Lack of repeatability of radiomic features derived from PET scans: Results from a 18F‐DCFPyL test–retest cohort

Author:

Werner Rudolf A.12,Habacha Bilêl3,Lütje Susanne3,Bundschuh Lena4,Kosmala Alekandser1,Essler Markus3,Derlin Thorsten5ORCID,Higuchi Takahiro1,Lapa Constantin4,Buck Andreas K.1,Pienta Kenneth J.6,Lodge Martin A.2,Eisenberger Mario A.7,Markowski Mark C.7ORCID,Pomper Martin G.267,Gorin Michael A.8,Frey Eric C.9,Rowe Steven P.267ORCID,Bundschuh Ralph A.34ORCID

Affiliation:

1. Department of Nuclear Medicine University Hospital Würzburg Würzburg Germany

2. The Russell H. Morgan Department of Radiology and Radiological Science Johns Hopkins University School of Medicine Baltimore Maryland USA

3. Department of Nuclear Medicine University Hospital Bonn Bonn Germany

4. Nuclear Medicine, Medical Faculty University of Augsburg Augsburg Germany

5. Department of Nuclear Medicine Hannover Medical School Hannover Germany

6. Department of Urology, The James Buchanan Brady Urological Institute Johns Hopkins University School of Medicine Baltimore Maryland USA

7. Johns Hopkins University School of Medicine Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland USA

8. Milton and Carroll Petrie Department of Urology Icahn School of Medicine at Mount Sinai New York New York USA

9. Radiopharmaceutical Imaging and Dosimetry, LLC Baltimore Maryland USA

Abstract

AbstractObjectivesPET‐based radiomic metrics are increasingly utilized as predictive image biomarkers. However, the repeatability of radiomic features on PET has not been assessed in a test–retest setting. The prostate‐specific membrane antigen‐targeted compound 18F‐DCFPyL is a high‐affinity, high‐contrast PET agent that we utilized in a test‐retest cohort of men with metastatic prostate cancer (PC).MethodsData of 21 patients enrolled in a prospective clinical trial with histologically proven PC underwent two 18F‐DCFPyL PET scans within 7 days, using identical acquisition and reconstruction parameters. Sites of disease were segmented and a set of 29 different radiomic parameters were assessed on both scans. We determined repeatability of quantification by using Pearson's correlations, within‐subject coefficient of variation (wCOV), and Bland–Altman analysis.ResultsIn total, 230 lesions (177 bone, 38 lymph nodes, 15 others) were assessed on both scans. For all investigated radiomic features, a broad range of inter‐scan correlation was found (r, 0.07–0.95), with acceptable reproducibility for entropy and homogeneity (wCOV, 16.0% and 12.7%, respectively). On Bland–Altman analysis, no systematic increase or decrease between the scans was observed for either parameter (±1.96 SD: 1.07/−1.30, 0.23/−0.18, respectively). The remaining 27 tested radiomic metrics, however, achieved unacceptable high wCOV (≥21.7%).ConclusionMany common radiomic features derived from a test–retest PET study had poor repeatability. Only Entropy and homogeneity achieved good repeatability, supporting the notion that those image biomarkers may be incorporated in future clinical trials. Those radiomic features based on high frequency aspects of images appear to lack the repeatability on PET to justify further study.

Publisher

Wiley

Subject

Urology,Oncology

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