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Quantitative assessment of helical tomotherapy plans complexity. | LitMetric

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Article Abstract

Purpose: An unnecessary amount of complexity in radiotherapy plans affects the efficiency of the treatments, increasing the uncertainty of dose deposition and its susceptibility to anatomical changes or setup errors. To date, tools for quantitatively assessing the complexity of tomotherapy plans are still limited. In this study, new metrics were developed to characterize different aspects of helical tomotherapy (HT) plans, and their actual effectiveness was investigated.

Methods: The complexity of 464 HT plans delivered on a Radixact platform was evaluated. A new set of metrics was devised to assess beam geometry, leaf opening time (LOT) variability, and modulation over space and time. Sixty-five complexity metrics were extracted from the dataset using the newly in-house developed software library TCoMX: 29 metrics already proposed in the literature and 36 newly developed metrics. Their reciprocal relation is discussed. Their effectiveness was evaluated through correlation analyses with patient-specific quality assurance (PSQA) results.

Results: An inverse linear relation was found between the average number of closed leaves and the average number of MLC openings and closures as well as between the choice of the modulation factor and the discontinuity of the field, suggesting some intrinsic link between the LOT distribution and the geometrical complexity of the MLC openings. The newly proposed metrics were at least as correlated as the existing ones to the PSQA results. Metrics describing the geometrical complexity of the MLC openings showed the strongest connection to the PSQA results. Significant correlations were found between at least one of the new metrics and the γ index passing rate for six out of seven groups of plans considered.

Conclusion: The new metrics proposed were shown to be effective to characterize more comprehensively the complexity of HT plans. A software library for their automatic extraction is described and made available.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9860001PMC
http://dx.doi.org/10.1002/acm2.13781DOI Listing

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