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Establishing the feasibility of the dosimetric compliance criteria of RTOG 1308: phase III randomized trial comparing overall survival after photon versus proton radiochemotherapy for inoperable stage II-IIIB NSCLC

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Last modified
  • 05/15/2025
Type of Material
Authors
    Tawfik Giaddui, Thomas Jefferson UniversityWenzhou Chen, Thomas Jefferson UniversityJialu Yu, Thomas Jefferson UniversityLiyong Lin, Emory UniversityCharles B. Simone, University of PennsylvaniaLulin Yuan, Duke UniversityYutao U. T. Gong, Thomas Jefferson UniversityQ. Jackie Wu, Duke UniversityRadhe Mohan, MD Anderson Cancer CenterXiaodong Zhang, Emory UniversityJaques B. Bluett, MD Anderson Cancer CenterMichael Gillin, MD Anderson Cancer CenterKevin Moore, University of California San DiegoElizabeth O'Meara, Imaging & Radiat Oncol Core IROC Philadelphia RTJennifer Presley, Imaging & Radiat Oncol Core IROC Philadelphia RTJeffrey D. Bradley, Washington UniversityZhongxing Liao, MD Anderson Cancer CenterJames Galvin, Imaging and Radiation Oncology CoreYing Xiao, University of Pennsylvania
Language
  • English
Date
  • 2016-05-04
Publisher
  • BMC (part of Springer Nature)
Publication Version
Copyright Statement
  • © 2016 Giaddui et al.
License
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 1748-717X
Volume
  • 11
Issue
  • 1
Start Page
  • 66
End Page
  • 66
Grant/Funding Information
  • This project was supported by grants U10CA180868, U10CA180822 and U24CA180803 and U24 RFA-CA-12-014 from the National Cancer Institute (NCI) and the Cure Grant from the Department of Health in Pennsylvania.
Abstract
  • Background: To establish the feasibility of the dosimetric compliance criteria of the RTOG 1308 trial through testing against Intensity Modulation Radiation Therapy (IMRT) and Passive Scattering Proton Therapy (PSPT) plans. Methods: Twenty-six lung IMRT and 26 proton PSPT plans were included in the study. Dose Volume Histograms (DVHs) for targets and normal structures were analyzed. The quality of IMRT plans was assessed using a knowledge-based engineering tool. Results: Most of the RTOG 1308 dosimetric criteria were achieved. The deviation unacceptable rates were less than 10 % for most criteria; however, a deviation unacceptable rate of more than 20 % was computed for the planning target volume minimum dose compliance criterion. Dose parameters for the target volume were very close for the IMRT and PSPT plans. However, the PSPT plans led to lower dose values for normal structures. The dose parameters in which PSPT plans resulted in lower values than IMRT plans were: lung V5Gy(%) (34.4 in PSPT and 47.2 in IMRT); maximum spinal cord dose (31.7 Gy in PSPT and 43.5 Gy in IMRT); heart V5Gy(%) (19 in PSPT and 47 in IMRT); heart V30Gy(%) (11 in PSPT and 19 in IMRT); heart V45Gy(%) (7.8 in PSPT and 12.1 in IMRT); heart V50%(Gy) (7.1 in PSPT and 9.8 in IMRT) and mean heart dose (7.7 Gy in PSPT and 14.9 Gy in IMRT). Conclusions: The revised RTOG 1308 dosimetric compliance criteria are feasible and achievable.
Author Notes
Keywords
Research Categories
  • Health Sciences, Radiology
  • Health Sciences, Oncology

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