Inverse Verification of the Dose Distribution for Intensity Modulated Radiation Therapy Patient-specific Quality Assurance Using Dynamic MLC Log Files

被引:7
|
作者
Lee, Jeong-Woo [1 ,2 ]
Park, Jeong-Hoon [1 ]
Chung, Jin-Beom [1 ]
Park, Ji-Yeon [1 ]
Choe, Bo-Young [1 ]
Suh, Tae-Suk [1 ]
Lee, Doo-Hyun [1 ,3 ]
Hong, Semie [2 ]
Kang, Min-Young [2 ]
Choi, Kyoung-Sik [4 ]
机构
[1] Catholic Univ Korea, Res Inst Biomed Engn, Dept Biomed Engn, Seoul 137701, South Korea
[2] Konkuk Univ, Med Ctr, Dept Radiat Oncol, Seoul 143729, South Korea
[3] Natl Canc Ctr, Dept Radiat Oncol, Goyang 410769, South Korea
[4] Sam Med Ctr, Dept Radiat Oncol, Anyang 430733, South Korea
关键词
IMRT patient-specific QA; Dynamic MLC log file; DVH; Gamma index; QUANTITATIVE-EVALUATION; IMRT; DELIVERY; RADIOTHERAPY; DOCUMENT;
D O I
10.3938/jkps.55.1649
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
The aim of this study was to investigate a novel method for verification of the close distribution for intensity modulated radiation therapy (IMRT) patient-specific quality assurance (QA) using dynamic multi-leaf collimator (DMLC) log files (Dynalog files). Dynalog files are recorded every 50 ms by using a MLC controller during the IMRT treatment. Dynalog files contain actual MLC positional information for various delivered dose fractions. As the nonuniform fluence is directly influenced by the MLC positional accuracy, our method for IMRT patient-specific QA can be performed using this information. Three nasopharyugeal cancer patients were selected for the evaluation. We developed an in-house program to convert MLC log files from an MLC controller to delivered MLC (dMLC) field files for the interface between the MLC controller and the treatment planning system. The in-house software, DMLC field file (DFF) converter, was written using programming language (Visual C++ 2005, Microsoft, Redmond, WA, USA). For inverse planning, Eclipse (v. 6.5, Varian, Palo Alto, USA) was used. The MLC log files were converted to dMLC files. The IMRT plans were recalculated and compared with the original plans. Comparisons were done via planar dose distributions using OP-IMRT software (v. 1.4, Wellhofer Dosimetric, Germany) and dose volume histograms (DVHs) for targets and organs at risk (OARs). Gamma index (dose difference: 3%, distance to agreement: 3 mm) calculations were also performed for a quantitative analysis. There were significant differences (maximum dose difference: 587 cGy, maximum volume difference at 3000 cGy: 17%) in the DVHs of the parotid glands between planned MLC (pMLC)-based and delivered MLC (dMLC)-based inverse IMRT QA (IVQA) plans for all three patients. The histograms showed an increased dose-volume in the dMLC-based IVQA deliveries compared to reference (Ref.) IMRT plans. Based on the present study, we can confirm the availability of our new approach to perform IMRT patient-specific QA providing a convenient and clear tool for IMRT dose verification. In the future, this method should be available for inverse on-treatment close verification and for pre-treatment IMRT QA.
引用
收藏
页码:1649 / 1656
页数:8
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