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Updated: Aug 23, 2025

Identifying PD-1/PD-L1 Inhibitors with Surface Plasmon Resonance Technology
Published on: May 2, 2025
Recent advances in atezolizumab-based programmed death-ligand 1 (PD-L1) blockade therapy for breast cancer
Ali Ameri1, Bahareh Tavakoli-Far2, Maryam Rostami3
1Student Research Committee, Faculty of Pharmacy, Hormozgan University of Medical Sciences, Bandar Abbas, Iran.
Abstract:
Breast cancer, the most common cancer in women worldwide, is curable in ∼ 70-80 % of patients with early-stage, non-metastatic disorder. However, advanced breast cancer with distant organ metastases is incurable with available therapeutics. Thus, scientists have sought emerging strategies for treating metastatic breast cancers., Immune checkpoint inhibitors (ICIs) have represented a significant development in breast cancer immunotherapy. Now, targeting immune checkpoint molecules (e.g., programmed cell death protein 1 (PD-1) and programmed cell death ligand 1 (PD-L1)) have attracted increasing attention in the context of breast cancer therapy, chiefly triple-negative breast cancer (TNBC). Atezolizumab, a humanized IgG1 monoclonal antibody (mAb), has been designed to interfere with the binding of the PD-L1 ligand to its receptor. Targeting PD-L1 using atezolizumab potentiates T-cell responses to the tumor and consequently boosts tumor responses. The results of the IMpassion130 trial have recently led to the approval of the combination of atezolizumab and nab-paclitaxel to treat unresectable locally advanced or metastatic patients with PD-L1-positive TNBC. Herein, we summarize the clinical efficacy of atezolizumab in treating breast cancer and briefly discuss the possible immune-related adverse events (irAEs).
Insights
Atezolizumab, an immune checkpoint inhibitor, shows promise in treating advanced triple-negative breast cancer (TNBC) by targeting PD-L1. This immunotherapy, combined with chemotherapy, offers a new treatment avenue for metastatic TNBC patients.
Area of Science:
- Oncology
- Immunotherapy
- Pharmacology
Background:
- Breast cancer is a leading cause of cancer death in women, with advanced stages remaining incurable.
- Emerging immunotherapies, including immune checkpoint inhibitors (ICIs), are being investigated for metastatic breast cancer.
- Targeting immune checkpoints like PD-1/PD-L1 is a key strategy, particularly for triple-negative breast cancer (TNBC).
Purpose of the Study:
- To review the clinical efficacy of atezolizumab in breast cancer treatment.
- To discuss the role of atezolizumab in targeting PD-L1 for immunotherapy.
- To summarize the potential immune-related adverse events (irAEs) associated with atezolizumab therapy.
Main Methods:
- Review of clinical trial data, focusing on the IMpassion130 trial.
- Analysis of atezolizumab's mechanism of action as a monoclonal antibody targeting PD-L1.
- Summary of approved treatment combinations involving atezolizumab.
Main Results:
- Atezolizumab, in combination with nab-paclitaxel, is approved for unresectable locally advanced or metastatic PD-L1-positive TNBC.
- Targeting PD-L1 with atezolizumab enhances T-cell responses against tumors.
- The IMpassion130 trial demonstrated significant outcomes leading to this approval.
Conclusions:
- Atezolizumab represents a significant advancement in breast cancer immunotherapy, especially for TNBC.
- The combination therapy offers a new option for patients with advanced, metastatic PD-L1-positive TNBC.
- Further understanding of irAEs is important for managing patients on atezolizumab therapy.
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