Abstract
Objectives
Radiomic involves testing the associations of a large number of quantitative imaging features with clinical characteristics. Our aim was to extract a radiomic signature from axial T2-weighted (T2-W) magnetic resonance imaging (MRI) of the whole prostate able to predict oncological and radiological scores in prostate cancer (PCa).
Methods
This study included 65 patients with localized PCa treated with radiotherapy (RT) between 2014 and 2018. For each patient, the T2-W MRI images were normalized with the histogram intensity scale standardization method. Features were extracted with the IBEX software. The association of each radiomic feature with risk class, T-stage, Gleason score (GS), extracapsular extension (ECE) score, and Prostate Imaging Reporting and Data System (PI-RADS v2) score was assessed by univariate and multivariate analysis.
Results
Forty-nine out of 65 patients were eligible. Among the 1702 features extracted, 3 to 6 features with the highest predictive power were selected for each outcome. This analysis showed that texture features were the most predictive for GS, PI-RADS v2 score, and risk class; intensity features were highly associated with T-stage, ECE score, and risk class, with areas under the receiver operating characteristic curve (ROC AUC) ranging from 0.74 to 0.94.
Conclusions
MRI-based radiomics is a promising tool for prediction of PCa characteristics. Although a significant association was found between the selected features and all the mentioned clinical/radiological scores, further validations on larger cohorts are needed before these findings can be applied in the clinical practice.
Key Points
• A radiomic model was used to classify PCa aggressiveness.
• Radiomic analysis was performed on T2-W magnetic resonance images of the whole prostate gland.
• The most predictive features belong to the texture (57%) and intensity (43%) domains.
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Abbreviations
- ADC:
-
Apparent diffusion coefficient
- AIRC:
-
Associazione Italiana per la Ricerca sul Cancro
- AS:
-
Active surveillance
- AUC:
-
Area under the curve
- CI:
-
Confidence intervals
- DCE:
-
Dynamic contrast-enhanced
- DIL:
-
Dominant intraprostatic lesion
- DWI:
-
Diffusion-weighted imaging
- EBRT:
-
External beam radiotherapy
- ECE:
-
Extracapsular extension
- FDR:
-
False discovery rate
- Gb-scale:
-
Generalized ball scale
- GLCM:
-
Gray-level co-occurrence matrix
- GLRLM:
-
Gray-level run length matrix
- GOH:
-
Gradient orient histogram
- GS:
-
Gleason score
- G-scale:
-
Generalized scale
- IH:
-
Intensity histogram
- HT:
-
Hormone therapy
- ID:
-
Intensity direct
- IMRT-SIB:
-
Intensity-modulated radiation therapy simultaneous integrated boost
- ISUP:
-
International Society of Urological Pathology
- KW:
-
Kruskal-Wallis
- mpMRI:
-
Multiparametric magnetic resonance imaging
- NCCN:
-
National Comprehensive Cancer Network
- NID:
-
Neighborhood intensity difference
- PC:
-
Custom normalization based on healthy tissue intensities in the prostate
- PCa:
-
Prostate cancer
- PI-RADS:
-
Prostate imaging reporting and data system
- PROMIS:
-
Prostate mr imaging study
- PROTECT:
-
Prostate testing for cancer and treatment
- PSA:
-
Prostate-specific antigen
- PTEN:
-
Phosphatase and tensin homolog
- ROC:
-
Receiver operating characteristics
- ROI:
-
Regions of interest
- RP:
-
Prostatectomy
- RT:
-
Radiotherapy
- T2-W:
-
T2-weighted
- VOI:
-
Volume of interest
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Acknowledgments
LJI was partially supported by Associazione Italiana per la Ricerca sul Cancro (AIRC), by project IG-13218 “Short-term High Precision Radiotherapy for Early Prostate Cancer With Concomitant Boost on the Dominant Lesion,” registered at ClinicalTrials.gov (NCT01913717), and SGG by project IG-14300 “Carbon ions boost followed by pelvic photon intensity modulated radiotherapy for high-risk prostate cancer,” registered at ClinicalTrials.gov (NCT02672449). MP was supported by a research grant from Accuray Inc. entitled “Data collection and analysis of Tomotherapy and CyberKnife breast clinical studies, breast physics studies and prostate study.” The work was also partially supported by the Italian Ministry of Health with Ricerca Corrente and 5x1000 funds. The sponsors did not play any role in the study design, collection, analysis and interpretation of data, nor in the writing of the manuscript, nor in the decision to submit the manuscript for publication. All authors have participated in (a) conception and design, or analysis and interpretation of the data; (b) drafting the article or revising it critically for important intellectual content; and (c) approval of the final version.
This manuscript has not been submitted to, nor is under review at, another journal or other publishing venue.
Funding
The study was partially funded by Associazione Italiana per la Ricerca sul Cancro (AIRC) and by Accuray Inc.
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The scientific guarantor of this publication is Prof. Barbara Alicja Jereczek-Fossa.
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The authors of this manuscript declare no relationships with any companies, whose products or services may be related to the subject matter of the article.
Statistics and biometry
Two of the authors are biostatisticians.
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Written informed consent was obtained from all patients in this study.
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Institutional Review Board approval was obtained.
Methodology
• Retrospective
• Experimental
• Study performed at one institution
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The first affiliation was the affiliation at the time of data collection for authors Simone Giovanni Gugliandolo, Delia Ciardo and Giulia Riva.
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Gugliandolo, S.G., Pepa, M., Isaksson, L.J. et al. MRI-based radiomics signature for localized prostate cancer: a new clinical tool for cancer aggressiveness prediction? Sub-study of prospective phase II trial on ultra-hypofractionated radiotherapy (AIRC IG-13218). Eur Radiol 31, 716–728 (2021). https://doi.org/10.1007/s00330-020-07105-z
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DOI: https://doi.org/10.1007/s00330-020-07105-z