Feasibility of [<sup>89</sup>Zr]Zr-Atezolizumab Immuno-PET for PD-L1 Quantification in the Clinical Work-up of Metastatic Triple-Negative Breast Cancer.
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- Record sourced from PubMed, PMID 41611476.
- Also identified by DOI 10.2967/jnumed.125.271459.
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Abstract
Immune checkpoint inhibitors combined with chemotherapy are established as first-line therapy for patients with programmed death ligand 1 (PD-L1)-positive metastatic triple-negative breast cancer (mTNBC). We evaluated whether immuno-PET using [<sup>89</sup>Zr]Zr-atezolizumab could more accurately identify patients with mTNBC who may benefit from immune checkpoint inhibitor therapy. <b>Methods:</b> Three patients with mTNBC underwent [<sup>89</sup>Zr]Zr-atezolizumab PET/CT followed by a biopsy of a targeted metastatic lesion. Patients received atezolizumab plus chemotherapy if either immunohistochemistry of the metastatic lesion or PET imaging showed PD-L1 positivity. <b>Results:</b> All patients had tracer-avid metastatic lesions on PET. Two of 3 biopsied, tracer-avid lesions were PD-L1 negative on immunohistochemistry. Intraindividual heterogeneity in tracer uptake was noted. All patients were treated with atezolizumab plus chemotherapy, with all demonstrating an initial response. <b>Conclusion:</b> A work-up with [<sup>89</sup>Zr]Zr-atezolizumab immuno-PET is clinically feasible. This molecular imaging-based strategy holds potential as a noninvasive tool to more accurately identify patients with mTNBC who may benefit from immune checkpoint inhibitor therapy.
Medical subject headings
- Antibodies, Monoclonal, Humanized
- B7-H1 Antigen
- Triple Negative Breast Neoplasms
- Positron Emission Tomography Computed Tomography
- Immune Checkpoint Inhibitors
- Molecular Imaging