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Value of tumor stiffness measured with MR elastography for assessment of response of hepatocellular carcinoma to locoregional therapy

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Abstract

Purpose

The aim of the study was to correlate tumor stiffness (TS) measured with MR elastography (MRE) with degree of tumor enhancement and necrosis on contrast-enhanced T1-weighted imaging (CE-T1WI) in hepatocellular carcinomas (HCC) treated with Yttrium-90 radioembolization (RE) or transarterial chemoembolization plus radiofrequency ablation (TACE/RFA).

Material and methods

This retrospective study was IRB-approved and the requirement for informed consent was waived. 52 patients (M/F 38/14, mean age 67 years) with HCC who underwent RE (n = 22) or TACE/RFA (n = 30) and 11 controls (M/F 6/5, mean age 64 years) with newly diagnosed untreated HCC were included. The MRI protocol included a 2D MRE sequence. TS and LS (liver stiffness) were measured on stiffness maps. Degree of tumor necrosis was assessed on subtraction images by two observers, and tumor enhancement ratios (ER) were calculated on CE-T1WI by one observer.

Results

63 HCCs (mean size 3.2 ± 1.6 cm) were evaluated. TS was significantly lower in treated vs. untreated tumors (3.9 ± 1.8 vs. 6.9 ± 3.4 kPa, p = 0.006) and also compared to LS (5.3 ± 2.2 kPa, p = 0.002). There were significant correlations between TS and each of enhancement ratios (r = 0.514, p = 0.0001), and percentage of necrosis (r = −0.540, p = 0.0001). The observed correlations were stronger in patients treated with RE (TS vs. ER, r = 0.636, TS vs. necrosis, r = −0.711, both p = 0.0001). Percentage of necrosis and T1-signal in native T1WI were significant independent predictors of TS (p = 0.0001 and 0.001, respectively).

Conclusion

TS measured with MRE shows a significant correlation with tumor enhancement and necrosis, especially in HCCs treated with RE.

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References

  1. El-Serag HB (2007) Epidemiology of hepatocellular carcinoma in USA. Hepatol Res 37(Suppl 2):S88–S94. doi:10.1111/j.1872-034X.2007.00168.x

    Article  PubMed  Google Scholar 

  2. Shields A, Reddy KR (2005) Hepatocellular carcinoma: current treatment strategies. Curr Treat Options Gastroenterol 8(6):457–466

    Article  PubMed  Google Scholar 

  3. Kulik LM, Atassi B, van Holsbeeck L, et al. (2006) Yttrium-90 microspheres (TheraSphere) treatment of unresectable hepatocellular carcinoma: downstaging to resection, RFA and bridge to transplantation. J Surg Oncol 94(7):572–586. doi:10.1002/jso.20609

    Article  CAS  PubMed  Google Scholar 

  4. Lu DS, Yu NC, Raman SS, et al. (2005) Radiofrequency ablation of hepatocellular carcinoma: treatment success as defined by histologic examination of the explanted liver. Radiology 234(3):954–960. doi:10.1148/radiol.2343040153

    Article  PubMed  Google Scholar 

  5. Maddala YK, Stadheim L, Andrews JC, et al. (2004) Drop-out rates of patients with hepatocellular cancer listed for liver transplantation: outcome with chemoembolization. Liver Transpl 10(3):449–455. doi:10.1002/lt.20099

    Article  PubMed  Google Scholar 

  6. Bruix J, Sherman M, Practice Guidelines Committee AAftSoLD (2005) Management of hepatocellular carcinoma. Hepatology 42(5):1208–1236. doi:10.1002/hep.20933

    Article  PubMed  Google Scholar 

  7. Llovet JM, Real MI, Montana X, et al. (2002) Arterial embolisation or chemoembolisation versus symptomatic treatment in patients with unresectable hepatocellular carcinoma: a randomised controlled trial. Lancet 359(9319):1734–1739. doi:10.1016/S0140-6736(02)08649-X

    Article  PubMed  Google Scholar 

  8. Morimoto M, Numata K, Kondou M, et al. (2010) Midterm outcomes in patients with intermediate-sized hepatocellular carcinoma: a randomized controlled trial for determining the efficacy of radiofrequency ablation combined with transcatheter arterial chemoembolization. Cancer 116(23):5452–5460. doi:10.1002/cncr.25314

    Article  PubMed  Google Scholar 

  9. Kim JH, Won HJ, Shin YM, et al. (2011) Medium-sized (3.1–5.0 cm) hepatocellular carcinoma: transarterial chemoembolization plus radiofrequency ablation versus radiofrequency ablation alone. Ann Surg Oncol 18(6):1624–1629. doi:10.1245/s10434-011-1673-8

    Article  PubMed  Google Scholar 

  10. Kim JW, Kim JH, Won HJ, et al. (2012) Hepatocellular carcinomas 2–3 cm in diameter: transarterial chemoembolization plus radiofrequency ablation vs. radiofrequency ablation alone. Eur J Radiol 81(3):e189–e193. doi:10.1016/j.ejrad.2011.01.122

    Article  PubMed  Google Scholar 

  11. Kim S, Mannelli L, Hajdu CH, et al. (2010) Hepatocellular carcinoma: assessment of response to transarterial chemoembolization with image subtraction. J Magn Reson Imaging 31(2):348–355. doi:10.1002/jmri.22038

    Article  PubMed  Google Scholar 

  12. Ehman RL, Crues JV, Lenkinski RE, et al. (1996) Magnetic resonance. Radiology 198(3):920–926. doi:10.1148/radiology.198.3.8628896

    Article  CAS  PubMed  Google Scholar 

  13. Muthupillai R, Ehman RL (1996) Magnetic resonance elastography. Nat Med 2(5):601–603

    Article  CAS  PubMed  Google Scholar 

  14. Muthupillai R, Lomas DJ, Rossman PJ, et al. (1995) Magnetic resonance elastography by direct visualization of propagating acoustic strain waves. Science 269(5232):1854–1857

    Article  CAS  PubMed  Google Scholar 

  15. Yin M, Talwalkar JA, Glaser KJ, et al. (2007) Assessment of hepatic fibrosis with magnetic resonance elastography. Clin Gastroenterol Hepatol 5(10):1207–1213. doi:10.1016/j.cgh.2007.06.012

    Article  PubMed  PubMed Central  Google Scholar 

  16. Garteiser P, Doblas S, Daire JL, et al. (2012) MR elastography of liver tumours: value of viscoelastic properties for tumour characterisation. Eur Radiol 22(10):2169–2177. doi:10.1007/s00330-012-2474-6

    Article  PubMed  Google Scholar 

  17. Venkatesh SK, Yin M, Glockner JF, et al. (2008) MR elastography of liver tumors: preliminary results. AJR Am J Roentgenol 190(6):1534–1540. doi:10.2214/AJR.07.3123

    Article  PubMed  PubMed Central  Google Scholar 

  18. Li J, Jamin Y, Boult JK, et al. (2014) Tumour biomechanical response to the vascular disrupting agent ZD6126 in vivo assessed by magnetic resonance elastography. Br J Cancer 110(7):1727–1732. doi:10.1038/bjc.2014.76

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  19. Pepin KM, Chen J, Glaser KJ, et al. (2014) MR elastography derived shear stiffness—a new imaging biomarker for the assessment of early tumor response to chemotherapy. Magn Reson Med 71(5):1834–1840. doi:10.1002/mrm.24825

    Article  PubMed  Google Scholar 

  20. Wald C, Russo MW, Heimbach JK, et al. (2013) New OPTN/UNOS policy for liver transplant allocation: standardization of liver imaging, diagnosis, classification, and reporting of hepatocellular carcinoma. Radiology 266(2):376–382. doi:10.1148/radiol.12121698

    Article  PubMed  Google Scholar 

  21. Motosugi U, Ichikawa T, Sou H, et al. (2012) Effects of gadoxetic acid on liver elasticity measurement by using magnetic resonance elastography. Magn Reson Imaging 30(1):128–132. doi:10.1016/j.mri.2011.08.005

    Article  CAS  PubMed  Google Scholar 

  22. Yasar TK, Wagner M, Bane O, et al. (2016) Interplatform reproducibility of liver and spleen stiffness measured with MR elastography. J Magn Reson Imaging 43(5):1064–1072. doi:10.1002/jmri.25077

    Article  PubMed  Google Scholar 

  23. Serai SD, Yin M, Wang H, Ehman RL, Podberesky DJ (2015) Cross-vendor validation of liver magnetic resonance elastography. Abdom Imaging 40(4):789–794. doi:10.1007/s00261-014-0282-y

    Article  PubMed  PubMed Central  Google Scholar 

  24. Silva AM, Grimm RC, Glaser KJ, et al. (2015) Magnetic resonance elastography: evaluation of new inversion algorithm and quantitative analysis method. Abdom Imaging 40(4):810–817. doi:10.1007/s00261-015-0372-5

    Article  PubMed  Google Scholar 

  25. Hennedige TP, Hallinan JT, Leung FP, et al. (2016) Comparison of magnetic resonance elastography and diffusion-weighted imaging for differentiating benign and malignant liver lesions. Eur Radiol 26(2):398–406. doi:10.1007/s00330-015-3835-8

    Article  PubMed  Google Scholar 

  26. Asbach P, Klatt D, Schlosser B, et al. (2010) Viscoelasticity-based staging of hepatic fibrosis with multifrequency MR elastography. Radiology 257(1):80–86. doi:10.1148/radiol.10092489

    Article  PubMed  Google Scholar 

  27. Kierans AS, Elazzazi M, Braga L, et al. (2010) Thermoablative treatments for malignant liver lesions: 10-year experience of MRI appearances of treatment response. AJR Am J Roentgenol 194(2):523–529. doi:10.2214/AJR.09.2621

    Article  PubMed  Google Scholar 

  28. Riaz A, Kulik L, Lewandowski RJ, et al. (2009) Radiologic-pathologic correlation of hepatocellular carcinoma treated with internal radiation using yttrium-90 microspheres. Hepatology 49(4):1185–1193. doi:10.1002/hep.22747

    Article  PubMed  Google Scholar 

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Correspondence to Bachir Taouli.

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Funding

This study was funded by National Institutes of Health (NIH R01 Grant EB001981), Schweizerischer Nationalfonds zur Förderung der Wissenschaftlichen Forschung (Fellowship P2ZHP3_161691).

Conflict of interest

The authors declare that they have no conflict of interest.

Ethical approval

All procedures performed in studies involving human participants were in accordance with the ethical standards of the institutional and/or national research committee and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. For this type of study formal consent is not required.

Informed consent

Statement of informed consent was not applicable since the manuscript does not contain any patient data.

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Gordic, S., Ayache, J.B., Kennedy, P. et al. Value of tumor stiffness measured with MR elastography for assessment of response of hepatocellular carcinoma to locoregional therapy. Abdom Radiol 42, 1685–1694 (2017). https://doi.org/10.1007/s00261-017-1066-y

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  • DOI: https://doi.org/10.1007/s00261-017-1066-y

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