Experiences from Introducing Standardized High Dose 131I-mIBG Treatment of Children with Refractory Neuroblastoma: Differences in Effective Dose to Patients and Exposure to Caregivers

Trine Hjørnevik, A. C. Martinsen, S. E. Hagve, Merethe Wigen Andersen, A. Mørk, J. Fjeld, E. Ruud
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引用次数: 5

Abstract

Aims: High dose 131I-meta iodobenzylguanidine (131I-mIBG) combined with radiosensitizing topotecan and peripheral blood stem cell support is a promising treatment regimen for children with neuroblastoma (NB). Here we present our first experiences, with particular focus on in vivo whole-body dosimetry and radiation exposure to family caregivers and hospital staff. Methods: Five children with relapsed or refractory NB were treated during 2012-2014. 131I-mIBG was administered in two fractions at two weeks apart, aiming for a total whole-body radiation-absorbed dose of 4 Gy. The 131I-mIBG activity for the 2nd administration was calculated on the basis of the measured whole-body dose following the 1st administration. Patients were isolated in a lead-shielded room, and all caregivers and staff received radiation safety training, and carried an electronic personal dosimeter. Results: The total administered activity ranged from 5.1 to 28.6 GBq (median: 22.9 GBq), resulting in effective whole-body doses ranging from 2.1 to 4.3 Gy (median: 3.8 Gy). Two out of five patients deviated from the anticipated dose exposure defined by the treatment protocol; one patient received 4.3 Gy after a single administration, and for one patient the total whole-body dose was lower than anticipated (2.1 Gy). Radiation dose to family caregivers ranged from 0.1 to 8.0 mSv. For staff members, the overall radiation dose was low, and provided no concern regarding personal dosimetry. Conclusion: High-dose 131I-mIBG treatment of children with NB has been successfully established at our institution. Radiation doses to caregivers and hospital staff are acceptable and in compliance with national and international guidelines. Two out of five patients deviated from the anticipated dose exposure, hence, accurate dosimetry-guidance during administration of high dose 131I-mIBG treatment is necessary.
引入标准高剂量131I-mIBG治疗难治性神经母细胞瘤儿童的经验:患者有效剂量和护理人员暴露的差异
目的:大剂量碘化碘苄基胍(131I-mIBG)联合放射增敏拓扑替康和外周血干细胞支持是治疗儿童神经母细胞瘤(NB)的一种有前景的治疗方案。在这里,我们介绍了我们的第一次经验,特别关注体内全身剂量测定和家庭护理人员和医院工作人员的辐射暴露。方法:选取2012-2014年收治的5例复发或难治性NB患儿。131I-mIBG分两部分给药,间隔两周,目标是全身总辐射吸收剂量为4gy。第二次给药的131I-mIBG活性是根据第一次给药后测量的全身剂量计算的。患者被隔离在一个铅屏蔽的房间里,所有护理人员和工作人员都接受了辐射安全培训,并携带了电子个人剂量计。结果:总给药活性范围为5.1至28.6 GBq(中位数:22.9 GBq),导致全身有效剂量范围为2.1至4.3 Gy(中位数:3.8 Gy)。五分之二的患者偏离了治疗方案规定的预期剂量暴露;1例患者单次给药后接受4.3 Gy, 1例患者全身总剂量低于预期(2.1 Gy)。对家庭照顾者的辐射剂量为0.1至8.0毫西弗。对工作人员来说,总的辐射剂量很低,不涉及个人剂量测定。结论:我院已成功建立了高剂量131I-mIBG治疗小儿NB的方法。对护理人员和医院工作人员的辐射剂量是可以接受的,符合国家和国际准则。五分之二的患者偏离了预期的剂量暴露,因此,在给予高剂量131I-mIBG治疗期间,精确的剂量学指导是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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