Phase I Study of [68Ga]Ga-Anti-CD206-sdAb for PET/CT Assessment of Protumorigenic Macrophage Presence in Solid Tumors (MMR Phase I).

IF 9.1 1区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Journal of Nuclear Medicine Pub Date : 2023-09-01 Epub Date: 2023-07-20 DOI:10.2967/jnumed.122.264853
Odrade Gondry, Catarina Xavier, Laurens Raes, Johannes Heemskerk, Nick Devoogdt, Hendrik Everaert, Karine Breckpot, Quentin Lecocq, Lore Decoster, Christel Fontaine, Denis Schallier, Sandrine Aspeslagh, Ilse Vaneycken, Geert Raes, Jo A Van Ginderachter, Tony Lahoutte, Vicky Caveliers, Marleen Keyaerts
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Abstract

Macrophages play an important role throughout the body. Antiinflammatory macrophages expressing the macrophage mannose receptor (MMR, CD206) are involved in disease development, ranging from oncology to atherosclerosis and rheumatoid arthritis. [68Ga]Ga-NOTA-anti-CD206 single-domain antibody (sdAb) is a PET tracer targeting CD206. This first-in-human study, as its primary objective, evaluated the safety, biodistribution, and dosimetry of this tracer. The secondary objective was to assess its tumor uptake. Methods: Seven patients with a solid tumor of at least 10 mm, an Eastern Cooperative Oncology Group score of 0 or 1, and good renal and hepatic function were included. Safety was evaluated using clinical examination and blood sampling before and after injection. For biodistribution and dosimetry, PET/CT was performed at 11, 90, and 150 min after injection; organs showing tracer uptake were delineated, and dosimetry was evaluated. Blood samples were obtained at selected time points for blood clearance. Metabolites in blood and urine were assessed. Results: Seven patients were injected with, on average, 191 MBq of [68Ga]Ga-NOTA-anti-CD206-sdAb. Only 1 transient adverse event of mild severity was considered to be possibly, although unlikely, related to the study drug (headache, Common Terminology Criteria for Adverse Events grade 1). The blood clearance was fast, with less than 20% of the injected activity remaining after 80 min. There was uptake in the liver, kidneys, spleen, adrenals, and red bone marrow. The average effective dose from the radiopharmaceutical was 4.2 mSv for males and 5.2 mSv for females. No metabolites were detected. Preliminary data of tumor uptake in cancer lesions showed higher uptake in the 3 patients who subsequently progressed than in the 3 patients without progression. One patient could not be evaluated because of technical failure. Conclusion: [68Ga]Ga-NOTA-anti-CD206-sdAb is safe and well tolerated. It shows rapid blood clearance and renal excretion, enabling high contrast-to-noise imaging at 90 min after injection. The radiation dose is comparable to that of routinely used PET tracers. These findings and the preliminary results in cancer patients warrant further investigation of this tracer in phase II clinical trials.

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[68Ga]Ga-Anti-CD206-sdAb用于 PET/CT 评估实体瘤原发巨噬细胞存在的 I 期研究(MMR I 期)。
巨噬细胞在全身发挥着重要作用。表达巨噬细胞甘露糖受体(MMR,CD206)的抗炎巨噬细胞参与了从肿瘤到动脉粥样硬化和类风湿性关节炎等各种疾病的发展。[68Ga]Ga-NOTA-anti-CD206 单域抗体(sdAb)是一种靶向 CD206 的 PET 示踪剂。这项首次人体研究的主要目的是评估这种示踪剂的安全性、生物分布和剂量学。次要目标是评估其肿瘤摄取情况。研究方法研究对象包括七名实体瘤至少为 10 毫米、东部合作肿瘤学组评分为 0 或 1 分、肝肾功能良好的患者。通过注射前后的临床检查和血液采样评估安全性。为了进行生物分布和剂量测定,在注射后 11、90 和 150 分钟进行了 PET/CT;对显示示踪剂摄取的器官进行了划定,并对剂量测定进行了评估。在选定的时间点采集血液样本,用于血液清除。对血液和尿液中的代谢物进行评估。结果七名患者平均注射了 191 MBq 的[68Ga]Ga-NOTA-抗-CD206-sdAb。只有 1 例轻微的一过性不良反应(头痛,不良反应通用术语标准 1 级)被认为可能与研究药物有关,但可能性不大。血液清除速度很快,80 分钟后注射活性的残留量不到 20%。肝脏、肾脏、脾脏、肾上腺和红骨髓均有吸收。放射性药物的平均有效剂量为:男性 4.2 mSv,女性 5.2 mSv。没有检测到代谢物。癌症病灶中肿瘤摄取量的初步数据显示,3 名后来病情恶化的患者的摄取量高于 3 名没有病情恶化的患者。一名患者因技术故障无法进行评估。结论[68Ga]Ga-NOTA-抗-CD206-sdAb安全且耐受性良好。它的血液清除和肾脏排泄速度快,注射后90分钟即可进行高对比度-噪声成像。辐射剂量与常规使用的 PET 示踪剂相当。这些发现以及在癌症患者中的初步结果证明,有必要在第二阶段临床试验中进一步研究这种示踪剂。
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来源期刊
Journal of Nuclear Medicine
Journal of Nuclear Medicine 医学-核医学
CiteScore
13.00
自引率
8.60%
发文量
340
审稿时长
1 months
期刊介绍: The Journal of Nuclear Medicine (JNM), self-published by the Society of Nuclear Medicine and Molecular Imaging (SNMMI), provides readers worldwide with clinical and basic science investigations, continuing education articles, reviews, employment opportunities, and updates on practice and research. In the 2022 Journal Citation Reports (released in June 2023), JNM ranked sixth in impact among 203 medical journals worldwide in the radiology, nuclear medicine, and medical imaging category.
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