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肽受体放射性核素治疗中预测剂量与实际吸收剂量的差异。

Differences in predicted and actually absorbed doses in peptide receptor radionuclide therapy.

机构信息

Klinik für Nuklearmedizin, Universität Ulm, Ulm, Germany.

出版信息

Med Phys. 2012 Sep;39(9):5708-17. doi: 10.1118/1.4747266.

Abstract

PURPOSE

An important assumption in dosimetry prior to radionuclide therapy is the equivalence of pretherapeutic and therapeutic biodistribution. In this study the authors investigate if this assumption is justified in sst2-receptor targeting peptide therapy, as unequal amounts of peptide and different peptides for pretherapeutic measurements and therapy are commonly used.

METHODS

Physiologically based pharmacokinetic models were developed. Gamma camera and serum measurements of ten patients with metastasizing neuroendocrine tumors were conducted using (111)In-DTPAOC. The most suitable model was selected using the corrected Akaike information criterion. Based on that model and the estimated individual parameters, predicted and measured (90)Y-DOTATATE excretions during therapy were compared. The residence times for the pretherapeutic (measured) and therapeutic scenarios (simulated) were calculated.

RESULTS

Predicted and measured therapeutic excretion differed in three patients by 10%, 31%, and 7%. The measured pretherapeutic and therapeutic excretion differed by 53%, 56%, and 52%. The simulated therapeutic residence times of kidney and tumor were 3.1 ± 0.6 and 2.5 ± 1.2 fold higher than the measured pretherapeutic ones.

CONCLUSIONS

To avoid the introduction of unnecessary inaccuracy in dosimetry, using the same substance along with the same amount for pretherapeutic measurements and therapy is recommended.

摘要

目的

放射性核素治疗前的剂量学有一个重要的假设,即治疗前和治疗时的生物分布等效。在这项研究中,作者研究了在 sst2 受体靶向肽治疗中,这一假设是否成立,因为通常会使用不同数量的肽和不同的肽进行治疗前测量和治疗。

方法

开发了基于生理学的药代动力学模型。使用 (111)In-DTPAOC 对 10 名转移性神经内分泌肿瘤患者进行了伽马相机和血清测量。使用校正的 Akaike 信息准则选择最合适的模型。基于该模型和估计的个体参数,比较了治疗期间预测的和测量的 (90)Y-DOTATATE 排泄。计算了治疗前(测量)和治疗(模拟)情况下的停留时间。

结果

在 3 名患者中,预测的和测量的治疗排泄量差异分别为 10%、31%和 7%。测量的治疗前和治疗排泄量差异分别为 53%、56%和 52%。模拟的肾脏和肿瘤的治疗停留时间分别比测量的治疗前停留时间高 3.1 ± 0.6 倍和 2.5 ± 1.2 倍。

结论

为了避免在剂量学中引入不必要的不准确性,建议在治疗前测量和治疗中使用相同的物质和相同的量。

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