Kazuki Kubo1,2, Hajime Monzen1, Kohei Shimomura3, Kenji Matsumoto4, Tomoharu Sato5, Mikoto Tamura1,4, Kiyoshi Nakamatsu6, Kentaro Ishii2, Ryu Kawamorita2. 1. Department of Medical Physics, Graduate School of Medical Sciences, Kindai University, 377-2 Ohno-higashi, Osaka-sayama-shi, Osaka 589-8511, Japan. 2. Department of Radiation Oncology, Tane General Hospital, 1-12-21 Kujo-minami, Nishi-Ku Osaka-shi, Osaka 550-0025, Japan. 3. Department of Radiological Technology, Faculty of Medical Science, Kyoto College of Medical Science, 1-3 Imakita Sonobe-cho Oyama-higashi-machi, Nantan-shi, Kyoto 622-0041, Japan. 4. Department of Central Radiology, Kindai University Hospital, 377-2 Ohno-higashi, Osaka-sayama-shi, Osaka 589-8511, Japan. 5. Department of Radiation Oncology, Cancer Institute Hospital, 3-8-31, Ariake, Koto, Tokyo 135-8550, Japan. 6. Department of Radiation Oncology, Kindai University, 377-2 Ohno-higashi, Osaka-sayama-shi, Osaka 589-8511, Japan.
Abstract
AIM: To evaluate the success of a patient-specific intensity modulated radiation therapy (IMRT) quality assurance (QA) practice for prostate cancer patients across multiple institutions using a questionnaire survey. BACKGROUND: The IMRT QA practice involves different methods of dose distribution verification and analysis at different institutions. MATERIALS AND METHODS: Two full-arc volumetric modulated arc therapy (VMAT) plan and 7 fixed-gantry IMRT plan with DMLC were used for patient specific QA across 22 institutions. The same computed tomography image and structure set were used for all plans. Each institution recalculated the dose distribution with fixed monitor units and without any modification. Single-point dose measurement with a cylindrical ionization chamber and dose distribution verification with a multi-detector or radiochromic film were performed, according to the QA process at each institution. RESULTS: Twenty-two institutions performed the patient-specific IMRT QA verifications. With a single-point dose measurement at the isocenter, the average difference between the calculated and measured doses was 0.5 ± 1.9%. For the comparison of dose distributions, 18 institutions used a two or three-dimensional array detector, while the others used Gafchromic film. In the γ test with dose difference/distance-to-agreement criteria of 3%-3 mm and 2%-2 mm with a 30% dose threshold, the median gamma pass rates were 99.3% (range: 41.7%-100.0%) and 96.4% (range: 29.4%-100.0%), respectively. CONCLUSION: This survey was an informative trial to understand the verification status of patient-specific IMRT QA measurements for prostate cancer. In most institutions, the point dose measurement and dose distribution differences met the desired criteria.
AIM: To evaluate the success of a patient-specific intensity modulated radiation therapy (IMRT) quality assurance (QA) practice for prostate cancer patients across multiple institutions using a questionnaire survey. BACKGROUND: The IMRT QA practice involves different methods of dose distribution verification and analysis at different institutions. MATERIALS AND METHODS: Two full-arc volumetric modulated arc therapy (VMAT) plan and 7 fixed-gantry IMRT plan with DMLC were used for patient specific QA across 22 institutions. The same computed tomography image and structure set were used for all plans. Each institution recalculated the dose distribution with fixed monitor units and without any modification. Single-point dose measurement with a cylindrical ionization chamber and dose distribution verification with a multi-detector or radiochromic film were performed, according to the QA process at each institution. RESULTS: Twenty-two institutions performed the patient-specific IMRT QA verifications. With a single-point dose measurement at the isocenter, the average difference between the calculated and measured doses was 0.5 ± 1.9%. For the comparison of dose distributions, 18 institutions used a two or three-dimensional array detector, while the others used Gafchromic film. In the γ test with dose difference/distance-to-agreement criteria of 3%-3 mm and 2%-2 mm with a 30% dose threshold, the median gamma pass rates were 99.3% (range: 41.7%-100.0%) and 96.4% (range: 29.4%-100.0%), respectively. CONCLUSION: This survey was an informative trial to understand the verification status of patient-specific IMRT QA measurements for prostate cancer. In most institutions, the point dose measurement and dose distribution differences met the desired criteria.
Authors: Moyed Miften; Arthur Olch; Dimitris Mihailidis; Jean Moran; Todd Pawlicki; Andrea Molineu; Harold Li; Krishni Wijesooriya; Jie Shi; Ping Xia; Nikos Papanikolaou; Daniel A Low Journal: Med Phys Date: 2018-03-23 Impact factor: 4.071