器官和肿瘤剂量测定,包括简化[177Lu]Lu-PSMA-I&T 治疗转移性阉割抵抗性前列腺癌的方法。

IF 3 2区 医学 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
Amir Karimzadeh, Linus Schatz, Markus Sauer, Ivayla Apostolova, Ralph Buchert, Susanne Klutmann, Wencke Lehnert
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引用次数: 0

摘要

背景:个体患者的体内剂量测定对于安全有效的放射性同位素治疗至关重要。精确剂量测定所需的多时间点成像非常耗时,因此对核医学部门和患者的要求都很高。本研究的目的是:(1) 利用全身 SPECT 成像评估[177Lu]Lu-PSMA-I&T 对危险器官和肿瘤病灶的吸收剂量;(2) 研究可能的简化剂量测定方案:这项研究包括 16 名患者,每人接受 4 个周期的[177Lu]Lu-PSMA-I&T 治疗。他们在注射后 2 小时、24 小时、48 小时和 72-168 小时四个时间点(TP)接受了定量全身 SPECT/CT 成像(3 个床位)。对所有患者进行了全三维剂量测定(参考方法),并对有风险的器官(肾脏、腮腺和颌下腺)和每个患者最多十个肿瘤病灶(总共 90 个病灶)进行了剂量循环。简化剂量测定方法(SM)包括:(1) 根据剂量周期 1 的动力学,使用单次 TP 成像生成后续周期的时间活动曲线;对于危险器官,还包括(2) 根据剂量周期 1 和(3) 根据剂量周期 1 和 2 进行简单外推:肾脏、腮腺和颌下腺的归一化吸收剂量分别为 0.71 ± 0.32 mGy/MBq、0.28 ± 0.12 mGy/MBq 和 0.22 ± 0.08 mGy/MBq。肿瘤剂量从剂量周期1的3.86 ± 3.38 mGy/MBq降至剂量周期4的2.01 ± 2.65 mGy/MBq。与全剂量测定方法相比,SM 1 使用单次 TP 成像(48 h p.i.),就每个周期的吸收剂量和总累积剂量而言,对危险器官得出的结果最为准确和精确。对于肿瘤病变,使用第四个 TP(≥ 72 h p.i.)可获得更好的结果:结论:[177Lu]Lu-PSMA-I&T疗法可以简化安全剂量测定方案。如果对肿瘤剂量测定感兴趣,则应使用/添加较晚的成像 TP(≥ 72 h p.i.),以考虑到肿瘤的动力学慢于危险器官。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Organ and tumor dosimetry including method simplification for [177Lu]Lu-PSMA-I&T for treatment of metastatic castration resistant prostate cancer.

Background: Internal dosimetry in individual patients is essential for safe and effective radioligand therapy. Multiple time point imaging for accurate dosimetry is time consuming and hence can be demanding for nuclear medicine departments as well as patients. The objectives of this study were (1) to assess absorbed doses to organs at risk and tumor lesions for [177Lu]Lu-PSMA-I&T using whole body SPECT imaging and (2) to investigate possible simplified dosimetry protocols.

Methods: This study included 16 patients each treated with 4 cycles of [177Lu]Lu-PSMA-I&T. They underwent quantitative whole body SPECT/CT imaging (3 bed positions) at four time points (TP) comprising 2 h, 24 h, 48 h and 72-168 h post-injection (p.i.). Full 3D dosimetry (reference method) was performed for all patients and dose cycles for organs at risk (kidneys, parotid glands and submandibular glands) and up to ten tumor lesions per patient (resulting in 90 lesions overall). The simplified dosimetry methods (SM) included (1) generating time activity curves for subsequent cycles using a single TP of imaging applying the kinetics of dose cycle 1, and for organs at risk also (2) simple extrapolation from dose cycle 1 and (3) from both, dose cycle 1 and 2.

Results: Normalized absorbed doses were 0.71 ± 0.32 mGy/MBq, 0.28 ± 0.12 mGy/MBq and 0.22 ± 0.08 mGy/MBq for kidneys, parotid glands and submandibular glands, respectively. Tumor doses decreased from 3.86 ± 3.38 mGy/MBq in dose cycle 1 to 2.01 ± 2.65 mGy/MBq in dose cycle 4. Compared to the full dosimetry approach the SM 1 using single TP imaging at 48 h p.i. resulted in the most accurate and precise results for the organs at risk in terms of absorbed doses per cycle and total cumulated dose. For tumor lesions better results were achieved using the fourth TP (≥ 72 h p.i.).

Conclusion: Simplification of safety dosimetry protocols is possible for [177Lu]Lu-PSMA-I&T therapy. If tumor dosimetry is of interest a later imaging TP (≥ 72 h p.i.) should be used/added to account for the slower kinetics of tumors compared to organs at risk.

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来源期刊
EJNMMI Physics
EJNMMI Physics Physics and Astronomy-Radiation
CiteScore
6.70
自引率
10.00%
发文量
78
审稿时长
13 weeks
期刊介绍: EJNMMI Physics is an international platform for scientists, users and adopters of nuclear medicine with a particular interest in physics matters. As a companion journal to the European Journal of Nuclear Medicine and Molecular Imaging, this journal has a multi-disciplinary approach and welcomes original materials and studies with a focus on applied physics and mathematics as well as imaging systems engineering and prototyping in nuclear medicine. This includes physics-driven approaches or algorithms supported by physics that foster early clinical adoption of nuclear medicine imaging and therapy.
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