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镥-奥曲肽治疗中肾脏解剖体积变化的剂量学意义

Dosimetric implications of kidney anatomical volume changes in Lu-DOTATATE therapy.

作者信息

Khan Jehangir, Rydèn Tobias, Van Essen Martijn, Svensson Johanna, Grudzinski Joseph, Bernhardt Peter

机构信息

Department of Medical Physics and Biomedical Engineering (MFT), Sahlgrenska University Hospital, Gothenburg, SE-41345, Sweden.

Department of Medical Physics, Faculty of Medicine and Health, Örebro University Hospital, Örebro, Sweden.

出版信息

EJNMMI Phys. 2024 Aug 2;11(1):71. doi: 10.1186/s40658-024-00672-w.

Abstract

INTRODUCTION

This study aims to evaluate the use of CT-based whole kidney parenchyma (WKP) segmentation in Lu-DOTATATE dosimetry. Specifically, it investigates whether WKP volumes change during treatment and evaluates the accuracy of applying a single delineated WKP volume for dosimetry. Furthermore, it aims to determine the cause of WKP volume changes-whether caused by radiation or amino acid infusion-by comparing them with spleen volume changes as a marker for radiation-induced alterations.

METHODS

SPECT/CT images of 18 patients were acquired over the abdomen approximately 4 h (h) (D0), 24 h (D1), 48 h (D2) and 168 h (D7) post-administration of Lu-DOTATATE. CT guided WKP volumes were measured before (baseline) and during treatment. Kidney activity concentrations at each time point were derived from CT-segmented WKP overlaid on SPECT scans. The accuracy of using WKP segmentation from a single CT for all time points was assessed against the gold standard of segmenting each WKP individually. Time-integrated activity calculations were based on a tri-exponential curve fit of the kidney activity concentration over time. Kidney absorbed doses were estimated under the assumption of local energy deposition. Additionally, the impact of various partial volume correction methods on dosimetry was evaluated.

RESULTS

Whole-kidney parenchyma (WKP) volumes, ranging from 31 to 243 mL, showed a gradual increase from baseline (mean ± SD = 130.6 ± 46.1 mL) at the initial time points D0 (138.5 ± 44.7 mL) and D1 (139.4 ± 41.6 mL), followed by a slight decrease at D2 (132.8 ± 44.5 mL) and a further decrease at D7 (129.2 ± 42.7 mL). The volume increase at D0 and D1 was statistically significant. Spleen volume did not change during treatment, suggesting that amino acid infusion rather than irradiation effects caused WKP volume changes. Bland-Altman analysis revealed WKP volume biases of 8.77% (D0 vs. B), 10.77% (D1 vs. B), 1.10% (D2 vs. B), and 1.10% (D7 vs. B), with corresponding uncertainties of 24.4%, 23.6%, 25.4%, and 25.4%, respectively. When WKP segmentation from a single CT is applied across all SPECTs, these WKP volume changes could overestimate the activity concentration and mean absorbed doses up to 4.3% and 2.5%, respectively. The absorbed dose uncertainties using a recovery coefficient (RC) of 0.85 for single-time-point WKP delineation increase the absorbed dose uncertainty by 4% compared to the use of patient-specific RCs and time specific segmentation of WKP volumes.

CONCLUSIONS

Kidney volume exhibited significant variation form D0 to D7, affecting the precision of dosimetry calculation, primarily due to errors in whole-kidney parenchyma (WKP) delineation. Notably, using WKP segmentation from a single CT scan applied to sequential SPECT images introduce further uncertainty and may lead to an overestimation of the absorbed dose. The fluctuations in kidney volume are most likely attributable to amino acid infusion.

摘要

引言

本研究旨在评估基于CT的全肾实质(WKP)分割在卢-多他赛(Lu-DOTATATE)剂量测定中的应用。具体而言,它研究了治疗期间WKP体积是否发生变化,并评估了将单个勾勒的WKP体积应用于剂量测定的准确性。此外,它旨在通过将WKP体积变化与作为辐射诱导改变标志物的脾脏体积变化进行比较,确定WKP体积变化的原因——是由辐射还是氨基酸输注引起的。

方法

在注射Lu-DOTATATE后约4小时(D0)、24小时(D1)、48小时(D2)和168小时(D7),对18例患者的腹部进行SPECT/CT成像。在治疗前(基线)和治疗期间测量CT引导下的WKP体积。每个时间点肾脏的活度浓度由叠加在SPECT扫描上的CT分割的WKP得出。将单个CT的WKP分割用于所有时间点的准确性与逐个分割每个WKP的金标准进行比较评估。时间积分活度计算基于肾脏活度浓度随时间的三指数曲线拟合。在局部能量沉积的假设下估计肾脏吸收剂量。此外,评估了各种部分容积校正方法对剂量测定的影响。

结果

全肾实质(WKP)体积范围为31至243 mL,在初始时间点D0(138. ± 44.7 mL)和D1(139.4 ± 41.6 mL)时,相对于基线(平均 ± 标准差 = 130.6 ± 46.1 mL)逐渐增加,随后在D2(132.8 ± 44.5 mL)时略有下降,在D7(129.2 ± 42.7 mL)时进一步下降。D0和D1时的体积增加具有统计学意义。治疗期间脾脏体积未发生变化,这表明是氨基酸输注而非辐射效应导致了WKP体积变化。Bland-Altman分析显示WKP体积偏差在D0与基线(B)相比时为8.77%,D1与基线相比时为10.77%,D2与基线相比时为1.10%,D7与基线相比时为1.10%,相应的不确定度分别为24.4%、23.6%、25.4%和25.4%。当将单个CT的WKP分割应用于所有SPECT时,这些WKP体积变化可能分别使活度浓度和平均吸收剂量高估高达4.3%和2.5%。与使用患者特异性恢复系数(RC)和WKP体积的时间特异性分割相比,在单次时间点WKP勾勒中使用恢复系数(RC)为0.85会使吸收剂量不确定度增加4%。

结论

从D0到D7,肾脏体积表现出显著变化,影响了剂量测定计算的精度,主要是由于全肾实质(WKP)勾勒中的误差。值得注意的是,将单个CT扫描的WKP分割应用于连续的SPECT图像会引入进一步的不确定度,并可能导致吸收剂量的高估。肾脏体积的波动很可能归因于氨基酸输注。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/777a/11294297/530491da2bb0/40658_2024_672_Fig1_HTML.jpg

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