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

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.

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Publication Details

Journal
Journal of Nuclear Medicine
Published
2026-01-29
DOI
https://doi.org/10.2967/jnumed.125.271459
Primary Topic
Cancer Immunotherapy and Biomarkers
Type
article
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article

Feasibility of [ 89 Zr]Zr-Atezolizumab Immuno-PET for PD-L1 Quantification in the Clinical Work-up of Metastatic Triple-Negative Breast Cancer

Antonios Tzortzakakis, Emma Jussing, Anna Kistner, J Bergh et al.
Journal of Nuclear Medicine
Cancer Immunotherapy and Biomarkers
article

Feasibility of [ 89 Zr]Zr-Atezolizumab Immuno-PET for PD-L1 Quantification in the Clinical Work-up of Metastatic Triple-Negative Breast Cancer

Antonios Tzortzakakis, Emma Jussing, Anna Kistner, J Bergh, Siri af Burén, Joachim N. Nilsson, Rimma Axelsson, Joni J. Nijveldt, Johan Hartman, Thuy A. Tran, Renske Altena
article en

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.

Journal of Nuclear Medicine
University Medical Center Groningen (NL), Karolinska University Hospital (SE), Karolinska Institutet (SE), Isala (NL)
Good health and well-being
Openalex Percentile: Top 73%
Cancer Immunotherapy and Biomarkers
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