Estimate of absorbed dose based on two-dimensional autoradiographic information in internal radionuclide therapy

Citation
Xq. Lu et al., Estimate of absorbed dose based on two-dimensional autoradiographic information in internal radionuclide therapy, MED PHYS, 28(3), 2001, pp. 328-335
Citations number
22
Categorie Soggetti
Radiology ,Nuclear Medicine & Imaging","Medical Research Diagnosis & Treatment
Journal title
MEDICAL PHYSICS
ISSN journal
00942405 → ACNP
Volume
28
Issue
3
Year of publication
2001
Pages
328 - 335
Database
ISI
SICI code
0094-2405(200103)28:3<328:EOADBO>2.0.ZU;2-M
Abstract
In radiation therapies using radionuclides emitting short-range particles, such as radioimmunotherapy or boron neutron capture therapy, the biological effects are strongly affected by the heterogeneity of the absorbed dose di stribution delivered to tumor cells. The three-dimensional (3D) information of the source distribution at the cellular level is required to accurately determine the absorbed dose distribution to the individual tumor cells. Tw o-dimensional distribution of cell and nuclide with a resolution of 1 mum c an be obtained from individual tissue sections by microautoradiography. To obtain such information in 3D, an ideal approach would be to align the seri al tissue sections from a block and analyze all of them. This is straightfo rward in theory, but extremely difficult in practice. Furthermore, every se ction in the block has to be processed and analyzed, and the usage of the d ata from this laborious work is very inefficient. An approach presented her e is to estimate the absorbed dose based on individual sections without 3D reconstruction. It is realistically workable since it avoids the most diffi cult task of alignment for the serial tissue sections. In addition, the abs orbed dose can be estimated based on a limited number of noncontiguous sect ions. The validity of this approach has been tested by a Monte Carlo simula tion for two representative radionuclide configurations: (a) a uniform dist ribution of sources and (b) a cell membrane bound source distribution. With only a limited number of sampling sections, the uncertainties in the dose estimation were estimated to similar to 15% for short-range particles. (C) 2001 American Association of Physicists in Medicine. [DOI: 10.1118/1.135058 4].