L1 inhibitors.
Insights
Immune checkpoint inhibitors targeting programmed cell death protein 1 (PD-1) and its ligand (PD-L1) show promise in treating breast cancer, especially triple-negative subtypes. Further research is needed to identify biomarkers for predicting treatment response.
Area of Science:
- Oncology
- Immunotherapy
- Cancer Research
Background:
- Immune checkpoint inhibitors (ICIs) targeting PD-1/PD-L1 have revolutionized cancer treatment.
- Their efficacy is well-established in various solid tumors, including melanoma and lung cancer.
- Breast cancer represents a critical area for exploring ICI applications.
Purpose of the Study:
- To review current data on PD-L1 expression in breast cancer.
- To synthesize preliminary clinical outcomes of PD-1/PD-L1 inhibitors in breast cancer patients.
- To highlight the association between PD-L1 expression and breast cancer characteristics.
Main Methods:
- Literature review of studies on PD-L1 expression in breast cancer.
- Analysis of preliminary clinical trial data for PD-1/PD-L1 inhibitors in breast cancer.
- Synthesis of information on prognostic and predictive factors.
Main Results:
- PD-L1 expression in breast cancer is heterogeneous and linked to poor prognostic factors and aggressive subtypes.
- Prognostic value of PD-L1 is controversial via immunohistochemistry but potentially favorable in triple-negative cancers at the mRNA level.
- Early trials show efficacy of PD-1/PD-L1 inhibitors in refractory metastatic breast cancer, particularly triple-negative subtype.
Conclusions:
- PD-1/PD-L1 inhibitors demonstrate preliminary efficacy in metastatic breast cancer, especially triple-negative.
- Ongoing trials are evaluating ICIs in both metastatic and neoadjuvant settings.
- Identifying predictive biomarkers for ICI response is crucial for optimizing breast cancer treatment.
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