Multisite Technical and Clinical Performance Evaluation of Quantitative Imaging Biomarkers from 3D FDG PET Segmentations of Head and Neck Cancer Images.

TitleMultisite Technical and Clinical Performance Evaluation of Quantitative Imaging Biomarkers from 3D FDG PET Segmentations of Head and Neck Cancer Images.
Publication TypeJournal Article
Year of Publication2020
AuthorsSmith BJ, Buatti JM, Bauer C, Ulrich EJ, Ahmadvand P, Budzevich MM, Gillies RJ, Goldgof D, Grkovski M, Hamarneh G, Kinahan PE, Muzi JP, Muzi M, Laymon CM, Mountz JM, Nehmeh S, Oborski MJ, Zhao B, Sunderland JJ, Beichel RR
JournalTomography
Volume6
Issue2
Pagination65-76
Date Published2020 06
ISSN2379-139X
KeywordsBayes Theorem, Biomarkers, Tumor, Fluorodeoxyglucose F18, Head and Neck Neoplasms, Humans, Positron-Emission Tomography, Reproducibility of Results, Tomography, X-Ray Computed
Abstract

Quantitative imaging biomarkers (QIBs) provide medical image-derived intensity, texture, shape, and size features that may help characterize cancerous tumors and predict clinical outcomes. Successful clinical translation of QIBs depends on the robustness of their measurements. Biomarkers derived from positron emission tomography images are prone to measurement errors owing to differences in image processing factors such as the tumor segmentation method used to define volumes of interest over which to calculate QIBs. We illustrate a new Bayesian statistical approach to characterize the robustness of QIBs to different processing factors. Study data consist of 22 QIBs measured on 47 head and neck tumors in 10 positron emission tomography/computed tomography scans segmented manually and with semiautomated methods used by 7 institutional members of the NCI Quantitative Imaging Network. QIB performance is estimated and compared across institutions with respect to measurement errors and power to recover statistical associations with clinical outcomes. Analysis findings summarize the performance impact of different segmentation methods used by Quantitative Imaging Network members. Robustness of some advanced biomarkers was found to be similar to conventional markers, such as maximum standardized uptake value. Such similarities support current pursuits to better characterize disease and predict outcomes by developing QIBs that use more imaging information and are robust to different processing factors. Nevertheless, to ensure reproducibility of QIB measurements and measures of association with clinical outcomes, errors owing to segmentation methods need to be reduced.

DOI10.18383/j.tom.2020.00004
Alternate JournalTomography
PubMed ID32548282
PubMed Central IDPMC7289247
Grant ListU24 CA180918 / CA / NCI NIH HHS / United States
UL1 TR002537 / TR / NCATS NIH HHS / United States
U01 CA140206 / CA / NCI NIH HHS / United States
P30 CA086862 / CA / NCI NIH HHS / United States
R50 CA211270 / CA / NCI NIH HHS / United States
U01 CA148131 / CA / NCI NIH HHS / United States
P30 CA008748 / CA / NCI NIH HHS / United States
R01 EB004640 / EB / NIBIB NIH HHS / United States

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065