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(177)Lu-DKFZ-PSMA-617的剂量测定:一种用于治疗转移性前列腺癌的新型放射性药物。

Dosimetry for (177)Lu-DKFZ-PSMA-617: a new radiopharmaceutical for the treatment of metastatic prostate cancer.

作者信息

Delker Andreas, Fendler Wolfgang Peter, Kratochwil Clemens, Brunegraf Anika, Gosewisch Astrid, Gildehaus Franz Josef, Tritschler Stefan, Stief Christian Georg, Kopka Klaus, Haberkorn Uwe, Bartenstein Peter, Böning Guido

机构信息

Department of Nuclear Medicine, Ludwig-Maximilians-University of Munich, Marchioninistrasse 15, 81377, Munich, Germany.

Department for Nuclear Medicine, Heidelberg University Hospital, Heidelberg, Germany.

出版信息

Eur J Nucl Med Mol Imaging. 2016 Jan;43(1):42-51. doi: 10.1007/s00259-015-3174-7. Epub 2015 Aug 29.

Abstract

PURPOSE

Dosimetry is critical to achieve the optimal therapeutic effect of radioligand therapy (RLT) with limited side effects. Our aim was to perform image-based absorbed dose calculation for the new PSMA ligand (177)Lu-DKFZ-PSMA-617 in support of its use for the treatment of metastatic prostate cancer.

METHODS

Whole-body planar images and SPECT/CT images of the abdomen were acquired in five patients (mean age 68 years) for during two treatment cycles at approximately 1, 24, 48 and 72 h after administration of 3.6 GBq (range 3.4 to 3.9 GBq) (177)Lu-DKFZ-PSMA-617. Quantitative 3D SPECT OSEM reconstruction was performed with corrections for photon scatter, photon attenuation and detector blurring. A camera-specific calibration factor derived from phantom measurements was used for quantitation. Absorbed doses were calculated for various organs from the images using a combination of linear approximation, exponential fit, and target-specific S values, in accordance with the MIRD scheme. Absorbed doses to bone marrow were estimated from planar and SPECT images and with consideration of the blood sampling method according to the EANM guidelines.

RESULTS

The average (± SD) absorbed doses per cycle were 2.2 ± 0.6 Gy for the kidneys (0.6 Gy/GBq), 5.1 ± 1.8 Gy for the salivary glands (1.4 Gy/GBq), 0.4 ± 0.2 Gy for the liver (0.1 Gy/GBq), 0.4 ± 0.1 Gy for the spleen (0.1 Gy/GBq), and 44 ± 19 mGy for the bone marrow (0.012 Gy/GBq). The organ absorbed doses did not differ significantly between cycles. The critical absorbed dose reported for the kidneys (23 Gy) was not reached in any patient. At 24 h there was increased uptake in the colon with 50 - 70 % overlap to the kidneys on planar images. Absorbed doses for tumour lesions ranged between 1.2 and 47.5 Gy (13.1 Gy/GBq) per cycle.

CONCLUSION

The salivary glands and kidneys showed high, but not critical, absorbed doses after RLT with (177)Lu-DKFZ-PSMA-617. We suggest that (177)Lu-DKFZ-PSMA-617 is suitable for radiotherapy, offering tumour-to-kidney ratios comparable to those with RLT agents currently available for the treatment of neuroendocrine tumours. Our dosimetry results suggest that (177)Lu-DKFZ-PSMA-617 treatment with higher activities and more cycles is possible without the risk of damaging the kidneys.

摘要

目的

剂量测定对于在副作用有限的情况下实现放射性配体疗法(RLT)的最佳治疗效果至关重要。我们的目的是对新型PSMA配体(177)Lu-DKFZ-PSMA-617进行基于图像的吸收剂量计算,以支持其用于治疗转移性前列腺癌。

方法

在5名患者(平均年龄68岁)中,于给予3.6GBq(范围3.4至3.9GBq)(177)Lu-DKFZ-PSMA-617后的大约1、24、48和72小时,在两个治疗周期内采集全身平面图像和腹部SPECT/CT图像。进行定量三维SPECT OSEM重建,并校正光子散射、光子衰减和探测器模糊。使用从体模测量得出的特定相机校准因子进行定量。根据MIRD方案,结合线性近似、指数拟合和特定靶区的S值,从图像中计算各个器官的吸收剂量。根据EANM指南,从平面图像和SPECT图像估计骨髓吸收剂量,并考虑血液采样方法。

结果

每个周期的平均(±标准差)吸收剂量为:肾脏2.2±0.6Gy(0.6Gy/GBq),唾液腺5.1±1.8Gy(1.4Gy/GBq),肝脏0.4±0.2Gy(0.1Gy/GBq),脾脏0.4±0.1Gy(0.1Gy/GBq),骨髓44±19mGy(0.012Gy/GBq)。各周期之间器官吸收剂量无显著差异。任何患者均未达到报道的肾脏临界吸收剂量(23Gy)。在24小时时,结肠摄取增加,平面图像上与肾脏的重叠率为50%-70%。肿瘤病灶的吸收剂量每个周期在1.2至47.5Gy(13.1Gy/GBq)之间。

结论

(177)Lu-DKFZ-PSMA-617进行RLT后,唾液腺和肾脏显示出较高但非临界的吸收剂量。我们认为(177)Lu-DKFZ-PSMA-617适用于放射治疗,其肿瘤与肾脏的比值与目前可用于治疗神经内分泌肿瘤的RLT药物相当。我们的剂量测定结果表明,使用更高活度和更多周期的(177)Lu-DKFZ-PSMA-617进行治疗是可行的,且不会有损害肾脏的风险。

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