Three-dimensional Monte Carlo-based voxel-wise tumor dosimetry in patients with neuroendocrine tumors who underwent
Autor: | Th I, Goetz, E W, Lang, O, Prante, A, Maier, M, Cordes, T, Kuwert, P, Ritt, Christian, Schmidkonz |
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Rok vydání: | 2019 |
Předmět: |
Male
Radioisotopes Single Photon Emission Computed Tomography Computed Tomography Antineoplastic Agents Radiotherapy Dosage 177Lu-DOTATOC Lutetium Middle Aged Octreotide Monte Carlo simulations Neuroendocrine Tumors Treatment Outcome Dosimetry Organometallic Compounds Chromogranin A Humans Female Original Article Radiopharmaceuticals Radiometry Monte Carlo Method Aged |
Zdroj: | Annals of Nuclear Medicine |
ISSN: | 1864-6433 |
Popis: | Background Patients with advanced neuroendocrine tumors (NETs) of the midgut are suitable candidates for 177Lu-DOTATOC therapy. Integrated SPECT/CT systems have the potential to help improve the accuracy of patient-specific tumor dosimetry. Dose estimations to target organs are generally performed using the Medical Internal Radiation Dose scheme. We present a novel Monte Carlo-based voxel-wise dosimetry approach to determine organ- and tumor-specific total tumor doses (TTD). Methods A cohort of 14 patients with histologically confirmed metastasized NETs of the midgut (11 men, 3 women, 62.3 ± 11.0 years of age) underwent a total of 39 cycles of 177Lu-DOTATOC therapy (mean 2.8 cycles, SD ± 1 cycle). After the first cycle of therapy, regions of interest were defined manually on the SPECT/CT images for the kidneys, the spleen, and all 198 tracer-positive tumor lesions in the field of view. Four SPECT images, taken at 4 h, 24 h, 48 h and 72 h after injection of the radiopharmaceutical, were used to determine their effective half-lives in the structures of interest. The absorbed doses were calculated by a three-dimensional dosimetry method based on Monte Carlo simulations. TTD was calculated as the sum of all products of single tumor doses with single tumor volumes divided by the sum of all tumor volumes. Results The average dose values per cycle were 3.41 ± 1.28 Gy (1.91–6.22 Gy) for the kidneys, 4.40 ± 2.90 Gy (1.14–11.22 Gy) for the spleen, and 9.70 ± 8.96 Gy (1.47–39.49 Gy) for all 177Lu-DOTATOC-positive tumor lesions. Low- and intermediate-grade tumors (G 1–2) absorbed a higher TTD compared to high-grade tumors (G 3) (signed-rank test, p = |
Databáze: | OpenAIRE |
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