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首页> 外文期刊>The Journal of Nuclear Medicine >Tumor-Absorbed Dose for Non-Hodgkin Lymphoma Patients Treated with the Anti-CD37 Antibody Radionuclide Conjugate 177Lu-Lilotomab Satetraxetan
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Tumor-Absorbed Dose for Non-Hodgkin Lymphoma Patients Treated with the Anti-CD37 Antibody Radionuclide Conjugate 177Lu-Lilotomab Satetraxetan

机译:抗CD37抗体放射性核素结合177Lu-Lilotomab沙丁西坦治疗的非霍奇金淋巴瘤患者的肿瘤吸收剂量

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id="p-2">177Lu-lilotomab satetraxetan is a novel antibody radionuclide conjugate currently tested in a phase 1/2a first-in-human dosage escalation trial for patients with relapsed CD37+ indolent non-Hodgkin lymphoma. The aim of this work was to develop dosimetric methods and calculate tumor-absorbed radiation doses for patients treated with 177Lu-lilotomab satetraxetan. >Methods: Patients were treated at escalating injected activities (10, 15 and 20 MBq/kg) of 177Lu-lilotomab satetraxetan and with different predosing, with or without 40 mg of unlabeled lilotomab. Eight patients were included for the tumor dosimetry study. Tumor radioactivity concentrations were calculated from SPECT acquisitions at multiple time points, and tumor masses were delineated from corresponding CT scans. Tumor-absorbed doses were then calculated using the OLINDA sphere model. To perform voxel dosimetry, the SPECT/CT data and an in-house-developed MATLAB program were combined to investigate the dose rate homogeneity. >Results: Twenty-six tumors in 8 patients were ascribed a mean tumor-absorbed dose. Absorbed doses ranged from 75 to 794 cGy, with a median of 264 cGy across different dosage levels and different predosing. A significant correlation between the dosage level and tumor-absorbed dose was found. Twenty-one tumors were included for voxel dosimetry and parameters describing dose-volume coverage calculated. The investigation of intratumor voxel doses indicates that mean tumor dose is correlated to these parameters. >Conclusion: Tumor-absorbed doses for patients treated with 177Lu-lilotomab satetraxetan are comparable to doses reported for other radioimmunotherapy compounds. Although the intertumor variability was considerable, a correlation between tumor dose and patient dosage level was found. Our results indicate that mean dose may be used as the sole dosimetric parameter on the lesion level.
机译:id =“ p-2”> 177 Lu-lilotomab satetraxetan是一种新型抗体放射性核素偶联物,目前已在1 / 2a期首次人用剂量递增试验中针对复发性CD37 +惰性患者进行了测试非霍奇金淋巴瘤。这项工作的目的是为 177 Lu-lilotomab沙曲西坦治疗的患者开发剂量测定方法并计算肿瘤吸收的辐射剂量。 >方法:患者接受递增剂量的 177 Lu-lilotomab satetraxetan的注射活动(10、15和20 MBq / kg)治疗,并且有不同的剂量,有或没有40 mg未标记的lilotomab。包括八名患者进行肿瘤剂量测定研究。通过在多个时间点的SPECT采集来计算肿瘤放射性浓度,并从相应的CT扫描中描绘出肿瘤块。然后使用OLINDA球形模型计算肿瘤吸收剂量。为了进行体素剂量测定,将SPECT / CT数据和内部开发的MATLAB程序结合起来研究剂量率均匀性。 >结果:将8例患者中的26例肿瘤归因于平均肿瘤吸收剂量。吸收剂量的范围为75至794 cGy,不同剂量水平和不同剂量的中位剂量为264 cGy。发现剂量水平和肿瘤吸收剂量之间显着相关。包括21个肿瘤用于体素剂量测定,并计算了描述剂量-体积覆盖率的参数。肿瘤内体素剂量的研究表明平均肿瘤剂量与这些参数相关。 >结论:用 177 Lu-lilotomab satetraxetan治疗的患者的肿瘤吸收剂量与报道的其他放射免疫疗法化合物的剂量相当。尽管肿瘤间的差异很大,但发现肿瘤剂量与患者剂量水平之间存在相关性。我们的结果表明,平均剂量可用作病变水平的唯一剂量参数。

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