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Portability of IMRT QA between matched linear accelerators.

Publication ,  Journal Article
Barraclough, B; Labby, ZE; Frigo, SP
Published in: J Appl Clin Med Phys
September 9, 2024

PURPOSE: To determine if patient-specific IMRT quality assurance can be measured on any matched treatment delivery system (TDS) for patient treatment delivery on another. METHODS: Three VMAT plans of varying complexity were created for each available energy for head and neck, SBRT lung, and right chestwall anatomical sites. Each plan was delivered on three matched Varian TrueBeam TDSs to the same Scandidos Delta4 Phantom+ diode array with only energy-specific device calibrations. Dose distributions were corrected for TDS output and then compared to TPS calculations using gamma analysis. Round-robin comparisons between measurements from each TDS were also performed using point-by-point dose difference, median dose difference, and the percent of point dose differences within 2% of the mean metrics. RESULTS: All plans had more than 95% of points passing a gamma analysis using 3%/3 mm criteria with global normalization and a 20% threshold when comparing measurements to calculations. The tightest gamma analysis criteria where a plan still passed > 95% were similar across delivery systems-within 0.5%/0.5 mm for all but three plan/energy combinations. Median dose deviations in measurement-to-measurement comparisons were within 0.7% and 1.0% for global and local normalization, respectively. More than 90% of the point differences were within 2%. CONCLUSION: A set of plans spanning available energies and complexity levels were delivered by three matched TDSs. Comparisons to calculations and between measurements showed dose distributions delivered by each TDS using the same DICOM RT-plan file meet tolerances much smaller than typical clinical IMRT QA criteria. This demonstrates each TDS is modeled to a similar accuracy by a common class (shared) beam model. Additionally, it demonstrates that dose distributions from one TDS show small differences in median dose to the others. This is an important validation component of the common beam model approach, allowing for operational improvements in the clinic.

Duke Scholars

Published In

J Appl Clin Med Phys

DOI

EISSN

1526-9914

Publication Date

September 9, 2024

Start / End Page

e14492

Location

United States

Related Subject Headings

  • Nuclear Medicine & Medical Imaging
  • 5105 Medical and biological physics
  • 3208 Medical physiology
  • 1116 Medical Physiology
  • 1103 Clinical Sciences
  • 0299 Other Physical Sciences
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Barraclough, B., Labby, Z. E., & Frigo, S. P. (2024). Portability of IMRT QA between matched linear accelerators. J Appl Clin Med Phys, e14492. https://doi.org/10.1002/acm2.14492
Barraclough, Brendan, Zacariah E. Labby, and Sean P. Frigo. “Portability of IMRT QA between matched linear accelerators.J Appl Clin Med Phys, September 9, 2024, e14492. https://doi.org/10.1002/acm2.14492.
Barraclough B, Labby ZE, Frigo SP. Portability of IMRT QA between matched linear accelerators. J Appl Clin Med Phys. 2024 Sep 9;e14492.
Barraclough, Brendan, et al. “Portability of IMRT QA between matched linear accelerators.J Appl Clin Med Phys, Sept. 2024, p. e14492. Pubmed, doi:10.1002/acm2.14492.
Barraclough B, Labby ZE, Frigo SP. Portability of IMRT QA between matched linear accelerators. J Appl Clin Med Phys. 2024 Sep 9;e14492.

Published In

J Appl Clin Med Phys

DOI

EISSN

1526-9914

Publication Date

September 9, 2024

Start / End Page

e14492

Location

United States

Related Subject Headings

  • Nuclear Medicine & Medical Imaging
  • 5105 Medical and biological physics
  • 3208 Medical physiology
  • 1116 Medical Physiology
  • 1103 Clinical Sciences
  • 0299 Other Physical Sciences