中国[177Lu]Lu-DOTA-TATE治疗后的辐射照射和防护建议。

IF 3.1 3区 医学 Q1 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING EJNMMI Research Pub Date : 2024-11-28 DOI:10.1186/s13550-024-01185-4
Fei Liu, Panli Li, Junyan Xu, Jianping Zhang, Xiaoping Xu, Zhihao Chen, Ying Qiao, Yun Liang, Jie Chen, Shaoli Song
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引用次数: 0

摘要

背景:我们首次在中国开展了一项关于胃肠胰神经内分泌肿瘤(GEP-NENs)患者接受[177Lu]Lu-DOTA-TATE治疗后辐射暴露的研究,旨在为这方面的辐射防护提供指导和参考。本研究共招募了30名接受[177Lu]Lu-DOTA-TATE治疗的GEP-NENs患者。我们测量了每位患者在注射期间和用药后0-6 h的外剂量率(EDR)值,以及医护人员和周围环境的辐射剂量(RD)值。我们对[177Lu]Lu-DOTA-TATE治疗后不同时间出院的患者进行了双指数曲线拟合,并估算了公众的辐射剂量:30例患者中,有27例患者完成了4个周期的[177Lu]Lu-DOTA-TATE治疗,估算出的对公众的RD表明,对于患者的成年家属、10岁以上儿童、3-10岁儿童和同事,患者可在注射后至少24 h、48 h、144 h和192 h开始日常接触,以确保4次治疗后的总RD值不超标。在接受[177Lu]Lu-DOTA-TATE治疗的患者住院期间,给药护士和病房环境接受的累积剂量均远低于国家RD限值:本研究对接受[177Lu]Lu-DOTA-TATE治疗的GEP-NENs患者的EDR值衰减模式进行了拟合分析,以制定患者出院时间指南,并为患者出院后的公众辐射防护提供建议。试验注册:GEP-NETs 患者使用镥[177Lu]奥曲肽注射液与奥曲肽 LAR 治疗的比较研究,NCT05459844。https://clinicaltrials.gov/study/NCT05459844?cond=NCT05459844&rank=1 。2022 年 7 月 5 日注册。
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Radiation exposure and protection advice after [177Lu]Lu-DOTA-TATE therapy in China.

Background: We conducted a study on radiation exposure in patients with gastroenteropancreatic neuroendocrine neoplasms (GEP-NENs) treated with [177Lu]Lu-DOTA-TATE in China for the first time, aiming to provide guidance and reference for radiation protection in this regard. A total of 30 GEP-NENs patients who received [177Lu]Lu-DOTA-TATE therapy were recruited in the study. We measured the external dose rate (EDR) values of each patient during the injection and 0-6 h post-administration period, as well as the radiation dose (RD) values to healthcare nurses and the surrounding environment. We performed a double exponential curve fitting and estimated the RD to the public from patients discharged at different times after [177Lu]Lu-DOTA-TATE therapy.

Results: Among the 30 patients, 27 patients completed 4 cycles of [177Lu]Lu-DOTA-TATE treatments, the estimated RD to the public indicated that for adult family members, children above 10 years old, children aged 3-10 and coworkers of the patients, patients could begin daily contact at least 24 h, 48 h, 144 h and 192 h after injection to ensure that the total RD values after four treatments not exceed the limit. During the hospitalization of patients receiving [177Lu]Lu-DOTA-TATE, the cumulative dose received by the administering nurses and to the ward environment were both well below the national RD limits.

Conclusions: This study conducted a fitting analysis of the decay pattern of EDR values in GEP-NENs patients undergoing [177Lu]Lu-DOTA-TATE therapy, in order to establish guidelines for patient discharge timing and provide recommendations for radiation protection for the general public after patient discharge. Trial registration A Study Comparing Treatment With Lutetium[177Lu] Oxodotreotide Injection to Octreotide LAR in Patients With GEP-NETs, NCT05459844. https://clinicaltrials.gov/study/NCT05459844?cond=NCT05459844&rank=1 . Registered 5 July 2022.

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来源期刊
EJNMMI Research
EJNMMI Research RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING&nb-
CiteScore
5.90
自引率
3.10%
发文量
72
审稿时长
13 weeks
期刊介绍: EJNMMI Research publishes new basic, translational and clinical research in the field of nuclear medicine and molecular imaging. Regular features include original research articles, rapid communication of preliminary data on innovative research, interesting case reports, editorials, and letters to the editor. Educational articles on basic sciences, fundamental aspects and controversy related to pre-clinical and clinical research or ethical aspects of research are also welcome. Timely reviews provide updates on current applications, issues in imaging research and translational aspects of nuclear medicine and molecular imaging technologies. The main emphasis is placed on the development of targeted imaging with radiopharmaceuticals within the broader context of molecular probes to enhance understanding and characterisation of the complex biological processes underlying disease and to develop, test and guide new treatment modalities, including radionuclide therapy.
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