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Radiochromic film dosimetry with flatbed scanners: A fast and accurate method for dose calibration and uniformity correction with single film exposure
Author(s) -
Menegotti L.,
Delana A.,
Martignano A.
Publication year - 2008
Publication title -
medical physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.473
H-Index - 180
eISSN - 2473-4209
pISSN - 0094-2405
DOI - 10.1118/1.2936334
Subject(s) - dosimetry , calibration , scanner , optics , materials science , ionization chamber , dosimeter , nuclear medicine , physics , ionization , medicine , ion , quantum mechanics
Film dosimetry is an attractive tool for dose distribution verification in intensity modulated radiotherapy (IMRT). A critical aspect of radiochromic film dosimetry is the scanner used for the readout of the film: the output needs to be calibrated in dose response and corrected for pixel value and spatial dependent nonuniformity caused by light scattering; these procedures can take a long time. A method for a fast and accurate calibration and uniformity correction for radiochromic film dosimetry is presented: a single film exposure is used to do both calibration and correction. Gafchromic™ EBT films were read with two flatbed charge coupled device scanners (Epson V750 and 1680Pro). The accuracy of the method is investigated with specific dose patterns and an IMRT beam. The comparisons with a two‐dimensional array of ionization chambers using a 18 × 18 cm 2open field and an inverse pyramid dose pattern show an increment in the percentage of points which pass the gamma analysis (tolerance parameters of 3 % and 3 mm), passing from 55 % and 64 % for the 1680Pro and V750 scanners, respectively, to 94 % for both scanners for the 18 × 18 open field, and from 76 % and 75 % to 91 % for the inverse pyramid pattern. Application to an IMRT beam also shows better gamma index results, passing from 88 % and 86 % for the two scanners, respectively, to 94 % for both. The number of points and dose range considered for correction and calibration appears to be appropriate for use in IMRT verification. The method showed to be fast and to correct properly the nonuniformity and has been adopted for routine clinical IMRT dose verification.