Suppr超能文献

[89Zr]Zr-DFO-girentuximab 的 PET/CT 成像评估:日本肾细胞癌患者的 1 期临床研究(Zirdac-JP)。

Evaluation of PET/CT imaging with [89Zr]Zr-DFO-girentuximab: a phase 1 clinical study in Japanese patients with renal cell carcinoma (Zirdac-JP).

机构信息

Department of Urology, Yokohama City University, Yokohama City, Kanagawa 236-0004, Japan.

Department of Urology, Kanagawa Cancer Center, Yokohama City, Kanagawa 241-8515, Japan.

出版信息

Jpn J Clin Oncol. 2024 Aug 14;54(8):873-879. doi: 10.1093/jjco/hyae075.

Abstract

BACKGROUND

PET/CT imaging with Zirconium-89 labeled [89Zr]Zr-DFO-girentuximab, which targets tumor antigen CAIX, may aid in the differentiation and characterization of clear cell renal cell carcinomas (RCC) and other renal and extrarenal lesions, and has been studied in European and American cohorts. We report results from a phase I study that evaluated the safety profile, biodistribution, and dosimetry of [89Zr]Zr-DFO-girentuximab in Japanese patients with suspected RCC.

METHODS

Eligible adult patients received 37 MBq (± 10%; 10 mg mass dose) of intravenous [89Zr]Zr-DFO-girentuximab. Safety and tolerability profile was assessed based on adverse events, concomitant medications, physical examination, vital signs, hematology, serum chemistry, urinalysis, human anti-chimeric antibody measurement, and 12-lead electrocardiograms at predefined intervals. Biodistribution and normal organ and tumor dosimetry were evaluated with PET/CT images acquired at 0.5, 4, 24, 72 h and Day 5 ± 2 d after administration.

RESULTS

[89Zr]Zr-DFO-girentuximab was administered in six patients as per protocol. No treatment-emergent adverse events were reported. Dosimetry analysis showed that radioactivity was widely distributed in the body, and that the absorbed dose in healthy organs was highest in the liver (mean ± standard deviation) (1.365 ± 0.245 mGy/MBq), kidney (1.126 ± 0.190 mGy/MBq), heart wall (1.096 ± 0.232 mGy/MBq), and spleen (1.072 ± 0.466 mGy/MBq). The mean effective dose, adjusted by the radioactive dose administered, was 0.470 mSv/MBq. The radiation dose was highly accumulated in the targeted tumor, while any abnormal accumulation in other organs was not reported.

CONCLUSIONS

This study demonstrates that [89Zr]Zr-DFO-girentuximab administered to Japanese patients with suspected RCC has a favorable safety profile and is well tolerated and has a similar dosimetry profile to previously studied populations.

摘要

背景

使用放射性核素标记[89Zr]Zr-DFO-吉妥珠单抗(靶向肿瘤抗原 CAIX)的 PET/CT 成像可辅助鉴别和特征化透明细胞肾细胞癌(RCC)及其他肾内和肾外病变,这在欧美队列中已有研究。我们报告了一项 I 期研究的结果,该研究评估了疑似 RCC 的日本患者中[89Zr]Zr-DFO-吉妥珠单抗的安全性特征、生物分布和剂量学。

方法

符合条件的成年患者接受静脉内 37MBq(±10%;10mg 质量剂量)[89Zr]Zr-DFO-吉妥珠单抗。根据不良事件、伴随用药、体格检查、生命体征、血液学、血清化学、尿液分析、人抗嵌合抗体测量和 12 导联心电图在规定间隔进行安全性和耐受性评估。使用 0.5、4、24、72 小时和给药后 5±2 天的 PET/CT 图像评估生物分布和正常器官及肿瘤剂量学。

结果

按照方案在 6 名患者中给予[89Zr]Zr-DFO-吉妥珠单抗。未报告治疗出现的不良事件。剂量学分析表明,放射性在体内广泛分布,健康器官的吸收剂量以肝脏最高(平均值±标准差)(1.365±0.245mGy/MBq)、肾脏(1.126±0.190mGy/MBq)、心脏壁(1.096±0.232mGy/MBq)和脾脏(1.072±0.466mGy/MBq)。通过给予的放射性剂量调整的平均有效剂量为 0.470mSv/MBq。目标肿瘤中高度积聚了辐射剂量,而未报告其他器官的任何异常积聚。

结论

本研究表明,在疑似 RCC 的日本患者中给予[89Zr]Zr-DFO-吉妥珠单抗具有良好的安全性特征,且耐受良好,其剂量学特征与先前研究的人群相似。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abff/11322881/9d6c052e1e44/hyae075f1.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验