Abstract
Objectives
To assess the potential of radiomic features (RFs) extracted from simulation computed tomography (CT) images in discriminating local progression (LP) after stereotactic body radiotherapy (SBRT) in the management of lung oligometastases (LOM) from colorectal cancer (CRC).
Materials and methods
Thirty-eight patients with 70 LOM treated with SBRT were analyzed. The largest LOM was considered as most representative for each patient and was manually delineated by two blinded radiation oncologists. In all, 141 RFs were extracted from both contours according to IBSI (International Biomarker Standardization Initiative) recommendations. Based on the agreement between the two observers, 134/141 RFs were found to be robust against delineation (intraclass correlation coefficient [ICC] > 0.80); independent RFs were then assessed by Spearman correlation coefficients. The association between RFs and LP was assessed with Mann–Whitney test and univariate logistic regression (ULR): the discriminative power of the most informative RF was quantified by receiver-operating characteristics (ROC) analysis through area under curve (AUC).
Results
In all, 15/38 patients presented LP. Median time to progression was 14.6 months (range 2.4–66 months); 5/141 RFs were significantly associated to LP at ULR analysis (p < 0.05); among them, 4 RFs were selected as robust and independent: Statistical_Variance (AUC = 0.75, p = 0.002), Statistical_Range (AUC = 0.72, p = 0.013), Grey Level Size Zone Matrix (GLSZM) _zoneSizeNonUniformity (AUC = 0.70, p = 0.022), Grey Level Dependence Zone Matrix (GLDZM) _zoneDistanceEntropy (AUC = 0.70, p = 0.026). Importantly, the RF with the best performance (Statisical_Variance) is simply representative of density heterogeneity within LOM.
Conclusion
Four RFs extracted from planning CT were significantly associated with LP of LOM from CRC treated with SBRT. Results encourage further research on a larger population aiming to define a usable radiomic score combining the most predictive RFs and, possibly, additional clinical features.
Similar content being viewed by others
References
Turajlic S, Swanton C (2016) Metastasis as an evolutionary process. Science 352:169–175
Abbosh C, Birkbak NJ, Wilson GA et al (2017) Phylogenetic ctDNA analysis depicts early-stage lung cancer evolution. Nature 545:446–451 (Erratum: Nature, 2018; 554:264)
Turajlic S, Xu H, Litchfield K et al (2018) Tracking cancer evolution reveals constrained routes to metastases: TRACERx renal. Cell 173:581–594.e12
Bartlett EK, Simmons KD, Wachtel H et al (2015) The rise in metastasectomy across cancer types over the past decade. Cancer 121:747–757
Lewis SL, Porceddu S, Nakamura N et al (2017) Definitive stereotactic body radiotherapy (SBRT) for extracranial oligometastases: an international survey of 1000 radiation oncologists. Am J Clin Oncol 40:418–422
Palma DA, Olson R, Harrow S et al (2019) Stereotactic ablative radiotherapy versus standard of care palliative treatment in patients with oligometastatic cancers (SABR-COMET): a randomised, phase 2, open-label trial. Lancet 393:2051–2058
Palma DA, Olson R, Harrow S et al (2020) Stereotactic ablative radiotherapy for the comprehensive treatment of oligometastatic cancers: long-term results of the SABR-COMET phase II randomized trial. J Clin Oncol 38:2830–2838
Zelefsky MJ, Yamada Y, Greco C et al (2021) Phase 3 multi.center, prospective, randomized trial comparing single-dose 24 Gy radiation therapy to a 3-fraction SBRT regimen in the treatment of oligometastatic cancer. Int J Radiat Oncol Biol Phys 110(3):672–679
Sharma A, Duijm M, Oomen-de Hoop E et al (2018) Factors affecting local control of pulmonary oligometastases treated with stereotactic body radiotherapy. Acta Oncol 57(8):1031–1037. https://doi.org/10.1080/0284186X.2018.1445285
Buglione M, Jereczek-Fossa BA, Bonù ML et al (2020) Radiosurgery and fractionated stereotactic radiotherapy in oligometastatic/oligoprogressive non-small cell lung cancer patients: results of a multi-institutional series of 198 patients treated with “curative” intent. Cancer Treat Res 141:1–8
Sheikh S, Chen H, Sahgal A et al (2022) An analysis of a large multi-institutional database reveals important associations between treatment parameters and clinical outcomes for stereotactic body radiotherapy (SBRT) of oligometastatic colorectal cancer. Radiother Oncol 167:187–194
Nicosia L, Franceschini D, Perrone-Congedi F et al (2021) A multicenter LArge retrospectIve daTabase on the personalization of Stereotactic ABlative radiotherapy use in lung metastases from colon-rectal cancer: the laIT-SABR study. Radiother Oncol 166:92–99. https://doi.org/10.1016/j.radonc.2021.10.023
Bezjak A, Paulus R, Gaspar LE et al (2016) Primary study endpoint analysis for NRG oncology/RTOG 0813 trial of Stereotactic body radiation therapy (SBRT) for centrally located non-small cell lung cancer (NSCLC). Int J Radiat Oncol Biol Phys 94(1):5–6
Whybra P, Parkinson C, Foley K et al (2019) Assessing radiomic feature robustness to interpolation in (18) F‑FDG PET imaging. Sci Rep 9(1):9649
Zwanenburg A, Vallières M, Abdalah MA et al (2020) The image biomarker standardization initiative: standardized quantitative radiomics for high-throughput image-based phenotyping. Radiology 295(2):328–338. https://doi.org/10.1148/radiol.2020191145
Zwanenburg A, Leger S, Vallières M et al (2016) Initiative, for the I. B. S. Image biomarker standardisation initiative (arXiv)
Tixier F, Hatt M, Le Rest CC et al (2012) Reproducibility of tumor uptake heterogeneity characterization through textural feature analysis in 18F-FDG PET. J Nucl Med 53:693–700
Vallieres M, Zwanenburg A, Badic B et al (2018) Responsible radiomics research for faster clinical translation. J Nucl Med 59(2):189–193
Belli ML, Mori M, Broggi S et al (2018) Quantifying the robustness of [18F]FDG-PET/CT radiomic features with respect to tumor delineation in head and neck and pancreatic cancer patients. Phys Med 49:105–111
Mori M, Benedetti G, Partelli S et al (2019) Ct radiomic features of pancreatic neuroendocrine neoplasms (panNEN) are robust against delineation uncertainty. Phys Med 57:41–46
Avanzo M, Gagliardi V, Stancanello J et al (2021) Combining computed tomography and biologically effective dose in radiomics and deep learning improves prediction of tumor response to robotic lung stereotactic body radiation therapy. Med Phys 48:6257–6269
Seuntjens J, Lartigau EF, Cora S et al (2014) ICRU report no. 91: prescribing, recording, and reporting of stereotactic treatments with small photon beams. J ICRU 14(2):1–152
Rogers W, Seetha ST, Refaee TAG et al (2020) Radiomics : from qualitative to quantitative imaging. Br J Radiol 93(1108):20190948. https://doi.org/10.1259/bjr.20190948
Lambin P, Leijenaar RTH, Deist TM et al (2017) Radiomics: the bridge between medical imaging and personalized medicine. Nat Rev Clin Oncol 14:749–762. https://doi.org/10.1038/nrclinonc.2017.141
Aerts HJWL, Velazquez ER, Leijenaar RTH et al (2014) Decoding tumour phenotype by noninvasive imaging using a quantitative radiomics approach. Nat Commun 5:4006. https://doi.org/10.1038/ncomms5006
Dercle L, Fronheiser M, Lu L et al (2020) Identifcation of non-small cell lung cancer sensitive to systemic cancer therapies using radiomics. Clin Cancer Res. https://doi.org/10.1158/1078-0432.CCR-19-2942
Mori M, Passoni P, Incerti E et al (2020) Training and validation of a robust PET radiomic-based index to predict distant-relapse-free-survival after radio-chemotherapy for locally advanced pancreatic cancer. Radiother Oncol 153:258–264. https://doi.org/10.1016/j.radonc.2020.07.003
Tang C, Hobbs B, Amer A et al (2018) Development of an immune-pathology informed radiomics model for non-small cell lung cancer. Sci Rep 8(1):1922. https://doi.org/10.1038/s41598-018-20471-5
Lee K, Le T, Hau E et al (2021) A systematic review into the radiological features predicting local recurrence after stereotactic ablative body radiotherapy (SABR) in patients with non-small cell lung cancer (NSCLC). Int J Radiat Oncol Biol Phys. https://doi.org/10.1016/j.ijrobp.2021.11.027
Osti MF, Agolli L, Valeriani M et al (2018) 30 Gy single dose stereotactic body radiation therapy (SBRT): report on outcome in a large series of patients with lung oligometastatic disease. Cancer Treat Res 122:165–170. https://doi.org/10.1016/j.lungcan.06.018
Helou J, Thibault I, Poon I et al (2017) Stereotactic ablative radiation therapy for pulmonary metastases: histology, dose, and indication matter. Int J Radiat Oncol Biol Phys 98(2):419–427. https://doi.org/10.1016/j.ijrobp.2017.02.093
Virbel G, Le Fèvre C, Noël G, Antoni D (2021) Stereotactic body radiotherapy for patients with lung oligometastatic disease: a five-year review. Cancers. https://doi.org/10.3390/cancers13143623
Badic B, Hatt M, Durand S et al (2019) Radiogenomics-based cancer prognosis in colorectal cancer. Sci Rep 9:9743
Moreira JM, Santiago I, Santinha J et al (2019) Challenges and promises of radiomics for rectal cancer. Curr Colorectal Cancer Rep 15:175–180
Formacon-Wood I, Faiver-Finn C, O’Connor JP, Price GJ (2020) Radiomics as a personalized medicine tool in lung cancer: separating the hope from the hype. Cancer Treat Res 146:197–208
Chang E, Joel MZ, Chang HY et al (2021) Comparison of radiomic feature aggregation methods for patients with multiple tumors. Sci Rep 11:9758
Acknowledgements
The authors thank Prof. Chiara Brombin (MSc, PhD, University Center for Statistics in the Biomedical Sciences, Vita-Salute San Raffaele University, Milan, Italy) for her help in drafting the final version of the statistical analysis.
Funding
Dr. Martina Mori, PhD, receives funds from the Italian Association for Cancer Research (AIRC, IG23150).
Author information
Authors and Affiliations
Corresponding author
Ethics declarations
Conflict of interest
A. Fodor, M. Mori, R. Tummineri, S. Broggi, C.L. Deantoni, P. Mangili, S. Baroni, S.L. Villa, I. Dell’Oca, A. Del Vecchio, C. Fiorino and N. Di Muzio declare that they have no competing interests.
Additional information
Data availability statement
The data that support the findings of this study (anonymized individual participant data) are available on request from the corresponding author to researchers who provide a methodologically sound proposal. Requests made to the corresponding author (AF) will be evaluated by the IRCCS San Raffaele Scientific Institute Ethics Committee.
Supplementary Information
66_2022_2034_MOESM1_ESM.tif
Fig. 1 Suppl.: The heat map of radiomic features extracted. The most correlated couplespairs of features according to the Spearman coefficient are reported in red and green
66_2022_2034_MOESM2_ESM.docx
CT radiomic predictors of local relapse after SBRT for lung oligometastases from colorectal cancer: a single Institute pilot study
Rights and permissions
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Fodor, A., Mori, M., Tummineri, R. et al. CT radiomic predictors of local relapse after SBRT for lung oligometastases from colorectal cancer: a single institute pilot study. Strahlenther Onkol 199, 477–484 (2023). https://doi.org/10.1007/s00066-022-02034-w
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00066-022-02034-w