Department of Medical Oncology, Amsterdam UMC location Vrije Universiteit Amsterdam, De Boelelaan 1117, 1081 HV, Amsterdam, the Netherlands.
Imaging and Biomarkers, Cancer Center Amsterdam, De Boelelaan 1117, 1081 HV, Amsterdam, the Netherlands.
Eur J Nucl Med Mol Imaging. 2023 Jun;50(7):2068-2080. doi: 10.1007/s00259-023-06164-w. Epub 2023 Mar 2.
Although lymphocyte activation gene-3 (LAG-3) directed therapies demonstrate promising clinical anti-cancer activity, only a subset of patients seems to benefit and predictive biomarkers are lacking. Here, we explored the potential use of the anti-LAG-3 antibody tracer [Zr]Zr-BI 754111 as a predictive imaging biomarker and investigated its target specific uptake as well as the correlation of its tumor uptake and the tumor immune infiltration.
Patients with head and neck (N = 2) or lung cancer (N = 4) were included in an imaging substudy of a phase 1 trial with BI 754091 (anti-PD-1) and BI 754111 (anti-LAG-3). After baseline tumor biopsy and [F]FDG-PET, patients were given 240 mg of BI 754091, followed 8 days later by administration of [Zr]Zr-BI 754111 (37 MBq, 4 mg). PET scans were performed 2 h, 96 h, and 144 h post-injection. To investigate target specificity, a second tracer administration was given two weeks later, this time with pre-administration of 40 (N = 3) or 600 mg (N = 3) unlabeled BI 754111, followed by PET scans at 96 h and 144 h post-injection. Tumor immune cell infiltration was assessed by immunohistochemistry and RNA sequencing.
Tracer uptake in tumors was clearly visible at the 4-mg mass dose (tumor-to-plasma ratio 1.63 [IQR 0.37-2.89]) and could be saturated by increasing mass doses (44 mg: 0.67 [IQR 0.50-0.85]; 604 mg: 0.56 [IQR 0.42-0.75]), demonstrating target specificity. Tumor uptake correlated to immune cell-derived RNA signatures.
[Zr]Zr-BI-754111 PET imaging shows favorable technical and biological characteristics for developing a potential predictive imaging biomarker for LAG-3-directed therapies.
ClinicalTrials.gov , NCT03780725. Registered 19 December 2018.
尽管淋巴细胞激活基因 3(LAG-3)导向疗法显示出有前景的临床抗癌活性,但似乎只有一部分患者从中受益,并且缺乏预测性生物标志物。在这里,我们探讨了使用抗 LAG-3 抗体示踪剂 [Zr]Zr-BI 754111 作为预测性成像生物标志物的潜力,并研究了其靶特异性摄取以及其肿瘤摄取与肿瘤免疫浸润的相关性。
2 名头颈部(N=2)或肺癌(N=4)患者入组了一项 1 期试验的影像学子研究,该试验使用 BI 754091(抗 PD-1)和 BI 754111(抗 LAG-3)。在基线肿瘤活检和 [F]FDG-PET 后,患者给予 240mg BI 754091,8 天后给予 [Zr]Zr-BI 754111(37MBq,4mg)。注射后 2h、96h 和 144h 进行 PET 扫描。为了研究靶特异性,两周后再次给予第二种示踪剂,此次给药前给予 40mg(N=3)或 600mg(N=3)未标记的 BI 754111,然后在注射后 96h 和 144h 进行 PET 扫描。通过免疫组织化学和 RNA 测序评估肿瘤免疫细胞浸润。
在 4mg 质量剂量时,肿瘤中的示踪剂摄取清晰可见(肿瘤与血浆比 1.63[IQR 0.37-2.89]),并且可以通过增加质量剂量来饱和(44mg:0.67[IQR 0.50-0.85];604mg:0.56[IQR 0.42-0.75]),证明了靶特异性。肿瘤摄取与免疫细胞衍生的 RNA 特征相关。
[Zr]Zr-BI-754111 PET 成像显示出良好的技术和生物学特性,有望开发出用于 LAG-3 导向治疗的潜在预测性成像生物标志物。
ClinicalTrials.gov,NCT03780725。2018 年 12 月 19 日注册。