Intercomparison of Treatment Planning Systems (TPS) used in
Radiotherapy: E. Panitsa1, J. C. Rosenwald2, C.
Kappas1 Abstract Advanced techniques in radiotherapy make extensive use of computers for precise planning of the irradiation. It is therefore mandatory to have access 10 TPS which have adequate performances and are fully validated. A cooperative work has been undertaken on this subject within thee framework of thee E.C. BIOMED 1 project DYNARAD. A methodology for the Quality Control of Treatment Planning Systems consisting of three classes of tests (i.e. qualitative tests, internal validation, and quantitative tests of the sophisticated dose calculation features) has been set up. The application of the methodology started with the development of a series of tests for qualitative assessment of dose calculation features such as irregular field, lack of tissue, 2D and 3D inhomogeneity corrections, tray contamination. The protocol was distributed 10 the DYNARAD participants and results from 8 different TPS were obtained. The results showed some limitations of the systems. 1. Introduction TPS which are presently the main computerized tool at the design of the treatment plan in radiotherapy, are getting more and more sophisticated as they integrate advanced features for the realization of modem techniques of conformal radiotherapy. The increasing sophistication results in an increased risk of error. Moreover, the consequences of such errors are of greater importance than in the conventional approach [i]. It is therefore, mandatory to have fully validated TPS with adequate performance in all cases used clinically A working team in the frame of the European project DYNARAD has decided to develop a protocol on Quality Control (QC) of Treatment Planning Systems (TPS), with emphasis to their three dimensional (3D) characteristics. DYNARAD is a three year concerted action project supported by the European Commission, in which 29 Institutions from 10 European countries combine their efforts in the field of "Development and Standardization of New Dynamic Radiotherapy Technics". 2. Method and materials A methodology was developed 12-41 in order to check ail the TPS features in terms of performance and accuracy. The proposed methodology was based on three classes of tests with the following characteristics:
This assessment requires no experimental data. It is a strictly qualitative assessment that examines only if the TPS accounts for a specific feature and not how accurately it performs.
These tests are to determine whether the TPS calculations are consistent with home beam measurements. A list of simple standard situations [5] bas to be decided and tested. Experimental data are required.
Quantitative tests should also be performed for the more sophisticated situations. Experimental data is required that is sometimes difficult to extract. A test protocol containing a series of test cases assessing qualitatively various dose calculation features, was prepared and distributed to the DYNARAD participants, as the first step in the "Quality Control of TPS" [6]. The proposed tests belong to the class I "qualitative assessment" category. These tests are easy to perform by any physicist wishing to check whether its TPS really corporate specific dose calculation features. The tests use the home beam data library. No additional measurements are required. The dose calculation features were selected as the first ones to be included to the protocol, since they are the most crucial characteristics of a TPS. The selected test cases were mostly drawn from the literature [1,7-10], paying special attention to those features which are believed to be weak point of the presently used dose calculation algorithms. The features assessed by the proposed test cases presented in fig. 1, are the following:
The tests were performed by nine institutions participating in the Dynarad project. The following eight TPS's were evaluated: 1. PLATO RTS v I .3 (Acadeinisch Medisch Centrum, Amsterdam, Holland) 2. MODULEX 3000 CMS v2.75 (Borgo Trento Hospital, Verona, Italy) 3. CADPLAN Varian Dosetek v2.62 (University Central Hospital, Helsinki, Finland) 4. HELAX TMS v2.10H (Arhus Kommune hospital, Aarhus, Denmark and Haukeland Hospital, Bergen, Norway) 5. DOSIGRAY v95 (Institut Gustave Roussy, Villejuif, France) 6. CARO (home made) (Instituto Regina Elena, Rome, Italy) 7. MEVAPLAN (University Hospital, Patras, Greece) 8. ISIS-2 V2.0 (Institut Curie, Paris, France) 3. Results The performance of each evaluated TPS is presented in Table I. A brief description of the results [4] for every assessed feature is as follows:
4. Discussion and Conclusion The examined TPS were of a wide variety. Old and modem systems, two dimensional or with three dimensional capabilities, home-made and commercial ones, were included in our tests. As it was expected, a wide range of performances was found. In brief, the following results were taken: · None of the tested systems accounts for electron contamination from tray at the patient surface.· The lateral and longitudinal dimensions of blocks are generally taken into account.· Missing tissues are often accounted for transverse cross sections, but not always for T shape external outlines nor for 3D lack of material. · Only a few systems account for the lateral modification of scatter from inhomogeneity and none for an inhomogeneity described in cross section from the calculation plane. The results showed the expected deficiences of the sytems to give satisfactory results in the more implicated situations of 3D geometries. Their deficiency was in many cases expanded to 2D geometries like lateral inhomogeneities or lack of material. However, even the more modem systems showed limitations in the more complicated cases. system seems to include 3D inhomogeneity correction when the inhomogeneity is described in cross section distant from the calculation plane. As consequence, it was proved that the commercial implementation of sophisticated algorithms can include simplifications that limit the inherent possibilities of these systens. The expansion of the protocol to quantitative tests (i.e. classes 2, and 3 of the proposed methodology) is a future task for the DYNARAD Treatment Planning Group. Another task, being presently under development, is the qualitative test of other features, such as no coplanar beams and dose volume histograms. Acknowledgments We express our thanks to the European Commission supporting our work in DYNARAD concerted action, through the BIOMED I program. Special thanks are also given to the physicists K. Koedooder, G. Chierego, T. Hamalainen, J. J. Christensen and M. S.Thomsen, B. Nygaad, J. Chavaudra and H. Beaudre and G. Nicolazic, M. Benassi and L. Begnozzi, C. Dimou, G. Robineau and M. C. Murillo of the DYNARAD Institutions that performed our test protocol. REFERENCES
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