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用90Y-替伊莫单抗治疗的患者肾脏辐射吸收剂量的估计值。

Estimates of radiation-absorbed dose to kidneys in patients treated with 90Y-ibritumomab tiuxetan.

作者信息

Baechler Sébastien, Hobbs Robert F, Prideaux Andrew R, Recordon Mélanie, Bischof-Delaloye Angelika, Sgouros George

机构信息

The Russell H. Morgan Department of Radiology and Radiological Sciences, Johns Hopkins University, School of Medicine, Baltimore, MD, USA.

出版信息

Cancer Biother Radiopharm. 2008 Oct;23(5):633-9. doi: 10.1089/cbr.2008.0506.

DOI:10.1089/cbr.2008.0506
PMID:18999935
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2936951/
Abstract

UNLABELLED

The aim of the present study was to retrospectively estimate the absorbed dose to kidneys in 17 patients treated in clinical practice with 90Y-ibritumomab tiuxetan for non-Hodgkin's lymphoma, using appropriate dosimetric approaches available.

METHODS

The single-view effective point source method, including background subtraction, is used for planar quantification of renal activity. Since the high uptake in the liver affects the activity estimate in the right kidney, the dose to the left kidney serves as a surrogate for the dose to both kidneys. Calculation of absorbed dose is based on the Medical Internal Radiation Dose methodology with adjustment for patient kidney mass.

RESULTS

The median dose to kidneys, based on the left kidney only, is 2.1 mGy/MBq (range, 0.92-4.4), whereas a value of 2.5 mGy/MBq (range, 1.5-4.7) is obtained, considering the activity in both kidneys.

CONCLUSIONS

Irrespective of the method, doses to kidneys obtained in the present study were about 10 times higher than the median dose of 0.22 mGy/MBq (range, 0.00-0.95) were originally reported from the study leading to Food and Drug Administration approval. Our results are in good agreement with kidney-dose estimates recently reported from high-dose myeloablative therapy with 90Y-ibritumomab tiuxetan.

摘要

未标记

本研究的目的是回顾性评估17例在临床实践中接受90Y-替伊莫单抗治疗非霍奇金淋巴瘤患者的肾脏吸收剂量,采用现有的适当剂量测定方法。

方法

单视野有效点源法,包括背景扣除,用于平面定量肾脏活性。由于肝脏的高摄取会影响右肾的活性估计,因此左肾的剂量可作为双肾剂量的替代。吸收剂量的计算基于医学内照射剂量方法,并根据患者肾脏质量进行调整。

结果

仅基于左肾,肾脏的中位剂量为2.1 mGy/MBq(范围为0.92 - 4.4),而考虑双肾活性时,得到的值为2.5 mGy/MBq(范围为1.5 - 4.7)。

结论

无论采用何种方法,本研究中获得的肾脏剂量比导致美国食品药品监督管理局批准的研究最初报告的中位剂量0.22 mGy/MBq(范围为0.00 - 0.95)高约10倍。我们的结果与最近关于90Y-替伊莫单抗高剂量清髓治疗的肾脏剂量估计结果高度一致。

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本文引用的文献

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J Nucl Med. 2007 Nov;48(11):1871-9. doi: 10.2967/jnumed.107.044016.
2
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Cancer Biother Radiopharm. 2007 Feb;22(1):113-20. doi: 10.1089/cbr.2007.302.
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Patient-specific dosimetry of pretargeted radioimmunotherapy using CC49 fusion protein in patients with gastrointestinal malignancies.使用CC49融合蛋白对胃肠道恶性肿瘤患者进行预靶向放射免疫治疗的个体化剂量测定。
J Nucl Med. 2005 Apr;46(4):642-51.
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MIRD pamphlet no. 16: Techniques for quantitative radiopharmaceutical biodistribution data acquisition and analysis for use in human radiation dose estimates.医学内照射剂量(MIRD)第16号手册:用于人体辐射剂量估计的放射性药物定量生物分布数据采集与分析技术
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