AAPM Task Group Report 307: Use of EPIDs for Patient‐Specific IMRT and VMAT QA

Author:

Dogan Nesrin1,Mijnheer Ben J.2,Padgett Kyle1,Nalichowski Adrian3,Wu Chuan4,Nyflot Matthew J.5,Olch Arthur J.6,Papanikolaou Niko7,Shi Jie8,Holmes Shannon M.9,Moran Jean10,Greer Peter B.1112

Affiliation:

1. Department of Radiation Oncology University of Miami Miller School of Medicine Miami Florida USA

2. Department of Radiation Oncology Netherlands Cancer Institute Amsterdam Netherlands

3. Department of Radiation Oncology Karmanos Cancer Institute Detroit Michigan USA

4. Department of Radiation Oncology Sutter Medical Foundation Roseville California USA

5. Department of Radiation Oncology University of Washington Seattle Washington USA

6. Department of Radiation Oncology University of Southern California, and Children's Hospital Los Angeles Los Angeles California USA

7. Division of Medical Physics UT Health‐MD Anderson San Antonio Texas USA

8. Sun Nuclear Corporation – A Mirion Medical Company Melbourne Florida USA

9. Standard Imaging, Inc. Middleton Wisconsin USA

10. Department of Medical Physics Memorial Sloan Kettering Cancer Center New York New York USA

11. Department of Radiation Oncology Calvary Mater Newcastle Hospital Newcastle NSW Australia

12. School of Information and Physical Sciences University of Newcastle Newcastle NSW Australia

Abstract

AbstractPurposeElectronic portal imaging devices (EPIDs) have been widely utilized for patient‐specific quality assurance (PSQA) and their use for transit dosimetry applications is emerging. Yet there are no specific guidelines on the potential uses, limitations, and correct utilization of EPIDs for these purposes. The American Association of Physicists in Medicine (AAPM) Task Group 307 (TG‐307) provides a comprehensive review of the physics, modeling, algorithms and clinical experience with EPID‐based pre‐treatment and transit dosimetry techniques. This review also includes the limitations and challenges in the clinical implementation of EPIDs, including recommendations for commissioning, calibration and validation, routine QA, tolerance levels for gamma analysis and risk‐based analysis.MethodsCharacteristics of the currently available EPID systems and EPID‐based PSQA techniques are reviewed. The details of the physics, modeling, and algorithms for both pre‐treatment and transit dosimetry methods are discussed, including clinical experience with different EPID dosimetry systems. Commissioning, calibration, and validation, tolerance levels and recommended tests, are reviewed, and analyzed. Risk‐based analysis for EPID dosimetry is also addressed.ResultsClinical experience, commissioning methods and tolerances for EPID‐based PSQA system are described for pre‐treatment and transit dosimetry applications. The sensitivity, specificity, and clinical results for EPID dosimetry techniques are presented as well as examples of patient‐related and machine‐related error detection by these dosimetry solutions. Limitations and challenges in clinical implementation of EPIDs for dosimetric purposes are discussed and acceptance and rejection criteria are outlined. Potential causes of and evaluations of pre‐treatment and transit dosimetry failures are discussed. Guidelines and recommendations developed in this report are based on the extensive published data on EPID QA along with the clinical experience of the TG‐307 members.ConclusionTG‐307 focused on the commercially available EPID‐based dosimetric tools and provides guidance for medical physicists in the clinical implementation of EPID‐based patient‐specific pre‐treatment and transit dosimetry QA solutions including intensity modulated radiation therapy (IMRT) and volumetric modulated arc therapy (VMAT) treatments.

Publisher

Wiley

Subject

General Medicine

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