评估 PET/CT 成像与[89Zr]Zr-DFO-吉伦妥昔单抗:日本肾细胞癌患者的 1 期临床研究(Zirdac-JP)。

IF 1.9 4区 医学 Q3 ONCOLOGY Japanese journal of clinical oncology Pub Date : 2024-08-14 DOI:10.1093/jjco/hyae075
Noboru Nakaigawa, Hisashi Hasumi, Daisuke Utsunomiya, Keisuke Yoshida, Yoshinobu Ishiwata, Takashi Oka, Colin Hayward, Kazuhide Makiyama
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引用次数: 0

摘要

背景:锆-89标记的[89Zr]Zr-DFO-吉仑妥昔单抗靶向肿瘤抗原CAIX,其PET/CT成像可能有助于透明细胞肾细胞癌(RCC)及其他肾脏和肾外病变的分化和定性。我们报告了一项 I 期研究的结果,该研究评估了[89Zr]Zr-DFO-吉伦妥昔单抗在日本疑似 RCC 患者中的安全性、生物分布和剂量测量:符合条件的成年患者接受 37 MBq(± 10%;10 毫克质量剂量)的静脉注射[89Zr]Zr-DFO-吉仑妥昔单抗。根据不良反应、伴随用药、体格检查、生命体征、血液学、血清化学、尿液分析、人类抗嵌合抗体测定和预定时间间隔的 12 导联心电图,对安全性和耐受性进行评估。用药后0.5、4、24、72小时和第5天(±2天)采集的PET/CT图像对生物分布、正常器官和肿瘤剂量进行评估:结果:[89Zr]Zr-DFO-吉伦妥昔单抗按照方案对六名患者进行了治疗。未报告治疗引发的不良事件。剂量测定分析表明,放射性在体内广泛分布,健康器官的吸收剂量以肝脏(平均值±标准偏差)(1.365±0.245 mGy/MBq)、肾脏(1.126±0.190 mGy/MBq)、心壁(1.096±0.232 mGy/MBq)和脾脏(1.072±0.466 mGy/MBq)最高。经放射性剂量调整后的平均有效剂量为 0.470 mSv/MBq。放射剂量在靶向肿瘤中高度聚集,而在其他器官中的异常聚集未见报道:这项研究表明,对疑似 RCC 的日本患者施用[89Zr]Zr-DFO-吉伦妥昔单抗具有良好的安全性和耐受性,其剂量测量曲线与之前研究的人群相似。
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Evaluation of PET/CT imaging with [89Zr]Zr-DFO-girentuximab: a phase 1 clinical study in Japanese patients with renal cell carcinoma (Zirdac-JP).

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.

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来源期刊
CiteScore
3.70
自引率
8.30%
发文量
177
审稿时长
3-8 weeks
期刊介绍: Japanese Journal of Clinical Oncology is a multidisciplinary journal for clinical oncologists which strives to publish high quality manuscripts addressing medical oncology, clinical trials, radiology, surgery, basic research, and palliative care. The journal aims to contribute to the world"s scientific community with special attention to the area of clinical oncology and the Asian region. JJCO publishes various articles types including: ・Original Articles ・Case Reports ・Clinical Trial Notes ・Cancer Genetics Reports ・Epidemiology Notes ・Technical Notes ・Short Communications ・Letters to the Editors ・Solicited Reviews
期刊最新文献
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