Dept. Nuclear Medicine, Inselspital, Bern University Hospital, University of Bern, Bern, Switzerland.
Dept. Nuclear Medicine, Technical University of Munich, Munich, Germany.
Eur J Nucl Med Mol Imaging. 2022 Oct;49(12):4064-4072. doi: 10.1007/s00259-022-05883-w. Epub 2022 Jun 30.
Although treatment planning and individualized dose application for emerging prostate-specific membrane antigen (PSMA)-targeted radioligand therapy (RLT) are generally recommended, it is still difficult to implement in practice at the moment. In this study, we aimed to prove the concept of pretherapeutic prediction of dosimetry based on imaging and laboratory measurements before the RLT treatment.
Twenty-three patients with metastatic castration-resistant prostate cancer (mCRPC) treated with Lu-PSMA I&T RLT were included retrospectively. They had available pre-therapy Ga-PSMA-HEBD-CC PET/CT and at least 3 planar and 1 SPECT/CT imaging for dosimetry. Overall, 43 cycles of Lu-PSMA I&T RLT were applied. Organ-based standard uptake values (SUVs) were obtained from pre-therapy PET/CT scans. Patient dosimetry was calculated for the kidney, liver, spleen, and salivary glands using Hermes Hybrid Dosimetry 4.0 from the planar and SPECT/CT images. Machine learning methods were explored for dose prediction from organ SUVs and laboratory measurements. The uncertainty of these dose predictions was compared with the population-based dosimetry estimates. Mean absolute percentage error (MAPE) was used to assess the prediction uncertainty of estimated dosimetry.
An optimal machine learning method achieved a dosimetry prediction MAPE of 15.8 ± 13.2% for the kidney, 29.6% ± 13.7% for the liver, 23.8% ± 13.1% for the salivary glands, and 32.1 ± 31.4% for the spleen. In contrast, the prediction based on literature population mean has significantly larger MAPE (p < 0.01), 25.5 ± 17.3% for the kidney, 139.1% ± 111.5% for the liver, 67.0 ± 58.3% for the salivary glands, and 54.1 ± 215.3% for the spleen.
The preliminary results confirmed the feasibility of pretherapeutic estimation of treatment dosimetry and its added value to empirical population-based estimation. The exploration of dose prediction may support the implementation of treatment planning for RLT.
虽然新兴的前列腺特异性膜抗原(PSMA)靶向放射性配体治疗(RLT)的治疗计划和个体化剂量应用通常是推荐的,但目前在实践中仍难以实施。在这项研究中,我们旨在证明在 RLT 治疗前基于影像学和实验室测量进行治疗前剂量预测的概念。
回顾性纳入 23 例接受 Lu-PSMA I&T RLT 治疗的转移性去势抵抗性前列腺癌(mCRPC)患者。他们在治疗前有 Ga-PSMA-HEBD-CC PET/CT 检查,并且至少有 3 次平面和 1 次 SPECT/CT 成像用于剂量测定。总共应用了 43 个 Lu-PSMA I&T RLT 周期。从治疗前的 PET/CT 扫描中获得器官的标准化摄取值(SUV)。使用 Hermes Hybrid Dosimetry 4.0 从平面和 SPECT/CT 图像中计算患者的肾脏、肝脏、脾脏和唾液腺剂量。探索了从器官 SUV 和实验室测量值预测剂量的机器学习方法。将这些剂量预测的不确定性与基于人群的剂量估计进行了比较。平均绝对百分比误差(MAPE)用于评估估计剂量的预测不确定性。
最佳的机器学习方法对肾脏的剂量预测具有 15.8±13.2%的 MAPE,对肝脏的剂量预测具有 29.6%±13.7%的 MAPE,对唾液腺的剂量预测具有 23.8%±13.1%的 MAPE,对脾脏的剂量预测具有 32.1%±31.4%的 MAPE。相比之下,基于文献人群均值的预测具有显著更大的 MAPE(p<0.01),对肾脏的 MAPE 为 25.5±17.3%,对肝脏的 MAPE 为 139.1%±111.5%,对唾液腺的 MAPE 为 67.0%±58.3%,对脾脏的 MAPE 为 54.1%±215.3%。
初步结果证实了治疗前剂量估计的可行性及其对经验性基于人群的估计的附加值。对剂量预测的探索可能支持 RLT 的治疗计划的实施。