Literature DB >> 27482153

Validation and clinical implementation of commercial secondary check software with heterogeneity corrections.

Vijayalakshmi Kuppusamy1, Vivekanandan Nagarajan1, Lavanya Murugan1.   

Abstract

AIM: To validate and implement PTW diamond secondary check software (SCS) in a routine clinical use.
BACKGROUND: The secondary independent monitor unit or dose calculation verifications have led to a significant increase in the workflow associated with QA treatments. Modelling, validation and commissioning are necessary steps thereby making it a useful tool for QA.
MATERIALS AND METHODS: PTW Diamond SCS is capable of calculating VMAT fields, based on modified Clarkson integration, accounting for multi-leaf collimators (MLC) transmission and measured collimator scatter factors. Validation for heterogeneity corrections is made using circular phantom with inserts of various density materials. 150 VMAT plans were compared using (i) plans calculated in homogeneous cylindrical phantom and (ii) VMAT plans calculated with heterogeneity corrections using electron density values for each organ.
RESULTS: Diamond SCS calculated dose for homogeneous cylindrical phantom resulted in average deviation of (0.1 ± 2.14%) with Eclipse TPS calculated dose and (-2.0 ± 1.66%) with absolute measured dose. PTW's OCTAVIUS-4D phantom with 729 ion chamber detector array measurements agreed well with Eclipse TPS calculated dose showing an average deviation of (-1.69 ± 1.56%). Diamond SCS dose calculations were performed with heterogeneity corrections for 124 VMAT plans with isocentre at a region above -350 HU. The overall MU variations between Diamond SCS and TPS Acuros-XB algorithms were within ±5%.
CONCLUSION: Hence, the Diamond SCS can be used as an additional tool along with phantom measurements for patient specific quality assurance of VMAT plans with heterogeneity corrections having isocentre at a region above -350 HU.

Entities:  

Keywords:  Diamond SCS; Heterogeneity corrections; VMAT

Year:  2016        PMID: 27482153      PMCID: PMC4956914          DOI: 10.1016/j.rpor.2016.06.003

Source DB:  PubMed          Journal:  Rep Pract Oncol Radiother        ISSN: 1507-1367


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