2015
DOI: 10.1016/j.ejmp.2015.05.001
|View full text |Cite
|
Sign up to set email alerts
|

Film-based delivery quality assurance for robotic radiosurgery: Commissioning and validation

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
3
1
1

Citation Types

5
54
0

Year Published

2016
2016
2023
2023

Publication Types

Select...
7

Relationship

1
6

Authors

Journals

citations
Cited by 33 publications
(59 citation statements)
references
References 27 publications
5
54
0
Order By: Relevance
“…The commissioning and validation for film based CyberKnife DQA using various test scenarios [7] was recently reported and results confirmed that, by means of accurate film-to-plan registration, maximum Gamma-Index pass-rate search and tight distance-to-agreement (DTA) criteria, small errors in beam delivery and system miscalibration can be detected. However, some drawbacks of film based methods applied to CyberKnife, remained unsolved: (1) absolute film dosimetry requires additional ion-chamber verification and appears to have an accuracy of no less than 3% [7] and (2) film DQA evaluation is cumbersome and requires long wait times (up to several hours) after irradiation. The generally long times required both to perform and analyze patient specific film DQA may significantly reduce the number of dosimetrically verified clinical treatment plans.…”
Section: Introductionsupporting
confidence: 55%
See 1 more Smart Citation
“…The commissioning and validation for film based CyberKnife DQA using various test scenarios [7] was recently reported and results confirmed that, by means of accurate film-to-plan registration, maximum Gamma-Index pass-rate search and tight distance-to-agreement (DTA) criteria, small errors in beam delivery and system miscalibration can be detected. However, some drawbacks of film based methods applied to CyberKnife, remained unsolved: (1) absolute film dosimetry requires additional ion-chamber verification and appears to have an accuracy of no less than 3% [7] and (2) film DQA evaluation is cumbersome and requires long wait times (up to several hours) after irradiation. The generally long times required both to perform and analyze patient specific film DQA may significantly reduce the number of dosimetrically verified clinical treatment plans.…”
Section: Introductionsupporting
confidence: 55%
“…Radiochromic film measurement is the current method of choice both for routine QA as well as specific validation of patient treatment plans for the CyberKnife [6,7]. The commissioning and validation for film based CyberKnife DQA using various test scenarios [7] was recently reported and results confirmed that, by means of accurate film-to-plan registration, maximum Gamma-Index pass-rate search and tight distance-to-agreement (DTA) criteria, small errors in beam delivery and system miscalibration can be detected.…”
Section: Introductionmentioning
confidence: 99%
“…Gamma‐index analysis 20 was used to compare the measurements and calculations, by applying a criterion of 3% local pixel dose difference (LPDD)/2 mm distance‐to‐agreement (DTA) and a threshold of 30% of the maximum dose. This criterion was determined based on previous studies,21, 22, 23 and the threshold was set according to the dose constraints of the critical organs.…”
Section: Methodsmentioning
confidence: 99%
“…[11][12][13] 2D film dosimetry offers superior spatial resolution for small field measurements, but the resulting dose distributions are sensi- The CyberKnife system has a predefined safety zone around the patient based on the patient's size. When we perform the patient-specific QA for a patient with the brain tumor, special attention is required to avoid the collision between the patient-specific QA phantom including Octavius 1000SRS detector and the moving robot arm due to the narrow patient safety zone.…”
Section: Discussionmentioning
confidence: 99%