Association of lung fluorodeoxyglucose uptake with radiation pneumonitis after concurrent chemoradiation for non-small cell lung cancer. (June 2017)
- Record Type:
- Journal Article
- Title:
- Association of lung fluorodeoxyglucose uptake with radiation pneumonitis after concurrent chemoradiation for non-small cell lung cancer. (June 2017)
- Main Title:
- Association of lung fluorodeoxyglucose uptake with radiation pneumonitis after concurrent chemoradiation for non-small cell lung cancer
- Authors:
- Yue, Jinbo
McKeever, Matthew
Sio, Terence T.
Xu, Ting
Huo, Jinhai
Shi, Qiuling
Nguyen, Quynh-Nhu
Komaki, Ritsuko
Gomez, Daniel R.
Pan, Tinsu
Wang, Xin Shelley
Liao, Zhongxing - Abstract:
- Abstract: Background: Increased uptake of fluorodeoxyglucose (FDG) by lung tissue could reflect inflammatory changes related to radiation pneumonitis (RP). In this secondary analysis of a clinical trial, we examined potential associations between posttreatment lung FDG uptake and RP severity in patients with non-small cell lung cancer (NSCLC) for up to 12 months after concurrent chemoradiation (CRT). Methods: Subjects were 152 patients with NSCLC who had received concurrent CRT as part of the prospective trial NCT00915005. The following lung FDG variables were evaluated after CRT: maximum, mean, and peak standardized uptake values (SUVmax, SUVmean, SUVpeak) and global lung glycolysis (GLG; lung SUVmean × lung volume). RP severity was scored with the Common Terminology Criteria for Adverse Events v3.0. Results: Significant associations were noted between PET findings and RP severity at 1–6 months (all P < 0.05), but not at 7–12 months after therapy (all P > 0.05). Lung FDG uptake at 1–3 months after treatment predicted later development of grade ≥2 RP (all P < 0.05), with cutoff values as follows: 4.54 for SUVmax, 3.69 for SUVpeak, 0.78 for SUVmean, and 2295 for GLG. Conclusions: Lung FDG uptake correlated significantly with RP severity during the first 6 months after CRT. The cutoff values seem clinically meaningful for identifying patients at risk of developing RP after such therapy.
- Is Part Of:
- Clinical and translational radiation oncology. Volume 4(2017)
- Journal:
- Clinical and translational radiation oncology
- Issue:
- Volume 4(2017)
- Issue Display:
- Volume 4, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 4
- Issue:
- 2017
- Issue Sort Value:
- 2017-0004-2017-0000
- Page Start:
- 1
- Page End:
- 7
- Publication Date:
- 2017-06
- Subjects:
- FDG PET -- Radiation pneumonitis -- Clinician-rated toxicity -- Non-small cell lung cancer -- Radiotherapy
Cancer -- Radiotherapy -- Periodicals
Oncology -- Periodicals
Cancer -- Radiotherapy
Oncology
Radiation Oncology
Neoplasms -- radiotherapy
Translational Medical Research
Periodicals
Electronic journals
Periodicals
616.9940642 - Journal URLs:
- https://www.journals.elsevier.com/clinical-and-translational-radiation-oncology ↗
http://www.sciencedirect.com/science/journal/24056308 ↗
http://www.sciencedirect.com/ ↗ - DOI:
- 10.1016/j.ctro.2017.04.001 ↗
- Languages:
- English
- ISSNs:
- 2405-6308
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - BLDSS-3PM
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