阿替唑单抗
医学
转移性乳腺癌
肿瘤科
化疗
内科学
乳腺癌
免疫疗法
癌症
CA15-3号
免疫检查点
活检
免疫系统
免疫组织化学
病变
靶向治疗
疾病
作者
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
标识
DOI:10.2967/jnumed.125.271459
摘要
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.
科研通智能强力驱动
Strongly Powered by AbleSci AI