Institutional Patient-specific IMRT QA Does Not Predict Unacceptable Plan Delivery

Purpose To determine whether in-house patient-specific intensity modulated radiation therapy quality assurance (IMRT QA) results predict Imaging and Radiation Oncology Core (IROC)-Houston phantom results. Methods and Materials IROC Houston's IMRT head and neck phantoms have been irradiated by n...

Full description

Saved in:
Bibliographic Details
Published inInternational journal of radiation oncology, biology, physics Vol. 90; no. 5; pp. 1195 - 1201
Main Authors Kry, Stephen F., PhD, Molineu, Andrea, MS, Kerns, James R., MS, Faught, Austin M., PhD, Huang, Jessie Y., BS, Pulliam, Kiley B., MS, Tonigan, Jackie, MS, Alvarez, Paola, MS, Stingo, Francesco, PhD, Followill, David S., PhD
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 01.12.2014
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Purpose To determine whether in-house patient-specific intensity modulated radiation therapy quality assurance (IMRT QA) results predict Imaging and Radiation Oncology Core (IROC)-Houston phantom results. Methods and Materials IROC Houston's IMRT head and neck phantoms have been irradiated by numerous institutions as part of clinical trial credentialing. We retrospectively compared these phantom results with those of in-house IMRT QA (following the institution's clinical process) for 855 irradiations performed between 2003 and 2013. The sensitivity and specificity of IMRT QA to detect unacceptable or acceptable plans were determined relative to the IROC Houston phantom results. Additional analyses evaluated specific IMRT QA dosimeters and analysis methods. Results IMRT QA universally showed poor sensitivity relative to the head and neck phantom, that is, poor ability to predict a failing IROC Houston phantom result. Depending on how the IMRT QA results were interpreted, overall sensitivity ranged from 2% to 18%. For different IMRT QA methods, sensitivity ranged from 3% to 54%. Although the observed sensitivity was particularly poor at clinical thresholds (eg 3% dose difference or 90% of pixels passing gamma), receiver operator characteristic analysis indicated that no threshold showed good sensitivity and specificity for the devices evaluated. Conclusions IMRT QA is not a reasonable replacement for a credentialing phantom. Moreover, the particularly poor agreement between IMRT QA and the IROC Houston phantoms highlights surprising inconsistency in the QA process.
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ISSN:0360-3016
1879-355X
DOI:10.1016/j.ijrobp.2014.08.334