Dosimetric Comparison of Different Radionuclides Used in Metastatic Bone Disease Treatment.

IF 1.5 4区 医学 Q3 PHARMACOLOGY & PHARMACY Current radiopharmaceuticals Pub Date : 2023-01-01 DOI:10.2174/1874471015666220806141755
Handan Tanyildizi Kökkülünk
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Abstract

Introduction: This study aimed to determine the critical organ doses in 223Ra, 89Sr, 153Sm, and 32P treatments via dosimetry using the phantoms.

Material and methods: The OpenDose was used to calculate S values (mGy MBq-1s-1) for bone surface, red bone marrow, urinary bladder wall, testes, ovaries, uterus, and kidneys using male (ICRP110AM) and female (ICRP110AF) phantoms. The cortical thoracic spine was modeled as metastasis. Moreover, the absorbed doses were computed via MIRD formalism according to the activities of 3.3, 148, 2220, and 370 MBq for ICRP110AM and 4.015, 148, 2701, and 370 MBq for ICRP110AF in 223Ra, 89Sr, 153Sm, and 32P treatments, respectively.

Results: Whilst the maximum bone surface doses were found as 1.22E+02 and 8.51E+01 mGy at 32P treatment, the minimum bone surface doses were calculated as 8.42E-02 and 8.26E-02 mGy at 223Ra. In terms of the comparison of red bone marrow, urinary bladder wall, and kidney doses, 153Sm and 89Sr treatments showed maximum doses of 2.45E-03, 1.50E-03, 3.23E-07, 5.45E-06, 1.20E-01, 1.49E-01 mGy and the minimum doses with 3.46E-05, 1.99E-05, 6.33E-09, 8.77E-09, 1.19E-04, 1.15E-04 mGy, respectively. The maximum testes and ovaries-uterus doses were found as 6.17E-08, 7.40E-06, 3.46E-07 mGy in 153Sm treatment, and minimum testes and ovaries doses as 1.70E-09, 1.34E-07 mGy in 223Ra. The minimum uterus dose with 7.03E-09 mGy was determined in 89Sr treatment.

Conclusion: It is observed that 223Ra produces low critical organ doses in the treatment of painful bone metastasis. Among the beta-emitting radionuclides, 89Sr stands out by showing optimal dosimetric results.

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不同放射性核素在转移性骨病治疗中的剂量学比较。
本研究旨在通过幻影剂量法测定223Ra、89Sr、153Sm和32P治疗的关键器官剂量。材料与方法:采用OpenDose软件,用男性(ICRP110AM)和女性(ICRP110AF)模型计算骨表面、红骨髓、膀胱壁、睾丸、卵巢、子宫和肾脏的S值(mGy MBq-1s-1)。胸椎皮质骨模型为转移瘤。此外,根据ICRP110AM和ICRP110AF在223Ra、89Sr、153Sm和32P处理下的活度分别为3.3、148、2220和370 MBq和4.015、148、2701和370 MBq,通过MIRD形式计算吸收剂量。结果:32P作用下的最大骨表面剂量为1.22E+02和8.51E+01 mGy, 223Ra作用下的最小骨表面剂量为8.42E-02和8.26E-02 mGy。在红骨髓、膀胱壁和肾脏剂量比较中,153Sm和89Sr处理的最大剂量分别为2.45E-03、1.500 e -03、3.23E-07、5.45E-06、1.20E-01、1.49E-01 mGy,最小剂量分别为3.46E-05、1.99E-05、6.33E-09、8.77E-09、1.19E-04、1.15E-04 mGy。153Sm组睾丸和卵巢-子宫最大剂量分别为6.17E-08、7.400 e -06、3.46E-07 mGy, 223Ra组睾丸和卵巢最小剂量分别为1.70E-09、1.34E-07 mGy。测定了89Sr治疗时的最小子宫剂量为7.03 ~ 09 mGy。结论:观察到223Ra在治疗疼痛性骨转移中产生低临界器官剂量。在释放β的放射性核素中,89Sr表现出最佳的剂量学结果。
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来源期刊
Current radiopharmaceuticals
Current radiopharmaceuticals PHARMACOLOGY & PHARMACY-
CiteScore
3.20
自引率
4.30%
发文量
43
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