In vivo dosimetry (IVD) is the last step of a radiotherapy quality control program aimed to ensure that the dose delivered is in agreement with that prescribed. IVD procedures based on single detectors are time-consuming and impossible to use for the modern radiotherapy techniques, based on static or kinetic beams (modulated in intensity fluence); this means that more efficient and practical methods are highly recommended. The practical method SOFTDISO, based on the use of electronic portal image device (EPID), provides two tests (i) the R ratio between the reconstructed and the planned isocenter doses to verify an agreement within 5% and (ii) the γ-analysis of the EPID images, to verify γ% ≥ 90% and γmean ≤ 0.4. This paper reports the results of 11,357 IVD tests carried out for 823 patients treated by three-dimensional conformal radiation therapy and volumetric modulated arc therapy techniques. In particular, the dose disagreements are reported distinguishing two kinds of causes, those of (i) class 1 that includes the errors due to inadequate quality controls and (ii) the class 2, due to patient morphological changes. About the tests out of tolerance, 6% were by VMAT and 21% by 3DCRT, but taking into account the only class 1 of errors, i.e., removing the causes of class 2, only 7% of patients examined presented at least one of the three mean indexes out of tolerance. The workload for IVD on 9 patients/day per linac is about 52 min/day but recently, a new automated SOFTDISO version has been implemented to reduce the time to about 34 min/day.

Piermattei, A., Greco, F., Grusio, M., Menna, S., Azario, L., Stimato, G., Placidi, E., Teodoli, S., Cilla, S., Porcelli, A., Alberico, L., Fidanzio, A., A validation study of a dedicated software for an automated in vivo dosimetry control in radiotherapy, <<MEDICAL & BIOLOGICAL ENGINEERING & COMPUTING>>, 2018; 56 (10): 1939-1947. [doi:10.1007/s11517-018-1822-3] [http://hdl.handle.net/10807/172187]

A validation study of a dedicated software for an automated in vivo dosimetry control in radiotherapy

Piermattei, A.;Azario, L.;Stimato, G.;Placidi, E.;Cilla, S.;Alberico, L.;Fidanzio, A.
2018

Abstract

In vivo dosimetry (IVD) is the last step of a radiotherapy quality control program aimed to ensure that the dose delivered is in agreement with that prescribed. IVD procedures based on single detectors are time-consuming and impossible to use for the modern radiotherapy techniques, based on static or kinetic beams (modulated in intensity fluence); this means that more efficient and practical methods are highly recommended. The practical method SOFTDISO, based on the use of electronic portal image device (EPID), provides two tests (i) the R ratio between the reconstructed and the planned isocenter doses to verify an agreement within 5% and (ii) the γ-analysis of the EPID images, to verify γ% ≥ 90% and γmean ≤ 0.4. This paper reports the results of 11,357 IVD tests carried out for 823 patients treated by three-dimensional conformal radiation therapy and volumetric modulated arc therapy techniques. In particular, the dose disagreements are reported distinguishing two kinds of causes, those of (i) class 1 that includes the errors due to inadequate quality controls and (ii) the class 2, due to patient morphological changes. About the tests out of tolerance, 6% were by VMAT and 21% by 3DCRT, but taking into account the only class 1 of errors, i.e., removing the causes of class 2, only 7% of patients examined presented at least one of the three mean indexes out of tolerance. The workload for IVD on 9 patients/day per linac is about 52 min/day but recently, a new automated SOFTDISO version has been implemented to reduce the time to about 34 min/day.
2018
Inglese
Piermattei, A., Greco, F., Grusio, M., Menna, S., Azario, L., Stimato, G., Placidi, E., Teodoli, S., Cilla, S., Porcelli, A., Alberico, L., Fidanzio, A., A validation study of a dedicated software for an automated in vivo dosimetry control in radiotherapy, <<MEDICAL & BIOLOGICAL ENGINEERING & COMPUTING>>, 2018; 56 (10): 1939-1947. [doi:10.1007/s11517-018-1822-3] [http://hdl.handle.net/10807/172187]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10807/172187
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