| Radiation Oncology | |
| Evaluation of heterogeneity dose distributions for Stereotactic Radiotherapy (SRT): comparison of commercially available Monte Carlo dose calculation with other algorithms | |
| Keiichi Nakagawa1  Akihiro Haga1  Akira Sakumi1  Yoshio Iwai2  Naoya Saotome1  Hideomi Yamashita1  Wataru Takahashi1  | |
| [1] Department of Radiology, University of Tokyo Hospital, Hongo, Bunkyo-ku, Tokyo, Japan;Elekta KK, 3-9-1 Shibaura, Minato-ku, Tokyo 108-0023, Japan | |
| 关键词: Tissue inhomogeneities; Lung cancer; Stereotactic body radiotherapy (SBRT); Calculation algorithm; Monte Carlo; | |
| Others : 1160896 DOI : 10.1186/1748-717X-7-20 |
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| received in 2011-09-12, accepted in 2012-02-09, 发布年份 2012 | |
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【 摘 要 】
Background
The purpose of this study was to compare dose distributions from three different algorithms with the x-ray Voxel Monte Carlo (XVMC) calculations, in actual computed tomography (CT) scans for use in stereotactic radiotherapy (SRT) of small lung cancers.
Methods
Slow CT scan of 20 patients was performed and the internal target volume (ITV) was delineated on Pinnacle3. All plans were first calculated with a scatter homogeneous mode (SHM) which is compatible with Clarkson algorithm using Pinnacle3 treatment planning system (TPS). The planned dose was 48 Gy in 4 fractions. In a second step, the CT images, structures and beam data were exported to other treatment planning systems (TPSs). Collapsed cone convolution (CCC) from Pinnacle3, superposition (SP) from XiO, and XVMC from Monaco were used for recalculating. The dose distributions and the Dose Volume Histograms (DVHs) were compared with each other.
Results
The phantom test revealed that all algorithms could reproduce the measured data within 1% except for the SHM with inhomogeneous phantom. For the patient study, the SHM greatly overestimated the isocenter (IC) doses and the minimal dose received by 95% of the PTV (PTV95) compared to XVMC. The differences in mean doses were 2.96 Gy (6.17%) for IC and 5.02 Gy (11.18%) for PTV95. The DVH's and dose distributions with CCC and SP were in agreement with those obtained by XVMC. The average differences in IC doses between CCC and XVMC, and SP and XVMC were -1.14% (p = 0.17), and -2.67% (p = 0.0036), respectively.
Conclusions
Our work clearly confirms that the actual practice of relying solely on a Clarkson algorithm may be inappropriate for SRT planning. Meanwhile, CCC and SP were close to XVMC simulations and actual dose distributions obtained in lung SRT.
【 授权许可】
2012 Takahashi et al; licensee BioMed Central Ltd.
【 预 览 】
| Files | Size | Format | View |
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| 20150411083438163.pdf | 1385KB | ||
| Figure 5. | 34KB | Image | |
| Figure 4. | 22KB | Image | |
| Figure 3. | 34KB | Image | |
| Figure 2. | 42KB | Image | |
| Figure 1. | 44KB | Image |
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