Human dose-escalation study of PET imaging CD8+ T-cell infiltration in solid malignancies with [68Ga]Ga -NODAGA-SNA006

IF 7.6 1区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING European Journal of Nuclear Medicine and Molecular Imaging Pub Date : 2024-12-10 DOI:10.1007/s00259-024-06999-x
Yan Wang, Meng Zheng, Jun Zhao, Chao Wang, Shandong Zhao, Yicong Bian, Na Dai, Yushuang Zheng, Shibiao Sang, Linchuan Guo, Chenrong Huang, Hua Zhang, Jiwei Jiang, Chun Xu, Qi Zhao, Jiajun Han, Tao Xu, Songbing Qin, Liyan Miao
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Abstract

Purpose

A noninvasive method for evaluating the infiltration of CD8+ T cells in tumors is urgently needed to monitor the response to immunotherapy. This study investigated the performance of a [68Ga]Ga-NODAGA-SNA006 in positron emission tomography (PET) imaging of CD8+ T cells in patients with solid malignancies.

Methods

This human dose-escalation PET imaging study involved eleven patients (lung cancer, 8; gastric carcinoma, 1; esophageal carcinoma, 2). Approximately 150 MBq of [68Ga]Ga-NODAGA-SNA006 with varying nanobody masses (100 µg, 300 µg, 500 µg, 800 µg) was administered, and PET/computed tomography (CT) scans were performed at 15–30, 60–90 and 120 min postinjection (p.i.). Data regarding biodistribution, pharmacokinetics and radiation dosimetry were evaluated. CD8+ T-cell infiltration in biopsy samples was also measured via immunohistochemistry (IHC) for correlation analysis with the tumor uptake of [68Ga]Ga-NODAGA-SNA006 PET.

Results

[68Ga]Ga-NODAGA-SNA006 was well tolerated by all eleven subjects. The highest radioactive uptake was observed in the spleen, followed by the kidneys and bladder. Liver uptake decreased with increasing nanobody mass. Rapid clearance (t1/2<30 min) of [68Ga]Ga-NODAGA-SNA006 from whole blood and serum was observed. Furthermore, 68Ga uptake in tumors (SUVmean) exhibited a linear relationship with CD8+ T-cell infiltration in biopsy samples (R2 = 0.757, p = 0.011), suggesting that the tumor uptake of [68Ga]Ga-NODAGA-SNA006 may represent the degree of CD8+ T-cell infiltration in the tumor.

Conclusion

The use of [68Ga]Ga-NODAGA-SNA006 is safe, feasible, and well tolerated. [68Ga]Ga-NONAGA-SNA006 PET imaging can accurately detect CD8 expression inside tumors with favorable pharmacokinetics, thus providing a feasible method for noninvasive quantitative assessment of CD8+ T-cell tumor infiltration and monitoring the response to immunotherapy.

Trial Registration

NCT05126927 (19 November 2021, retrospectively registered).

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[68Ga]Ga -NODAGA-SNA006对实体恶性肿瘤中CD8+ t细胞浸润的PET显像剂量递增研究
目的为监测肿瘤对免疫治疗的反应,迫切需要一种无创的方法来评估CD8+ T细胞在肿瘤中的浸润。本研究探讨了a [68Ga]Ga-NODAGA-SNA006在实体恶性肿瘤患者CD8+ T细胞正电子发射断层扫描(PET)成像中的表现。方法这项人体剂量递增PET成像研究纳入了11例患者(肺癌,8例;胃癌1例;注射约150 MBq的[68Ga]Ga-NODAGA-SNA006,纳米体质量(100µg, 300µg, 500µg, 800µg),并在注射后15-30、60-90和120分钟(p.i)进行PET/计算机断层扫描(CT)。评估了有关生物分布、药代动力学和辐射剂量学的数据。通过免疫组织化学(IHC)检测活检样本中CD8+ t细胞的浸润,分析其与肿瘤摄取[68Ga]Ga-NODAGA-SNA006 PET的相关性。结果11名受试者对[68Ga]Ga-NODAGA-SNA006耐受良好。脾脏的放射性摄取最高,其次是肾脏和膀胱。肝脏摄取随着纳米体质量的增加而降低。在全血和血清中观察到[68Ga]Ga-NODAGA-SNA006的快速清除(t1/2<30 min)。此外,肿瘤中68Ga摄取(SUVmean)与活检样本中CD8+ t细胞浸润呈线性关系(R2 = 0.757, p = 0.011),提示[68Ga]Ga-NODAGA-SNA006的肿瘤摄取可能代表肿瘤中CD8+ t细胞浸润的程度。结论使用[68Ga]Ga-NODAGA-SNA006安全、可行、耐受性好。[68Ga]Ga-NONAGA-SNA006 PET成像可准确检测肿瘤内CD8表达,具有良好的药代动力学,为无创定量评估CD8+ t细胞肿瘤浸润及监测免疫治疗反应提供了可行的方法。试验注册号nct05126927(2021年11月19日,回顾性注册)。
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来源期刊
CiteScore
15.60
自引率
9.90%
发文量
392
审稿时长
3 months
期刊介绍: The European Journal of Nuclear Medicine and Molecular Imaging serves as a platform for the exchange of clinical and scientific information within nuclear medicine and related professions. It welcomes international submissions from professionals involved in the functional, metabolic, and molecular investigation of diseases. The journal's coverage spans physics, dosimetry, radiation biology, radiochemistry, and pharmacy, providing high-quality peer review by experts in the field. Known for highly cited and downloaded articles, it ensures global visibility for research work and is part of the EJNMMI journal family.
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