Study of diagnostic efficacy in detecting liver metastases using T1-weighted contrast-enhanced studies with magnetization transfer contrast effect
https://doi.org/10.24835/1607-0763-1472
Abstract
Objective: To evaluate the diagnostic capabilities of detecting metastatic lesions on post-contrast images using magnetization transfer contrast with a short fat-suppressed presaturation pulse.
Materials and methods. The study material consisted of dynamic contrast-enhanced MR images of abdominal organs with metastatic liver involvement. Parameters of the pre-saturation pulse: Δf = -210 Hz, FA = 600°. Contrast ratio (CR) was calculated for each focus using a formula: CR = ((IFOCUS – ILIVER) / ILIVER) • 100%. Vascularization was assessed on a scale of 3 categories: hypovascular, isovascular, and hypervascular. Threshold values for each category were calculated using cluster analysis. To assess the sensitivity of focus detection, they were divided into groups by size: Group 1 − from 5 mm to 10 mm; Group 2 − from 10 mm to 20 mm. Statistical analysis of the results was performed using the Mann-Whitney, Wilcoxon, Cochran, and McNemar criteria.
Results. In the course of the clinical study, heterogeneous groups of patients were obtained in terms of gender and age depending on the nature of vascularization of liver foci during analysis of the arterial phase of DCE: hypervascular (n = 14) and hypovascular (n = 38), with a total of 52 studies conducted, as one patient had dynamic control. The threshold value for the group of hypervascular metastases was identified as CR > 49.6%. In Group 1 (5 mm to 10 mm), the sensitivity of detecting foci on post-contrast images T-TSE-MTC was 47.7%. In Group 2, there were no statistically significant differences between the diagnosis of foci sized 10 mm or larger on post-contrast images T1-TSE-MTC and all phases of DCE (p < 0.0001), with a sensitivity of 100%.
Conclusions. 1. According to cluster analysis, T1-weighted study based on fast spin echo with magnetization transfer contrast (T1-TSE-MTC) allows differentiation of hypervascular metastases from transitional and hypovascular (p < 0.05).
- The contrast of hypervascular metastases in the post-contrast phase on T1-TSE-MTC images does not significantly differ from the arterial phase of dynamic contrast enhancement (DCE) (p > 0.05).
- A high sensitivity to enhancement by paramagnetics at low concentrations on T1-TSE-MTC images was revealed, which reduces the contrast of hypovascular metastatic foci sized 5 to 10 mm with a significant decrease in their detection compared to DCE (p < 0.05), while for sizes 10 to 20 mm, no significant differences with DCE were found (p > 0.05).
About the Authors
M. Yu. SannikovRussian Federation
Maxim Yu. Sannikov – radiologist of the X-ray diagnostics department, Tomsk Regional Oncology Dispensary, Tomsk.
E-mail: sannikoff.maks@yandex.ru
O. Yu. Borodin
Tomsk Regional Oncology Dispensary; Siberian State Medical University
Russian Federation
Oleg Yu. Borodin – Doct. of Sci. (Med.), Head of the X-ray diagnostics department, Tomsk Regional Oncology Dispensary;
Professor of the Department of Biophysics and Functional Diagnostics, Siberian State Medical University, Tomsk.
https://orcid.org/0000-0002-5031-1355
References
1. Lomovtseva K. Kh., Karmazanovsky G. G. Diffusion-weighted images in focal liver pathology: a literature review. Medical Visualization. 2015; 6: 50–60. (In Russian)
2. Akchurina E.D. Diffusion-weighted images in complex radiological diagnostics of focal liver lesions. Autoref. ... Dis. Cand. of Sci. (Med.). Moscow, 2011. 24 p. (In Russian)
3. Asato N., Tsurusaki M., Sofue K. et al. Comparison of gadoxetic acid-enhanced dynamic MR imaging and contrast-enhanced computed tomography for preoperative evaluation of colorectal liver metastases. Jpn. J. Radiol. 2017; 35 (4): 197–205. http://doi.org/10.1007/s11604-017-0622-2
4. Chen S.Z., Yuan J., Deng M. et al. Chemical exchange saturation transfer (CEST) MR technique for in-vivo liver imaging at 3.0 tesla. Eur. Radiol. 2016; 26 (6): 1792–800. http://doi.org/10.1007/s00330-015-3972-0
5. Lupescu I.G., Nicolae C.A., Pomohaci M. et al. Multiparametric MRI with gadoxetic acid (Primovist®) in oncological patients: current indications and utility of the hepatobiliary phase. Oncolog-Hematolog.ro. Oncolog-Hematolog. 2023. 64 (3): 11–14.
6. Choi S.H., Kim S.Y., Park S.H. et al. Diagnostic performance of CT, gadoxetate disodium-enhanced MRI, and PET/CT for the diagnosis of colorectal liver metastasis: Systematic review and meta-analysis. J. Magn. Reson. Imaging. 2018; 47 (5): 1237–1250. http://doi.org/10.1002/jmri.25852
7. van der Reijd D.J., Chupetlovska K., van Dijk E. et al. Multi-sequence MRI radiomics of colorectal liver metastases: Which features are reproducible across readers? Eur. J. Radiol. 2024; 172: 111346. http://doi.org/10.1016/j.ejrad.2024.111346
8. Liver cancer (hepatocellular). Clinical guidelines. Approved by the Scientific Council of the Ministry of Health of the Russian Federation. Moscow, 2020. 57 p. https://oncology-association.ru/wp-content/uploads/2020/09/rak_pecheni.pdf?ysclid=m27xr4av1i458055995
9. Braga L., Semelka R.C., Pietrobon R. et al. Does hypervascularity of liver metastases as detected on MRI predict disease progression in breast cancer patients? Am. J. Roentgenol. 2004; 182 (5): 1207–1213. http://doi.org/10.2214/ajr.182.5.1821207
10. Semelka R.C., Helmberger T.K. Contrast agents for MR imaging of the liver. Radiology. 2001; 218 (1): 27–38. http://doi.org/10.1148/radiology.218.1.r01ja2427
11. Berry I., Barker G.J., Barkhof F. et al. A multicenter measurement of magnetization transfer ratio in normal white matter. J. Magn. Reson. Imaging. 1999; 9 (3): 441–446. http://doi.org/10.1002/(sici)1522-2586(199903)9:3<441::aid-jmri12>3.0.co;2-r
12. Чижиков В.И. Практикум по магнитному резонансу. СПб.: Изд-во С.-Петербургского университета, 2009. 254 с.
13. Chizhikov V.I. Practical guide to magnetic resonance imaging. St. Petersburg: Publishing house of St. Petersburg University, 2009. 254 p. (In Russian)
14. Ebrahimi B., Jiang K., Lerman L. Magnetization Transfer Imaging. In: Serai S.D., Darge K. (eds). Advanced Clinical MRI of the Kidney. Springer, Cham., 2023: 181–195. http://doi.org/10.1007/978-3-031-40169-5_13
15. Wáng Y.X.J., Dou W., Shen Z., Zhang Y. An update on liver chemical exchange saturation transfer imaging with a focus on clinical translation. Quant. Imaging Med. Surg. 2023; 13 (7): 4057–4076. http://doi.org/10.21037/qims-23-379
16. Mahfouz M., Zaky I., Maher M. Magnetization Transfer Magnetic Resonance Imaging of Hepatic Tumors. J. Egypt. Nat. Cancer Inst. 2000; 12 (3) 191–198.
17. Rosenkrantz A.B., Storey P., Gilet A.G. et al. Magnetization transfer contrast-prepared MR imaging of the liver: inability to distinguish healthy from cirrhotic liver. Radiology. 2012; 262 (1): 136–143. http://doi.org/10.1148/radiol.11111043
18. Seo N., Jeong H.K., Choi J.Y. et al. Liver MRI with amide proton transfer imaging: feasibility and accuracy for the characterization of focal liver lesions. Eur. Radiol. 2021; 31 (1): 222–231. http://doi.org/10.1007/s00330-020-07122-y
19. Choi J.Y., Choi J.S., Kim M.J. et al. Detection of hepatic hypovascular metastases: 3D gradient echo MRI using a hepatobiliary contrast agent. J. Magn. Reson. Imaging. 2010 Mar; 31 (3): 571–578. http://doi.org/10.1002/jmri.22076
20. Maino C., Vernuccio F., Cannella R. et al. Liver metastases: The role of magnetic resonance imaging. Wld J. Gastroenterol. 2023; 29 (36): 5180–5197. http://doi.org/10.3748/wjg.v29.i36.5180
21. Vernuccio F., Cannella R., Bartolotta T.V. et al. Advances in liver US, CT, and MRI: moving toward the future. Eur. Radiol. Exp. 2021; 5 (1): 52. http://doi.org/10.1186/s41747-021-00250-0
22. Zhang L., Yu X., Huo L. et al. Detection of liver metastases on gadobenate dimeglumine-enhanced MRI: systematic review, meta-analysis, and similarities with gadoxetate-enhanced MRI. Eur. Radiol. 2019; 29 (10): 5205–5216. http://doi.org/10.1007/s00330-019-06110-1
23. Mao Y., Chen B., Wang H. et al. Diagnostic performance of magnetic resonance imaging for colorectal liver metastasis: A systematic review and meta-analysis. Sci. Rep. 2020; 10 (1): 1969. http://doi.org/10.1038/s41598-020-58855-1
24. Morin C., Drolet S., Daigle C. et al. Additional value of gadoxetic acid-enhanced MRI to conventional extracellular gadolinium-enhanced MRI for the surgical management of colorectal and neuroendocrine liver metastases. HPB (Oxford). 2020; 22 (5): 710–715. http://doi.org/10.1016/j.hpb.2019.09.009
25. Hayoz R., Vietti-Violi N., Duran R. et al. The combination of hepatobiliary phase with Gd-EOB-DTPA and DWI is highly accurate for the detection and characterization of liver metastases from neuroendocrine tumor. Eur. Radiol. 2020; 30 (12): 6593–6602. http://doi.org/10.1007/s00330-020-06930-6
26. Schnitzer M.L., Buchner J., Biechele G. et al. Economic evaluation of 18F-FDG PET/CT, MRI and CE-CT in selection of colorectal liver metastases eligible for ablation - A cost-effectiveness analysis. Eur. J. Radiol. 2023; 163: 110803. http://doi.org/10.1016/j.ejrad.2023.110803
Review
For citations:
Sannikov M.Yu., Borodin O.Yu. Study of diagnostic efficacy in detecting liver metastases using T1-weighted contrast-enhanced studies with magnetization transfer contrast effect. Medical Visualization. 2025;29(1):62-70. (In Russ.) https://doi.org/10.24835/1607-0763-1472