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Comparing voxel-based absorbed dosimetry methods in tumors, liver, lung, and at the liver-lung interface for (90)Y microsphere selective internal radiation therapy

BACKGROUND: To assess differences between four different voxel-based dosimetry methods (VBDM) for tumor, liver, and lung absorbed doses following (90)Y microsphere selective internal radiation therapy (SIRT) based on (90)Y bremsstrahlung SPECT/CT, a secondary objective was to estimate the sensitivit...

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Detalles Bibliográficos
Autores principales: Mikell, Justin K, Mahvash, Armeen, Siman, Wendy, Mourtada, Firas, Kappadath, S Cheenu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4538912/
https://www.ncbi.nlm.nih.gov/pubmed/26501817
http://dx.doi.org/10.1186/s40658-015-0119-y
Descripción
Sumario:BACKGROUND: To assess differences between four different voxel-based dosimetry methods (VBDM) for tumor, liver, and lung absorbed doses following (90)Y microsphere selective internal radiation therapy (SIRT) based on (90)Y bremsstrahlung SPECT/CT, a secondary objective was to estimate the sensitivity of liver and lung absorbed doses due to differences in organ segmentation near the liver-lung interface. METHODS: Investigated VBDM were Monte Carlo (MC), soft-tissue kernel with density correction (SKD), soft-tissue kernel (SK), and local deposition (LD). Seventeen SIRT cases were analyzed. Mean absorbed doses ([Formula: see text] ) were calculated for tumor, non-tumoral liver (NL), and right lung (RL). Simulations with various SPECT spatial resolutions (FHWMs) and multiple lung shunt fractions (LSs) estimated the accuracy of VBDM at the liver-lung interface. Sensitivity of patient RL and NL [Formula: see text] on segmentation near the interface was assessed by excluding portions near the interface. RESULTS: SKD, SK, and LD were within 5 % of MC for tumor and NL [Formula: see text] . LD and SKD overestimated RL [Formula: see text] compared to MC on average by 17 and 20 %, respectively; SK underestimated RL [Formula: see text] on average by −60 %. Simulations (20 mm FWHM, 20 % LS) showed that SKD, LD, and MC were within 10 % of the truth deep (>39 mm) in the lung; SK significantly underestimated the absorbed dose deep in the lung by approximately −70 %. All VBDM were within 10 % of truth deep (>12 mm) in the liver. Excluding 1, 2, and 3 cm of RL near the interface changed the resulting RL [Formula: see text] by −22, −38, and −48 %, respectively, for all VBDM. An average change of −7 % in the NL [Formula: see text] was realized when excluding 3 cm of NL from the interface. [Formula: see text] was realized when excluding 3 cm of NL from the interface. CONCLUSIONS: SKD, SK, and LD are equivalent to MC for tumor and NL [Formula: see text] . SK underestimates RL [Formula: see text] relative to MC whereas LD and SKD overestimate. RL [Formula: see text] is strongly influenced by the liver-lung interface.