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      Direct aperture optimization: A turnkey solution for step-and-shoot IMRT

      , , , ,
      Medical Physics
      Wiley

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          Abstract

          IMRT treatment plans for step-and-shoot delivery have traditionally been produced through the optimization of intensity distributions (or maps) for each beam angle. The optimization step is followed by the application of a leaf-sequencing algorithm that translates each intensity map into a set of deliverable aperture shapes. In this article, we introduce an automated planning system in which we bypass the traditional intensity optimization, and instead directly optimize the shapes and the weights of the apertures. We call this approach "direct aperture optimization." This technique allows the user to specify the maximum number of apertures per beam direction, and hence provides significant control over the complexity of the treatment delivery. This is possible because the machine dependent delivery constraints imposed by the MLC are enforced within the aperture optimization algorithm rather than in a separate leaf-sequencing step. The leaf settings and the aperture intensities are optimized simultaneously using a simulated annealing algorithm. We have tested direct aperture optimization on a variety of patient cases using the EGS4/BEAM Monte Carlo package for our dose calculation engine. The results demonstrate that direct aperture optimization can produce highly conformal step-and-shoot treatment plans using only three to five apertures per beam direction. As compared with traditional optimization strategies, our studies demonstrate that direct aperture optimization can result in a significant reduction in both the number of beam segments and the number of monitor units. Direct aperture optimization therefore produces highly efficient treatment deliveries that maintain the full dosimetric benefits of IMRT.

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          Most cited references29

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          This paper describes BEAM, a general purpose Monte Carlo code to simulate the radiation beams from radiotherapy units including high-energy electron and photon beams, 60Co beams and orthovoltage units. The code handles a variety of elementary geometric entities which the user puts together as needed (jaws, applicators, stacked cones, mirrors, etc.), thus allowing simulation of a wide variety of accelerators. The code is not restricted to cylindrical symmetry. It incorporates a variety of powerful variance reduction techniques such as range rejection, bremsstrahlung splitting and forcing photon interactions. The code allows direct calculation of charge in the monitor ion chamber. It has the capability of keeping track of each particle's history and using this information to score separate dose components (e.g., to determine the dose from electrons scattering off the applicator). The paper presents a variety of calculated results to demonstrate the code's capabilities. The calculated dose distributions in a water phantom irradiated by electron beams from the NRC 35 MeV research accelerator, a Varian Clinac 2100C, a Philips SL75-20, an AECL Therac 20 and a Scanditronix MM50 are all shown to be in good agreement with measurements at the 2 to 3% level. Eighteen electron spectra from four different commercial accelerators are presented and various aspects of the electron beams from a Clinac 2100C are discussed. Timing requirements and selection of parameters for the Monte Carlo calculations are discussed.
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            Reporting and analyzing dose distributions: A concept of equivalent uniform dose

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              X-ray field compensation with multileaf collimators.

              It has been proposed that conformal therapy can be carried out with static ports that are each individually compensated to deliver an optimal total dose distribution. If this proposal is to be implemented, one must have a means of compensating or modulating the fluence distributions within the boundaries of individual treatment fields. A theory was developed and implemented to achieve this goal. The theory allowed creation of a leaf-setting sequence for a desired level of field-modulation precision. This method of beam modulation was experimentally verified using radiographic film to integrate the dose delivered by the sequence of discrete static multileaf collimator-defined subfields. Beam profiles were generated that matched the planned beam profiles to within the specified degree of precision. This methodology is a candidate for implementation of inverse planning for conformal therapy.
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                Author and article information

                Journal
                Medical Physics
                Med. Phys.
                Wiley
                00942405
                June 2002
                May 13 2002
                May 13 2002
                : 29
                : 6
                : 1007-1018
                Article
                10.1118/1.1477415
                12094970
                f094b377-3009-4370-97b5-04d5a65f0f67
                © 2002

                http://doi.wiley.com/10.1002/tdm_license_1.1

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