Abstract

The purpose of this work was to develop an end-to-end patient-specific quality assurance (QA) technique for spot-scanned proton therapy that is more sensitive and efficient than traditional approaches. The patient-specific methodology relies on independently verifying the accuracy of the delivered proton fluence and the dose calculation in the heterogeneous patient volume. A Monte Carlo dose calculation engine, which was developed in-house, recalculates a planned dose distribution on the patient CT data set to verify the dose distribution represented by the treatment planning system. The plan is then delivered in a pre-treatment setting and logs of spot position and dose monitors, which are integrated into the treatment nozzle, are recorded. A computational routine compares the delivery log to the DICOM spot map used by the Monte Carlo calculation to ensure that the delivered parameters at the machine match the calculated plan. Measurements of dose planes using independent detector arrays, which historically are the standard approach to patient-specific QA, are not performed for every patient. The nozzle-integrated detectors are rigorously validated using independent detectors in regular QA intervals. The measured data are compared to the expected delivery patterns. The dose monitor reading deviations are reported in a histogram, while the spot position discrepancies are plotted vs. spot number to facilitate independent analysis of both random and systematic deviations. Action thresholds are linked to accuracy of the commissioned delivery system. Even when plan delivery is acceptable, the Monte Carlo second check system has identified dose calculation issues which would not have been illuminated using traditional, phantom-based measurement techniques. The efficiency and sensitivity of our patient-specific QA program has been improved by implementing a procedure which independently verifies patient dose calculation accuracy and plan delivery fidelity. Such an approach to QA requires holistic integration and maintenance of patient-specific and patient-independent QA.

Highlights

  • Deviations between intended and delivered radiotherapy dose distributions can potentially lead to severe clinical consequences [1]

  • The main elements of PSQA include verifying that 1) the treatment planning system (TPS) correctly models the radiation fluence produced by the treatment machine, 2) the machine performance is acceptable to deliver the intended fluence, 3) the TPS calculates an accurate representation of the dose delivered to the patient, and 4) the plan data, which is transferred between the TPS and the treatment delivery system via DICOM, is complete and interpreted correctly [4,5]

  • AAPM Task Group 218 has recommended that true composite dose distributions be measured in water-like phantoms for routine intensity modulated radiation therapy (IMRT) quality assurance (QA), with an action threshold corresponding to 90% of measured points passing a gamma criteria of 3% / 2mm [11]

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Summary

Introduction

Deviations between intended and delivered radiotherapy dose distributions can potentially lead to severe clinical consequences [1]. The main elements of PSQA include verifying that 1) the treatment planning system (TPS) correctly models the radiation fluence produced by the treatment machine, 2) the machine performance is acceptable to deliver the intended fluence, 3) the TPS calculates an accurate representation of the dose delivered to the patient, and 4) the plan data, which is transferred between the TPS and the treatment delivery system via DICOM, is complete and interpreted correctly [4,5] All of these potential issues are implicitly verified in traditional, end-to-end phantom measurements, which are the traditional convention for PSQA. Regions of failures should be further investigated to assess the clinical relevance of the measured deviations

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