Monte Carlo simulation;
Targeted radionuclide therapy;
Terbium-161;
Lutetium-177;
Micrometastases;
TARGETED RADIONUCLIDE THERAPY;
BETA-EMITTING RADIONUCLIDES;
MULTICELLULAR DOSIMETRY;
S VALUES;
RADIOIMMUNOTHERAPY;
ENERGY;
D O I:
10.1186/s40658-020-00301-2
中图分类号:
R8 [特种医学];
R445 [影像诊断学];
学科分类号:
1002 ;
100207 ;
1009 ;
摘要:
Background Targeted radionuclide therapy (TRT) is gaining importance. For TRT to be also used as adjuvant therapy or for treating minimal residual disease, there is a need to increase the radiation dose to small tumours. The aim of this in silico study was to compare the performances of Tb-161 (a medium-energy beta(-) emitter with additional Auger and conversion electron emissions) and Lu-177 for irradiating single tumour cells and micrometastases, with various distributions of the radionuclide. Methods We used the Monte Carlo track-structure (MCTS) code CELLDOSE to compute the radiation doses delivered by Tb-161 and Lu-177 to single cells (14 mu m cell diameter with 10 mu m nucleus diameter) and to a tumour cluster consisting of a central cell surrounded by two layers of cells (18 neighbours). We focused the analysis on the absorbed dose to the nucleus of the single tumoral cell and to the nuclei of the cells in the cluster. For both radionuclides, the simulations were run assuming that 1 MeV was released per mu m(3) (1436 MeV/cell). We considered various distributions of the radionuclides: either at the cell surface, intracytoplasmic or intranuclear. Results For the single cell, the dose to the nucleus was substantially higher with Tb-161 compared to Lu-177, regardless of the radionuclide distribution: 5.0 Gy vs. 1.9 Gy in the case of cell surface distribution; 8.3 Gy vs. 3.0 Gy for intracytoplasmic distribution; and 38.6 Gy vs. 10.7 Gy for intranuclear location. With the addition of the neighbouring cells, the radiation doses increased, but remained consistently higher for Tb-161 compared to Lu-177. For example, the dose to the nucleus of the central cell of the cluster was 15.1 Gy for Tb-161 and 7.2 Gy for Lu-177 in the case of cell surface distribution of the radionuclide, 17.9 Gy for Tb-161 and 8.3 Gy for Lu-177 for intracytoplasmic distribution and 47.8 Gy for Tb-161 and 15.7 Gy for Lu-177 in the case of intranuclear location. Conclusion Tb-161 should be a better candidate than Lu-177 for irradiating single tumour cells and micrometastases, regardless of the radionuclide distribution.
机构:
Univ Gothenburg, Dept Med Radiat Sci, Gothenburg, SwedenUniv Gothenburg, Dept Med Radiat Sci, Gothenburg, Sweden
Hemmingsson, J.
Nestor, M.
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机构:
Uppsala Univ, Dept Immunol Genet & Pathol, Sci Life Lab SciLifeLab, Uppsala, SwedenUniv Gothenburg, Dept Med Radiat Sci, Gothenburg, Sweden
Nestor, M.
Mortensen, A. Lundgren
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Uppsala Univ, Dept Immunol Genet & Pathol, Sci Life Lab SciLifeLab, Uppsala, Sweden
Karolinska Inst, Dept Mol Med & Surg, Stockholm, SwedenUniv Gothenburg, Dept Med Radiat Sci, Gothenburg, Sweden
Mortensen, A. Lundgren
Svensson, J.
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机构:
Sahlgrens Univ Hosp, Dept Oncol, Gothenburg, SwedenUniv Gothenburg, Dept Med Radiat Sci, Gothenburg, Sweden
机构:
Univ Ulsan, Coll Med, Asan Med Ctr, Dept Nucl Med, Seoul, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Nucl Med, Seoul, South Korea
Ha, Sejin
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Kim, Yong-il
Oh, Jungsu S.
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Univ Ulsan, Coll Med, Asan Med Ctr, Dept Nucl Med, Seoul, South Korea
Asan Med Ctr, Asan Canc Inst, Theranost Ctr, Seoul, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Nucl Med, Seoul, South Korea
Oh, Jungsu S.
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Yoo, Changhoon
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Ryoo, Baek-Yeol
Ryu, Jin-Sook
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机构:
Univ Ulsan, Coll Med, Asan Med Ctr, Dept Nucl Med, Seoul, South Korea
Asan Med Ctr, Asan Canc Inst, Theranost Ctr, Seoul, South KoreaUniv Ulsan, Coll Med, Asan Med Ctr, Dept Nucl Med, Seoul, South Korea