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SU-E-T-50: A Multi-Institutional Study of Independent Dose Verification Software Program for Lung SBRT

Journal Article · · Medical Physics
DOI:https://doi.org/10.1118/1.4924411· OSTI ID:22545181
 [1]; ;  [2];  [3]; ;  [4]; ;  [5];  [6];  [7]
  1. Kanagawa Cancer Center, Yokohama, Kanagawa-prefecture (Japan)
  2. The Cancer Institute Hospital of JFCR, Koutou-ku, Tokyo (Japan)
  3. The National Cancer Center Hospital East, Kashiwa-city, Chiba prefecture (Japan)
  4. Otemae Hospital, Chuou-ku, Osaka-city (Japan)
  5. Sasebo City General Hospital, Sasebo, Nagasaki (Japan)
  6. St Lukes International Hospital, Chuou-ku, Tokyo (Japan)
  7. National Cancer Center Hospital East, Kashiwa, Chiba (Japan)
Purpose: The accuracy of dose distribution depends on treatment planning system especially in heterogeneity-region. The tolerance level (TL) of the secondary check using the independent dose verification may be variable in lung SBRT plans. We conducted a multi-institutional study to evaluate the tolerance level of lung SBRT plans shown in the AAPM TG114. Methods: Five institutes in Japan participated in this study. All of the institutes used a same independent dose verification software program (Simple MU Analysis: SMU, Triangle Product, Ishikawa, JP), which is Clarkson-based and CT images were used to compute radiological path length. Analytical Anisotropic Algorithm (AAA), Pencil Beam Convolution with modified Batho-method (PBC-B) and Adaptive Convolve (AC) were used for lung SBRT planning. A measurement using an ion-chamber was performed in a heterogeneous phantom to compare doses from the three different algorithms and the SMU to the measured dose. In addition to it, a retrospective analysis using clinical lung SBRT plans (547 beams from 77 patients) was conducted to evaluate the confidence limit (CL, Average±2SD) in dose between the three algorithms and the SMU. Results: Compared to the measurement, the AAA showed the larger systematic dose error of 2.9±3.2% than PBC-B and AC. The Clarkson-based SMU showed larger error of 5.8±3.8%. The CLs for clinical plans were 7.7±6.0 % (AAA), 5.3±3.3 % (AC), 5.7±3.4 % (PBC -B), respectively. Conclusion: The TLs from the CLs were evaluated. A Clarkson-based system shows a large systematic variation because of inhomogeneous correction. The AAA showed a significant variation. Thus, we must consider the difference of inhomogeneous correction as well as the dependence of dose calculation engine.
OSTI ID:
22545181
Journal Information:
Medical Physics, Journal Name: Medical Physics Journal Issue: 6 Vol. 42; ISSN 0094-2405; ISSN MPHYA6
Country of Publication:
United States
Language:
English