Dosimetric characteristics of the DRAXIMAGE model LS-1 1-125 interstitial brachytherapy source design: a Monte Carlo investigation.

Abstract

(Received 5 June 2001; accepted for publication 26 December 2001; published 19 March 2002) We have used Monte Carlo photon transport simulations to evaluate dosimetric characteristics of a new 125I seed, the DRAXIMAGE BrachySeed (model LS-1) source for interstitial brachytherapy and to calculate the dosimetric parameters recommended by the AAPM Task Group 43 (TG-43). To eliminate thick end welds, preformed closed-ended Ti shells are welded together near the transverse plane. The radioactivity is localized near the seed ends in order to maximize isotropy at typical prescription distances. Transmission radiography reveals that its internal components can move by as much as 200 microm under the influence of gravitational forces affecting the dose-rate constant and relative dose distribution by as much as 5% and 10%, respectively. However, the clinical dose distribution can be well represented by a weighted average of dose distributions corresponding to three different orientation-dependent internal geometry configurations. This average dose distribution agrees closely (within 1% at 1 cm) with that derived from the geometry specified by the vendor model (seed components uniformly spaced), from which the recommended relative dosimetry parameters were derived. An average dose-rate constant of 0.935 cGy h(-1) U(-1) is recommended for clinical application and values of 0.919, 0.963, and 0.920 for vertical orientation, horizontal orientation, and the vendor specified geometries, respectively. The NIST wide-angle free-air chamber realization of the air-kerma strength primary standard, SKN99, was explicitly simulated. We show that the output of Ag characteristic x rays is about half that of the model 6711 source resulting in a relative dose distribution between that of the model 6711 source and pure 125I x-ray emitters. Finally, it is demonstrated that the TG-43 point-source formalism more accurately estimates solid-angle weighted dose at small distances if one uses a radial dose function data prepared using a point-source, rather than line-source, geometry factor.