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

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Authors: Joni J. Nijveldt, Siri af Burén, Thuy A. Tran, Emma Jussing, Joachim N. Nilsson, Anna Kistner, Rimma Axelsson, J Bergh, Johan Hartman, Antonios Tzortzakakis, Renske Altena
Cited by: 1
References: 11

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 [89Zr]Zr-atezolizumab could more accurately identify patients with mTNBC who may benefit from immune checkpoint inhibitor therapy. Methods: Three patients with mTNBC underwent [89Zr]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. Results: 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. Conclusion: A work-up with [89Zr]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.

Fields of Study & Subjects

Cancer Immunotherapy and Biomarkers Radiopharmaceutical Chemistry and Applications Immunotherapy and Immune Responses

Publication details

Journal / source
Journal of Nuclear Medicine
Publisher
Society of Nuclear Medicine
Volume
67
Issue
5
Pages
681–686
Publication date
29 January 2026
Language
EN