Quantitative MRI for Assessment of Treatment Outcomes in a Rabbit VX2 Hepatic Tumor Model.


Journal

Journal of magnetic resonance imaging : JMRI
ISSN: 1522-2586
Titre abrégé: J Magn Reson Imaging
Pays: United States
ID NLM: 9105850

Informations de publication

Date de publication:
09 2020
Historique:
received: 23 07 2019
revised: 24 09 2019
accepted: 25 09 2019
pubmed: 13 11 2019
medline: 15 5 2021
entrez: 13 11 2019
Statut: ppublish

Résumé

Globally, primary and secondary liver cancer is one of the most common cancer types, accounting 8.2% of deaths worldwide in 2018. One of the key strategies to improve the patient's prognosis is the early diagnosis, when liver function is still preserved. In hepatocellular carcinoma (HCC), the typical wash-in/wash-out pattern in conventional magnetic resonance imaging (MRI) reaches a sensitivity of 60% and specificity of 96-100%. However, in recent years functional MRI sequences such as hepatocellular-specific gadolinium-based dynamic-contrast enhanced MRI, diffusion-weighted imaging (DWI), and magnetic resonance spectroscopy (MRS) have been demonstrated to improve the evaluation of treatment success and thus the therapeutic decision-making and the patient's outcome. In the preclinical research setting, the VX2 liver rabbit tumor, which once originated from a virus-induced anaplastic squamous cell carcinoma, has played a longstanding role in experimental interventional oncology. Especially the high tumor vascularity allows assessing the treatment response of locoregional interventions such as radiofrequency ablation (RFA) and transcatheter arterial embolization (TACE). Functional MRI has been used to monitor the tumor growth and viability following interventional treatment. Besides promising results, a comprehensive overview of functional MRI sequences used so far in different treatment setting is lacking, thus lowering the comparability of study results. This review offers a comprehensive overview of study protocols, results, and limitations of quantitative MRI sequences applied to evaluate the treatment outcome of VX2 hepatic tumor models, thus generating a unique basis for future MRI studies and potential translation into the clinical setting. Level of Evidence: 2 Technical Efficacy: Stage 1 J. MAGN. RESON. IMAGING 2019. J. Magn. Reson. Imaging 2020;52:668-685.

Identifiants

pubmed: 31713973
doi: 10.1002/jmri.26968
doi:

Substances chimiques

Contrast Media 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't Review

Langues

eng

Sous-ensembles de citation

IM

Pagination

668-685

Informations de copyright

© 2019 International Society for Magnetic Resonance in Medicine.

Références

Siegel RL, Miller KD, Jemal A. Cancer statistics, 2019. CA Cancer J Clin 2019;69:7-34.
Bray F, Ferlay J, Soerjomataram I, Siegel RL, Torre LA, Jemal A. Global cancer statistics 2018: GLOBOCAN estimates of incidence and mortality worldwide for 36 cancers in 185 countries. CA Cancer J Clin 2018;68:394-424.
White SB, Chen J, Gordon AC, et al. Percutaneous ultrasound guided implantation of VX2 for creation of a rabbit hepatic tumor model. PLoS One 2015;10:e0123888.
Rous P, Beard JW. The progression to carcinoma of virus-induced rabbit papillomas (Shope). J Exp Med 1935;62:523-548.
Kidd JG, Rous P. A transplantable rabbit carcinoma originating in a virus-induced papilloma and containing the virus in masked or altered form. J Exp Med 1940;71:813-838.
Galasko CS, Muckle DS. Intrasarcolemmal proliferation of the VX2 carcinoma. Br J Cancer 1974;29:59-65.
Burgener FA. Peripheral hepatic artery embolization in rabbits with VX2 carcinomas of the liver. Cancer 1980;46:56-63.
Hoye RC, Thomas LB, Riggle GC, Ketcham A. Effects of neodymium laser on normal liver and Vx2 carcinoma transplanted into the liver of experimental animals. J Natl Cancer Inst 1968;41:1071-1082.
Lee JM, Kim SW, Chung GH, Lee SY, Han YM, Kim CS. Open radio-frequency thermal ablation of renal VX2 tumors in a rabbit model using a cooled-tip electrode: Feasibility, safety, and effectiveness. Eur Radiol 2003;13:1324-1332.
Frank JA, Girton M, Dwyer AJ, et al. A reproducible model of metastatic brain and ocular tumor by hematogenous inoculation of the VX2 tumor in rabbits. J Neurosurg 1987;67:106-109.
Anayama T, Nakajima T, Dunne M, et al. A novel minimally invasive technique to create a rabbit VX2 lung tumor model for nano-sized image contrast and interventional studies. PLoS One 2013;8:e67355.
Rhee TK, Ryu RK, Bangash AK, et al. Rabbit VX2 tumors as an animal model of uterine fibroids and for uterine artery embolization. J Vasc Interv Radiol 2007;18:411-418.
Handal JA, Schulz JF, Florez GB, Kwok SC, Khurana JS, Samuel SP. Creation of rabbit bone and soft tissue tumor using cultured VX2 cells. J Surg Res 2013;179:e127-132.
Chen J, Qian T, Zhang H, Wei C, Meng F, Yin H. Combining dynamic contrast enhanced magnetic resonance imaging and microvessel density to assess the angiogenesis after PEI in a rabbit VX2 liver tumor model. Magn Reson Imaging 2016;34:177-182.
Guo WC, He XF, Li YH, Li ZH, Mei QL, Chen Y. The effect of sequential transcatheter arterial chemoembolization (TACE) and portal venous embolizations (PVE) vs. TACE or PVE alone on rabbit VX2 liver carcinoma and on liver regeneration. Eur Rev Med Pharmacol Sci 2016;20:3186-3193.
Gaba RC, Emmadi R, Parvinian A, Casadaban LC. Correlation of doxorubicin delivery and tumor necrosis after drug-eluting bead transarterial chemoembolization of rabbit VX2 liver tumors. Radiology 2016;280:752-761.
Tacher V, Duran R, Lin M, et al. Multimodality imaging of ethiodized oil-loaded radiopaque microspheres during transarterial embolization of rabbits with VX2 liver tumors. Radiology 2016;279:741-753.
Gao F, Qian T, Chen MZ, Yin HB, Xu YL. Therapeutic effects of transarterial infusion of lipiodol and ethanol in various ratios in a rabbit VX2 tumor model. Diagn Interv Radiol 2015;21:241-246.
Shanshan L, Feng S, Kaikai W, Yijun Z, Huiming L, Chuanmiao X. Intravoxel incoherent motion diffusion-weighted MR imaging for early evaluation of the effect of radiofrequency ablation in rabbit liver VX2 tumors. Acad Radiol 2018;25:1128-1135.
Prat F, Centarti M, Sibille A, et al. Extracorporeal high-intensity focused ultrasound for VX2 liver tumors in the rabbit. Hepatology 1995;21:832-836.
Virmani S, Harris KR, Szolc-Kowalska B, et al. Comparison of two different methods for inoculating VX2 tumors in rabbit livers and hind limbs. J Vasc Interv Radiol 2008;19:931-936.
Parvinian A, Casadaban LC, Gaba RC. Development, growth, propagation, and angiographic utilization of the rabbit VX2 model of liver cancer: A pictorial primer and "how to" guide. Diagn Interv Radiol 2014;20:335-340.
Sun JH, Zhang YL, Nie CH, et al. Considerations for two inoculation methods of rabbit hepatic tumors: Pathology and image features. Exp Ther Med 2012;3:386-390.
Chen JH, Lin YC, Huang YS, Chen TJ, Lin WY, Han KW. Induction of VX2 carcinoma in rabbit liver: Comparison of two inoculation methods. Lab Anim 2004;38:79-84.
Luo W, Zhou X, Zheng X, et al. Role of sonography for implantation and sequential evaluation of a VX2 rabbit liver tumor model. J Ultrasound Med 2010;29:51-60.
Wang D, Bangash AK, Rhee TK, et al. Liver tumors: Monitoring embolization in rabbits with VX2 tumors-Transcatheter intraarterial first-pass perfusion MR imaging. Radiology 2007;245:130-139.
Moon J, Kim JH, Choi D, et al. Correlation of quantitative dynamic contrast-enhanced MRI with microvascular density in necrotic, partial necrotic, and viable liver tumors in a rabbit model. J Appl Clin Med Phys 2016;17:418-427.
Liu Y, Lu L, Jin H, et al. Radiofrequency ablation of liver VX2 tumor: Experimental results with MR diffusion-weighted imaging at 3.0T. PLoS One 2014;9:e104239.
Joo I, Lee JM, Grimm R, Han JK, Choi BI. Monitoring vascular disrupting therapy in a rabbit liver tumor model: Relationship between tumor perfusion parameters at IVIM diffusion-weighted MR imaging and those at dynamic contrast-enhanced MR imaging. Radiology 2016;278:104-113.
Shao H, Ni Y, Zhang J, et al. Dynamic contrast-enhanced and diffusion-weighted magnetic resonance imaging noninvasive evaluation of vascular disrupting treatment on rabbit liver tumors. PLoS One 2013;8:e82649.
Yang RM, Zou Y, Huang DP, et al. In vivo assessment of the vascular disrupting effect of M410 by DCE-MRI biomarker in a rabbit model of liver tumor. Oncol Rep 2014;32:709-715.
Buijs M, Vossen JA, Geschwind JF, et al. Quantitative proton MR spectroscopy as a biomarker of tumor necrosis in the rabbit VX2 liver tumor. J Vasc Interv Radiol 2011;22:1175-1180.
Deng J, Rhee TK, Sato KT, et al. In vivo diffusion-weighted imaging of liver tumor necrosis in the VX2 rabbit model at 1.5 Tesla. Invest Radiol 2006;41:410-414.
Vossen JA, Buijs M, Geschwind JF, et al. Diffusion-weighted and Gd-EOB-DTPA-contrast-enhanced magnetic resonance imaging for characterization of tumor necrosis in an animal model. J Comput Assist Tomogr 2009;33:626-630.
Li JL, Ye WT, Liu ZY, et al. Comparison of microvascular perfusion evaluation among IVIM-DWI, CT perfusion imaging and histological microvessel density in rabbit liver VX2 tumors. Magn Reson Imaging 2018;46:64-69.
Wu H, Hu M, Liu Z, et al. Intravoxel incoherent motion diffusion-weighted MRI for characterizing regional variability and monitoring serial changes of parameters in rabbit VX2 liver tumors. J Magn Reson Imaging 2016;43:173-180.
Wu H, Liu H, Liang C, et al. Diffusion-weighted multiparametric MRI for monitoring longitudinal changes of parameters in rabbit VX2 liver tumors. J Magn Reson Imaging 2016;44:707-714.
Chow AM, Gao DS, Fan SJ, et al. Liver fibrosis: An intravoxel incoherent motion (IVIM) study. J Magn Reson Imaging 2012;36:159-167.
Klauss M, Mayer P, Maier-Hein K, et al. IVIM-diffusion-MRI for the differentiation of solid benign and malign hypervascular liver lesions-Evaluation with two different MR scanners. Eur J Radiol 2016;85:1289-1294.
Zhang Y, Liu H, Xiao W, et al. Quantitative dynamic contrast-enhanced magnetic resonance imaging in a VX2 rabbit liver tumour model using different gadolinium-based contrast agents: Comparison of DCE-MRI quantitative results between Magnevist and Eovist. BJR Case Rep 2017;3:20160099.
Xiang Z, Liang Q, Liang C, Zhong G. The correlation of contrast-enhanced ultrasound and MRI perfusion quantitative analysis in rabbit VX2 liver cancer. Cell Biochem Biophys 2014;70:1859-1867.
Le Bihan D. Molecular diffusion, tissue microdynamics and microstructure. NMR Biomed 1995;8:375-386.
Le Bihan D, Breton E, Lallemand D, Grenier P, Cabanis E, Laval-Jeantet M. MR imaging of intravoxel incoherent motions: Application to diffusion and perfusion in neurologic disorders. Radiology 1986;161:401-407.
Li YT, Cercueil JP, Yuan J, Chen W, Loffroy R, Wang YX. Liver intravoxel incoherent motion (IVIM) magnetic resonance imaging: A comprehensive review of published data on normal values and applications for fibrosis and tumor evaluation. Quant Imaging Med Surg 2017;7:59-78.
Murphy P, Hooker J, Ang B, et al. Associations between histologic features of nonalcoholic fatty liver disease (NAFLD) and quantitative diffusion-weighted MRI measurements in adults. J Magn Reson Imaging 2015;41:1629-1638.
Grech-Sollars M, Hales PW, Miyazaki K, et al. Multi-centre reproducibility of diffusion MRI parameters for clinical sequences in the brain. NMR Biomed 2015;28:468-485.
Lee Y, Lee SS, Kim N, et al. Intravoxel incoherent motion diffusion-weighted MR imaging of the liver: Effect of triggering methods on regional variability and measurement repeatability of quantitative parameters. Radiology 2015;274:405-415.
Barbieri S, Donati OF, Froehlich JM, Thoeny HC. Comparison of intravoxel incoherent motion parameters across MR imagers and field strengths: Evaluation in upper abdominal organs. Radiology 2016;279:784-794.
Voert EE, Delso G, Porto M, Huellner M, Veit-Haibach P. Intravoxel Incoherent Motion Protocol Evaluation and Data Quality in Normal and Malignant Liver Tissue and Comparison to the Literature. Invest Radiol. 2016;51(2):90-99. https://doi.org/10.1097/RLI.0000000000000207. PMID: 26405835.
Youn BJ, Chung JW, Son KR, et al. Diffusion-weighted MR: Therapeutic evaluation after chemoembolization of VX-2 carcinoma implanted in rabbit liver. Acad Radiol 2008;15:593-600.
Qian T, Chen M, Gao F, Meng F, Gao X, Yin H. Diffusion-weighted magnetic resonance imaging to evaluate microvascular density after transarterial embolization ablation in a rabbit VX2 liver tumor model. Magn Reson Imaging 2014;32:1052-1057.
Le Bihan D. What can we see with IVIM MRI? Neuroimage 2019;187:56-67.
Park YS, Lee CH, Kim JH, et al. Using intravoxel incoherent motion (IVIM) MR imaging to predict lipiodol uptake in patients with hepatocellular carcinoma following transcatheter arterial chemoembolization: A preliminary result. Magn Reson Imaging 2014;32:638-646.
Wei Y, Huang Z, Tang H, et al. IVIM improves preoperative assessment of microvascular invasion in HCC. Eur Radiol 2019;29:5403-5414.
Ingrisch M, Sourbron S. Tracer-kinetic modeling of dynamic contrast-enhanced MRI and CT: A primer. J Pharmacokinet Pharmacodyn 2013;40:281-300.
Chen BB, Shih TT. DCE-MRI in hepatocellular carcinoma-clinical and therapeutic image biomarker. World J Gastroenterol 2014;20:3125-3134.
Koh TS, Bisdas S, Koh DM, Thng CH. Fundamentals of tracer kinetics for dynamic contrast-enhanced MRI. J Magn Reson Imaging 2011;34:1262-1276.
Van Beers BE, Pastor CM, Hussain HK. Primovist, Eovist: What to expect? J Hepatol 2012;57:421-429.
Hammerstingl R, Huppertz A, Breuer J, et al. Diagnostic efficacy of gadoxetic acid (Primovist)-enhanced MRI and spiral CT for a therapeutic strategy: Comparison with intraoperative and histopathologic findings in focal liver lesions. Eur Radiol 2008;18:457-467.
Ahn SS, Kim MJ, Lim JS, Hong HS, Chung YE, Choi JY. Added value of gadoxetic acid-enhanced hepatobiliary phase MR imaging in the diagnosis of hepatocellular carcinoma. Radiology 2010;255:459-466.
Di Martino M, Marin D, Guerrisi A, et al. Intraindividual comparison of gadoxetate disodium-enhanced MR imaging and 64-section multidetector CT in the detection of hepatocellular carcinoma in patients with cirrhosis. Radiology 2010;256:806-816.
Vogl TJ, Kummel S, Hammerstingl R, et al. Liver tumors: Comparison of MR imaging with Gd-EOB-DTPA and Gd-DTPA. Radiology 1996;200:59-67.
Sourbron S, Sommer WH, Reiser MF, Zech CJ. Combined quantification of liver perfusion and function with dynamic gadoxetic acid-enhanced MR imaging. Radiology 2012;263:874-883.
Juluru K, Talal AH, Yantiss RK, et al. Diagnostic accuracy of intracellular uptake rates calculated using dynamic Gd-EOB-DTPA-enhanced MRI for hepatic fibrosis stage. J Magn Reson Imaging 2017;45:1177-1185.
Buonaccorsi GA, O'Connor JP, Caunce A, et al. Tracer kinetic model-driven registration for dynamic contrast-enhanced MRI time-series data. Magn Reson Med 2007;58:1010-1019.
Hamy V, Dikaios N, Punwani S, et al. Respiratory motion correction in dynamic MRI using robust data decomposition registration - Application to DCE-MRI. Med Image Anal 2014;18:301-313.
Hsu CY, Shen YC, Yu CW, et al. Dynamic contrast-enhanced magnetic resonance imaging biomarkers predict survival and response in hepatocellular carcinoma patients treated with sorafenib and metronomic tegafur/uracil. J Hepatol 2011;55:858-865.
Jarnagin WR, Schwartz LH, Gultekin DH, et al. Regional chemotherapy for unresectable primary liver cancer: Results of a phase II clinical trial and assessment of DCE-MRI as a biomarker of survival. Ann Oncol 2009;20:1589-1595.
Liang PC, Ch'ang HJ, Hsu C, Tseng SS, Shih TT, Wu Liu T. Dynamic MRI signals in the second week of radiotherapy relate to treatment outcomes of hepatocellular carcinoma: A preliminary result. Liver Int 2007;27:516-528.
Wang B, Gao ZQ, Yan X. Correlative study of angiogenesis and dynamic contrast-enhanced magnetic resonance imaging features of hepatocellular carcinoma. Acta Radiol 2005;46:353-358.
Llovet JM, Real MI, Montana X, et al. Arterial embolisation or chemoembolisation versus symptomatic treatment in patients with unresectable hepatocellular carcinoma: A randomised controlled trial. Lancet 2002;359:1734-1739.
Lewandowski RJ, Wang D, Gehl J, et al. A comparison of chemoembolization endpoints using angiographic versus transcatheter intraarterial perfusion/MR imaging monitoring. J Vasc Interv Radiol 2007;18:1249-1257.
Virmani S, Wang D, Harris KR, et al. Comparison of transcatheter intraarterial perfusion MR imaging and fluorescent microsphere perfusion measurements during transcatheter arterial embolization of rabbit liver tumors. J Vasc Interv Radiol 2007;18:1280-1286.
Sato KT, Wang D, Lewandowski RJ, et al. Four-dimensional transcatheter intraarterial perfusion MRI monitoring of radiofrequency ablation of rabbit VX2 liver tumors. J Magn Reson Imaging 2011;34:563-569.
Gaba RC, Wang D, Lewandowski RJ, et al. Four-dimensional transcatheter intraarterial perfusion MR imaging for monitoring chemoembolization of hepatocellular carcinoma: Preliminary results. J Vasc Interv Radiol 2008;19:1589-1595.
Brown DB, Geschwind JF, Soulen MC, Millward SF, Sacks D. Society of Interventional Radiology position statement on chemoembolization of hepatic malignancies. J Vasc Interv Radiol 2006;17(2 Pt 1):217-223.
Wang D, Jin B, Lewandowski RJ, et al. Quantitative 4D transcatheter intraarterial perfusion MRI for monitoring chemoembolization of hepatocellular carcinoma. J Magn Reson Imaging 2010;31:1106-1116.
Wang D, Virmani S, Tang R, et al. Four-dimensional transcatheter intraarterial perfusion (TRIP)-MRI for monitoring liver tumor embolization in VX2 rabbits. Magn Reson Med 2008;60:970-975.
Wang D, Gaba RC, Jin B, et al. Intraprocedural transcatheter intra-arterial perfusion MRI as a predictor of tumor response to chemoembolization for hepatocellular carcinoma. Acad Radiol 2011;18:828-836.
Wang D, Gaba RC, Jin B, et al. Perfusion reduction at transcatheter intraarterial perfusion MR imaging: A promising intraprocedural biomarker to predict transplant-free survival during chemoembolization of hepatocellular carcinoma. Radiology 2014;272:587-597.
Kuo YT, Li CW, Chen CY, Jao J, Wu DK, Liu GC. In vivo proton magnetic resonance spectroscopy of large focal hepatic lesions and metabolite change of hepatocellular carcinoma before and after transcatheter arterial chemoembolization using 3.0-T MR scanner. J Magn Reson Imaging 2004;19:598-604.
Bawden SJ, Scott RA, Aithal GP. Current and future magnetic resonance technologies for assessing liver disease in clinical and experimental medicine. Dig Dis 2017;35:314-322.
Machann J, Stefan N, Schick F. (1)H MR spectroscopy of skeletal muscle, liver and bone marrow. Eur J Radiol 2008;67:275-284.
Tang ZY, Zhao JN, Zhong WJ, et al. The value of proton magnetic resonance spectroscopy in high-intensity focused ultrasound treatment of experimental liver cancer. Transl Oncol 2015;8:163-168.
Chen CY, Li CW, Kuo YT, et al. Early response of hepatocellular carcinoma to transcatheter arterial chemoembolization: Choline levels and MR diffusion constants-Initial experience. Radiology 2006;239:448-456.
Bian DJ, Xiao EH, Hu DX, et al. Magnetic resonance spectroscopy on hepatocellular carcinoma after transcatheter arterial chemoembolization. Chin J Cancer 2010;29:198-201.
Jagannathan NR, Kumar M, Seenu V, et al. Evaluation of total choline from in-vivo volume localized proton MR spectroscopy and its response to neoadjuvant chemotherapy in locally advanced breast cancer. Br J Cancer 2001;84:1016-1022.
Kumar M, Jagannathan NR, Seenu V, Dwivedi SN, Julka PK, Rath GK. Monitoring the therapeutic response of locally advanced breast cancer patients: Sequential in vivo proton MR spectroscopy study. J Magn Reson Imaging 2006;24:325-332.
Ogawa S, Menon RS, Tank DW, et al. Functional brain mapping by blood oxygenation level-dependent contrast magnetic resonance imaging. A comparison of signal characteristics with a biophysical model. Biophys J 1993;64:803-812.
Thomas CD, Chenu E, Walczak C, Plessis MJ, Perin F, Volk A. Morphological and carbogen-based functional MRI of a chemically induced liver tumor model in mice. Magn Reson Med 2003;50:522-530.
Howe FA, Robinson SP, McIntyre DJ, Stubbs M, Griffiths JR. Issues in flow and oxygenation dependent contrast (FLOOD) imaging of tumours. NMR Biomed 2001;14:497-506.
Baudelet C, Gallez B. How does blood oxygen level-dependent (BOLD) contrast correlate with oxygen partial pressure (pO2) inside tumors? Magn Reson Med 2002;48:980-986.
Jajamovich GH, Dyvorne H, Donnerhack C, Taouli B. Quantitative liver MRI combining phase contrast imaging, elastography, and DWI: Assessment of reproducibility and postprandial effect at 3.0 T. PLoS One 2014;9:e97355.
Rhee TK, Larson AC, Prasad PV, et al. Feasibility of blood oxygenation level-dependent MR imaging to monitor hepatic transcatheter arterial embolization in rabbits. J Vasc Interv Radiol 2005;16:1523-1528.
Burrell JS, Walker-Samuel S, Baker LC, et al. Exploring DeltaR(2) * and DeltaR(1) as imaging biomarkers of tumor oxygenation. J Magn Reson Imaging 2013;38:429-434.
Bane O, Besa C, Wagner M, et al. Feasibility and reproducibility of BOLD and TOLD measurements in the liver with oxygen and carbogen gas challenge in healthy volunteers and patients with hepatocellular carcinoma. J Magn Reson Imaging 2016;43:866-876.
Jordan BF, Misson P, Demeure R, Baudelet C, Beghein N, Gallez B. Changes in tumor oxygenation/perfusion induced by the no donor, isosorbide dinitrate, in comparison with carbogen: Monitoring by EPR and MRI. Int J Radiat Oncol Biol Phys 2000;48:565-570.
Peller M, Weissfloch L, Stehling MK, et al. Oxygen-induced MR signal changes in murine tumors. Magn Reson Imaging 1998;16:799-809.
Jhaveri KS, Cleary SP, Fischer S, et al. Blood oxygen level-dependent liver MRI: Can it predict microvascular invasion in HCC? J Magn Reson Imaging 2013;37:692-699.
Patterson AJ, Priest AN, Bowden DJ, et al. Quantitative BOLD imaging at 3T: Temporal changes in hepatocellular carcinoma and fibrosis following oxygen challenge. J Magn Reson Imaging 2016;44:739-744.
Sun D, Wei C, Shen E, Ying T, Hu B. Quantitative study of elasticity of rabbit VX2 liver tumor with alternated cooling and heating treatment based on ARFI ultrasound imaging technique. Sci Rep 2016;6:29303.
Streitberger KJ, Reiss-Zimmermann M, Freimann FB, et al. High-resolution mechanical imaging of glioblastoma by multifrequency magnetic resonance elastography. PLoS One 2014;9:e110588.
Garteiser P, Doblas S, Daire JL, et al. MR elastography of liver tumours: Value of viscoelastic properties for tumour characterisation. Eur Radiol 2012;22:2169-2177.

Auteurs

Sarah Keller (S)

Department of Radiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Julius Chapiro (J)

Department of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, Connecticut, USA.

Julia Brangsch (J)

Department of Radiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Carolin Reimann (C)

Department of Radiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Federico Collettini (F)

Department of Radiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Ingolf Sack (I)

Department of Radiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Lynn Jeanette Savic (LJ)

Department of Radiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.
Department of Radiology and Biomedical Imaging, Yale University School of Medicine, New Haven, Connecticut, USA.

Bernd Hamm (B)

Department of Radiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Shraga Nahum Goldberg (SN)

Department of Radiology, Hebrew University Hadassah Medical School, Jerusalem, Israel.

Marcus Makowski (M)

Department of Radiology, Charité - Universitätsmedizin Berlin, Berlin, Germany.

Articles similaires

1.00
Humans Yoga Low Back Pain Female Male
Humans Ketamine Propofol Pulmonary Atelectasis Female
Robotic Surgical Procedures Animals Humans Telemedicine Models, Animal

Odour generalisation and detection dog training.

Lyn Caldicott, Thomas W Pike, Helen E Zulch et al.
1.00
Animals Odorants Dogs Generalization, Psychological Smell

Classifications MeSH