Role of abbreviated MRI protocol for screening of HCC in HCV related cirrhotic patients prior to direct-acting antiviral treatment
Background Chronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC). Recent advantage of direct-acting antiviral drugs (DAA) with a high sustained virologic response (SVR) reduces overall HCV-related morbidity and...
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Published in | Egyptian Journal of Radiology and Nuclear Medicine Vol. 51; no. 1; pp. 102 - 7 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Berlin/Heidelberg
Springer Berlin Heidelberg
16.06.2020
Springer Springer Nature B.V SpringerOpen |
Subjects | |
Online Access | Get full text |
ISSN | 0378-603X 2090-4762 |
DOI | 10.1186/s43055-020-00199-x |
Cover
Abstract | Background
Chronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC). Recent advantage of direct-acting antiviral drugs (DAA) with a high sustained virologic response (SVR) reduces overall HCV-related morbidity and mortality, yet recent studies report a high recurrence rate of HCC after DAA; this calls availability of a reliable screening method to properly exclude HCC before DAA treatment.
The primary objective of our cohort study was to assess the feasibility of an abbreviated MRI protocol as a screening tool for the detection of hepatic focal lesions/early HCC in patients with HCV-related liver cirrhosis.
The study included 41 patients with HCV-related cirrhosis candidates to DAA therapy. All patients underwent routine screening for HCC by combined abdominal ultrasound and serum alfa-fetoprotein. An abbreviated MRI protocol (Abr-MR) including combined T2-weighted image and diffusion-weighted imaging (DWI) followed by dynamic contrast-enhanced MRI (CE-MRI) was performed for all subjects, assessing for presence and characterization of focal lesions.
Results
For all included 41patients, no elevation of the alpha-fetoprotein was shown. Ultrasound detected a single focal lesion in one patient. Abbreviated MR demonstrated 15 focal lesions; for detected lesions, 1 lesion shows “shine though” and the rest showing moderate and high degrees of restriction. CE-MRI characterized lesions as 1 lesion = LIRADS-1, 3 lesions = LR-M, and 11 lesions = LR-5.The standard screening using combined ultrasound and alpha-fetoprotein had sensitivity, specificity, PPV, and NPV of 6.6 % (95% CI = 0.0034–0.29), 100% (95% CI = 0.89–1.000), 100% (95% CI = 0.051–1.000), and 68.8% (95% CI = 0.54–0.80). Abr-MR protocol showed sensitivity, specificity, PPV, and NPV of 100% for all parameters (95% CI = 0.79–1.000, 0.89–1.000, 0.79–1.000, and 0.89–1.000 respectively).
Conclusion
In our study, we demonstrate the superiority of a proposed cost-effective Abr-MR protocol in the detection of hepatic focal lesions and small-sized HCC compared to routine screening using alpha-fetoprotein and ultrasound in HCV-related liver cirrhosis. |
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AbstractList | Chronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC). Recent advantage of direct-acting antiviral drugs (DAA) with a high sustained virologic response (SVR) reduces overall HCV-related morbidity and mortality, yet recent studies report a high recurrence rate of HCC after DAA; this calls availability of a reliable screening method to properly exclude HCC before DAA treatment. For all included 41patients, no elevation of the alpha-fetoprotein was shown. Ultrasound detected a single focal lesion in one patient. Abbreviated MR demonstrated 15 focal lesions; for detected lesions, 1 lesion shows "shine though" and the rest showing moderate and high degrees of restriction. CE-MRI characterized lesions as 1 lesion = LIRADS-1, 3 lesions = LR-M, and 11 lesions = LR-5.The standard screening using combined ultrasound and alpha-fetoprotein had sensitivity, specificity, PPV, and NPV of 6.6 % (95% CI = 0.0034-0.29), 100% (95% CI = 0.89-1.000), 100% (95% CI = 0.051-1.000), and 68.8% (95% CI = 0.54-0.80). Abr-MR protocol showed sensitivity, specificity, PPV, and NPV of 100% for all parameters (95% CI = 0.79-1.000, 0.89-1.000, 0.79-1.000, and 0.89-1.000 respectively). In our study, we demonstrate the superiority of a proposed cost-effective Abr-MR protocol in the detection of hepatic focal lesions and small-sized HCC compared to routine screening using alpha-fetoprotein and ultrasound in HCV-related liver cirrhosis. Background Chronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC). Recent advantage of direct-acting antiviral drugs (DAA) with a high sustained virologic response (SVR) reduces overall HCV-related morbidity and mortality, yet recent studies report a high recurrence rate of HCC after DAA; this calls availability of a reliable screening method to properly exclude HCC before DAA treatment. The primary objective of our cohort study was to assess the feasibility of an abbreviated MRI protocol as a screening tool for the detection of hepatic focal lesions/early HCC in patients with HCV-related liver cirrhosis. The study included 41 patients with HCV-related cirrhosis candidates to DAA therapy. All patients underwent routine screening for HCC by combined abdominal ultrasound and serum alfa-fetoprotein. An abbreviated MRI protocol (Abr-MR) including combined T2-weighted image and diffusion-weighted imaging (DWI) followed by dynamic contrast-enhanced MRI (CE-MRI) was performed for all subjects, assessing for presence and characterization of focal lesions. Results For all included 41patients, no elevation of the alpha-fetoprotein was shown. Ultrasound detected a single focal lesion in one patient. Abbreviated MR demonstrated 15 focal lesions; for detected lesions, 1 lesion shows "shine though" and the rest showing moderate and high degrees of restriction. CE-MRI characterized lesions as 1 lesion = LIRADS-1, 3 lesions = LR-M, and 11 lesions = LR-5.The standard screening using combined ultrasound and alpha-fetoprotein had sensitivity, specificity, PPV, and NPV of 6.6 % (95% CI = 0.0034-0.29), 100% (95% CI = 0.89-1.000), 100% (95% CI = 0.051-1.000), and 68.8% (95% CI = 0.54-0.80). Abr-MR protocol showed sensitivity, specificity, PPV, and NPV of 100% for all parameters (95% CI = 0.79-1.000, 0.89-1.000, 0.79-1.000, and 0.89-1.000 respectively). Conclusion In our study, we demonstrate the superiority of a proposed cost-effective Abr-MR protocol in the detection of hepatic focal lesions and small-sized HCC compared to routine screening using alpha-fetoprotein and ultrasound in HCV-related liver cirrhosis. Background Chronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC). Recent advantage of direct-acting antiviral drugs (DAA) with a high sustained virologic response (SVR) reduces overall HCV-related morbidity and mortality, yet recent studies report a high recurrence rate of HCC after DAA; this calls availability of a reliable screening method to properly exclude HCC before DAA treatment. The primary objective of our cohort study was to assess the feasibility of an abbreviated MRI protocol as a screening tool for the detection of hepatic focal lesions/early HCC in patients with HCV-related liver cirrhosis. The study included 41 patients with HCV-related cirrhosis candidates to DAA therapy. All patients underwent routine screening for HCC by combined abdominal ultrasound and serum alfa-fetoprotein. An abbreviated MRI protocol (Abr-MR) including combined T2-weighted image and diffusion-weighted imaging (DWI) followed by dynamic contrast-enhanced MRI (CE-MRI) was performed for all subjects, assessing for presence and characterization of focal lesions. Results For all included 41patients, no elevation of the alpha-fetoprotein was shown. Ultrasound detected a single focal lesion in one patient. Abbreviated MR demonstrated 15 focal lesions; for detected lesions, 1 lesion shows “shine though” and the rest showing moderate and high degrees of restriction. CE-MRI characterized lesions as 1 lesion = LIRADS-1, 3 lesions = LR-M, and 11 lesions = LR-5.The standard screening using combined ultrasound and alpha-fetoprotein had sensitivity, specificity, PPV, and NPV of 6.6 % (95% CI = 0.0034–0.29), 100% (95% CI = 0.89–1.000), 100% (95% CI = 0.051–1.000), and 68.8% (95% CI = 0.54–0.80). Abr-MR protocol showed sensitivity, specificity, PPV, and NPV of 100% for all parameters (95% CI = 0.79–1.000, 0.89–1.000, 0.79–1.000, and 0.89–1.000 respectively). Conclusion In our study, we demonstrate the superiority of a proposed cost-effective Abr-MR protocol in the detection of hepatic focal lesions and small-sized HCC compared to routine screening using alpha-fetoprotein and ultrasound in HCV-related liver cirrhosis. BackgroundChronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC). Recent advantage of direct-acting antiviral drugs (DAA) with a high sustained virologic response (SVR) reduces overall HCV-related morbidity and mortality, yet recent studies report a high recurrence rate of HCC after DAA; this calls availability of a reliable screening method to properly exclude HCC before DAA treatment.The primary objective of our cohort study was to assess the feasibility of an abbreviated MRI protocol as a screening tool for the detection of hepatic focal lesions/early HCC in patients with HCV-related liver cirrhosis.The study included 41 patients with HCV-related cirrhosis candidates to DAA therapy. All patients underwent routine screening for HCC by combined abdominal ultrasound and serum alfa-fetoprotein. An abbreviated MRI protocol (Abr-MR) including combined T2-weighted image and diffusion-weighted imaging (DWI) followed by dynamic contrast-enhanced MRI (CE-MRI) was performed for all subjects, assessing for presence and characterization of focal lesions.ResultsFor all included 41patients, no elevation of the alpha-fetoprotein was shown. Ultrasound detected a single focal lesion in one patient. Abbreviated MR demonstrated 15 focal lesions; for detected lesions, 1 lesion shows “shine though” and the rest showing moderate and high degrees of restriction. CE-MRI characterized lesions as 1 lesion = LIRADS-1, 3 lesions = LR-M, and 11 lesions = LR-5.The standard screening using combined ultrasound and alpha-fetoprotein had sensitivity, specificity, PPV, and NPV of 6.6 % (95% CI = 0.0034–0.29), 100% (95% CI = 0.89–1.000), 100% (95% CI = 0.051–1.000), and 68.8% (95% CI = 0.54–0.80). Abr-MR protocol showed sensitivity, specificity, PPV, and NPV of 100% for all parameters (95% CI = 0.79–1.000, 0.89–1.000, 0.79–1.000, and 0.89–1.000 respectively).ConclusionIn our study, we demonstrate the superiority of a proposed cost-effective Abr-MR protocol in the detection of hepatic focal lesions and small-sized HCC compared to routine screening using alpha-fetoprotein and ultrasound in HCV-related liver cirrhosis. Abstract Background Chronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC). Recent advantage of direct-acting antiviral drugs (DAA) with a high sustained virologic response (SVR) reduces overall HCV-related morbidity and mortality, yet recent studies report a high recurrence rate of HCC after DAA; this calls availability of a reliable screening method to properly exclude HCC before DAA treatment. The primary objective of our cohort study was to assess the feasibility of an abbreviated MRI protocol as a screening tool for the detection of hepatic focal lesions/early HCC in patients with HCV-related liver cirrhosis. The study included 41 patients with HCV-related cirrhosis candidates to DAA therapy. All patients underwent routine screening for HCC by combined abdominal ultrasound and serum alfa-fetoprotein. An abbreviated MRI protocol (Abr-MR) including combined T2-weighted image and diffusion-weighted imaging (DWI) followed by dynamic contrast-enhanced MRI (CE-MRI) was performed for all subjects, assessing for presence and characterization of focal lesions. Results For all included 41patients, no elevation of the alpha-fetoprotein was shown. Ultrasound detected a single focal lesion in one patient. Abbreviated MR demonstrated 15 focal lesions; for detected lesions, 1 lesion shows “shine though” and the rest showing moderate and high degrees of restriction. CE-MRI characterized lesions as 1 lesion = LIRADS-1, 3 lesions = LR-M, and 11 lesions = LR-5.The standard screening using combined ultrasound and alpha-fetoprotein had sensitivity, specificity, PPV, and NPV of 6.6 % (95% CI = 0.0034–0.29), 100% (95% CI = 0.89–1.000), 100% (95% CI = 0.051–1.000), and 68.8% (95% CI = 0.54–0.80). Abr-MR protocol showed sensitivity, specificity, PPV, and NPV of 100% for all parameters (95% CI = 0.79–1.000, 0.89–1.000, 0.79–1.000, and 0.89–1.000 respectively). Conclusion In our study, we demonstrate the superiority of a proposed cost-effective Abr-MR protocol in the detection of hepatic focal lesions and small-sized HCC compared to routine screening using alpha-fetoprotein and ultrasound in HCV-related liver cirrhosis. |
Audience | Professional Academic |
Author | Elia, Remon Zaher El Gaafary, Sahar Mohamed Abdulhafiz, Essam Mohamed Ahmed, Nora Nabil Abdou |
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CitedBy_id | crossref_primary_10_5114_pjr_2022_120877 crossref_primary_10_4251_wjgo_v13_i12_1919 crossref_primary_10_1016_j_jhep_2021_01_041 crossref_primary_10_1007_s11901_023_00611_w crossref_primary_10_1007_s12664_023_01511_z crossref_primary_10_3390_cancers13122975 crossref_primary_10_1111_liv_15685 crossref_primary_10_1016_j_rcl_2022_04_002 crossref_primary_10_1186_s43055_023_01083_0 crossref_primary_10_1016_j_jhep_2024_04_035 crossref_primary_10_3348_kjr_2021_0896 crossref_primary_10_1093_bjr_tqae140 crossref_primary_10_1097_HEP_0000000000000339 |
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References | ShingakiNTamaiHMoriYSerological and histological indices of hepatocellular carcinoma and tumor volume doubling timeMol Clin Oncol201319779811:CAS:528:DC%2BC3sXhvVGht77J10.3892/mco.2013.186 Nchingolo R, De Gaetano AM, Curione D et al (2014) Role of diffusion-weighted imaging, apparent diffusion coefficient and correlation with hepatobiliary phase findings in the differentiation of hepatocellular carcinoma from dysplastic nodules in cirrhotic liver. Eur Radiol PianaGTrinquartLMeskineNBarrauVBeersBVVilgrainVNew MR imaging criteria with a diffusion-weighted sequence for the diagnosis of hepatocellular carcinoma in chronic liver diseasesJ Hepatol20115512613210.1016/j.jhep.2010.10.023 LowRNGurneyJDiffusion-weighted MRI (DWI) in the oncology patient: value of breathhold DWI compared to unenhanced and gadolinium-enhanced MRIJ Magn Reson Imaging20122584885810.1002/jmri.20864 SingalAGConjeevaramHSVolkMLEffectiveness of hepatocellular carcinoma surveillance in patients with cirrhosisCancer Epidemiol Biomark Prev20122179379910.1158/1055-9965.EPI-11-1005 ZhaoXTLiWXChaiWMChenKMDetection of small hepatocellular carcinoma using gadoxetic acid-enhanced MRI: Is the addition of diffusion weighted MRI at 3.0 T beneficial?J Dig Dis2014151371451:CAS:528:DC%2BC2cXislelsLk%3D10.1111/1751-2980.1211919 KimSYAnJLimYSMRI with liver specific contrast for surveillance of patients with cirrhosis at high risk of hepatocellular carcinomaJAMA On Call20173456463 Aaron P. Thrift, Hashem B. El-Serag, Fasiha Kanwal (2017): Global epidemiology and burden of HCV infection and HCV-related disease. Nat Rev Gastroenterol Hepatol; 14:122–132. KimSYAnJLimYSHanSLeeJYByunJHWonHJLeeSJLeeHCLeeYSMRI With Liver-specific contrast for surveillance of patients with cirrhosis at high risk of hepatocellular carcinomaJAMA Oncol20173445646310.1001/jamaoncol.2016.3147 El-SeragHBEpidemiology of viral hepatitis and hepatocellular carcinomaGastroenterology20121421264127310.1053/j.gastro.2011.12.061 Singal A, Volk ML, Waljee A, Salgia R, Higgins P, Rogers MA (2009) Meta-analysis: surveillance with ultrasound for early-stage hepatocellular carcinoma in patients with cirrhosis. Aliment Pharmacol Ther:37–47 ParkMSKimSPatelJHepatocellular carcinoma: detection with diffusion-weighted versus contrast-enhanced magnetic resonance imaging in pretransplant patientsHepatology20125614014810.1002/hep.25681 TzartzevaKObiJRichNEParikhNDMarreroJASurveillance imaging and alpha fetoprotein for early detection of hepatocellular carcinoma in patients with cirrhosis: a meta-analysisGastroenterology20181546170617181:CAS:528:DC%2BC1cXosFGls78%3D10.1053/j.gastro.2018.01.064 NasuKKurokiYTsukamotoTNakajimaHMoriKMinamiMDiffusion-weighted imaging of surgically resected hepatocellular carcinoma: imaging characteristics and relationship among signal intensity, apparent diffusion coefficient, and histopathologic gradeAJR Am J Roentgenol201219343844410.2214/AJR.08.1424 ManiniMASangiovanniAFornariFPiscagliaFBiolatoMFanigliuloLClinical and economical impact of 2010 AASLD guidelines for the diagnosis of hepatocellular carcinomaJ Hepatol201460995100110.1016/j.jhep.2014.01.006 |
References_xml | – reference: SingalAGConjeevaramHSVolkMLEffectiveness of hepatocellular carcinoma surveillance in patients with cirrhosisCancer Epidemiol Biomark Prev20122179379910.1158/1055-9965.EPI-11-1005 – reference: ShingakiNTamaiHMoriYSerological and histological indices of hepatocellular carcinoma and tumor volume doubling timeMol Clin Oncol201319779811:CAS:528:DC%2BC3sXhvVGht77J10.3892/mco.2013.186 – reference: PianaGTrinquartLMeskineNBarrauVBeersBVVilgrainVNew MR imaging criteria with a diffusion-weighted sequence for the diagnosis of hepatocellular carcinoma in chronic liver diseasesJ Hepatol20115512613210.1016/j.jhep.2010.10.023 – reference: KimSYAnJLimYSMRI with liver specific contrast for surveillance of patients with cirrhosis at high risk of hepatocellular carcinomaJAMA On Call20173456463 – reference: El-SeragHBEpidemiology of viral hepatitis and hepatocellular carcinomaGastroenterology20121421264127310.1053/j.gastro.2011.12.061 – reference: TzartzevaKObiJRichNEParikhNDMarreroJASurveillance imaging and alpha fetoprotein for early detection of hepatocellular carcinoma in patients with cirrhosis: a meta-analysisGastroenterology20181546170617181:CAS:528:DC%2BC1cXosFGls78%3D10.1053/j.gastro.2018.01.064 – reference: Nchingolo R, De Gaetano AM, Curione D et al (2014) Role of diffusion-weighted imaging, apparent diffusion coefficient and correlation with hepatobiliary phase findings in the differentiation of hepatocellular carcinoma from dysplastic nodules in cirrhotic liver. Eur Radiol – reference: Aaron P. Thrift, Hashem B. El-Serag, Fasiha Kanwal (2017): Global epidemiology and burden of HCV infection and HCV-related disease. Nat Rev Gastroenterol Hepatol; 14:122–132. – reference: KimSYAnJLimYSHanSLeeJYByunJHWonHJLeeSJLeeHCLeeYSMRI With Liver-specific contrast for surveillance of patients with cirrhosis at high risk of hepatocellular carcinomaJAMA Oncol20173445646310.1001/jamaoncol.2016.3147 – reference: ZhaoXTLiWXChaiWMChenKMDetection of small hepatocellular carcinoma using gadoxetic acid-enhanced MRI: Is the addition of diffusion weighted MRI at 3.0 T beneficial?J Dig Dis2014151371451:CAS:528:DC%2BC2cXislelsLk%3D10.1111/1751-2980.1211919 – reference: LowRNGurneyJDiffusion-weighted MRI (DWI) in the oncology patient: value of breathhold DWI compared to unenhanced and gadolinium-enhanced MRIJ Magn Reson Imaging20122584885810.1002/jmri.20864 – reference: ManiniMASangiovanniAFornariFPiscagliaFBiolatoMFanigliuloLClinical and economical impact of 2010 AASLD guidelines for the diagnosis of hepatocellular carcinomaJ Hepatol201460995100110.1016/j.jhep.2014.01.006 – reference: Singal A, Volk ML, Waljee A, Salgia R, Higgins P, Rogers MA (2009) Meta-analysis: surveillance with ultrasound for early-stage hepatocellular carcinoma in patients with cirrhosis. Aliment Pharmacol Ther:37–47 – reference: NasuKKurokiYTsukamotoTNakajimaHMoriKMinamiMDiffusion-weighted imaging of surgically resected hepatocellular carcinoma: imaging characteristics and relationship among signal intensity, apparent diffusion coefficient, and histopathologic gradeAJR Am J Roentgenol201219343844410.2214/AJR.08.1424 – reference: ParkMSKimSPatelJHepatocellular carcinoma: detection with diffusion-weighted versus contrast-enhanced magnetic resonance imaging in pretransplant patientsHepatology20125614014810.1002/hep.25681 |
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Snippet | Background
Chronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC).... Background Chronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC).... Chronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC). Recent... BackgroundChronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma (HCC).... Abstract Background Chronic HCV infection is a global health problem causing progressive hepatic fibrosis, cirrhosis, and ultimately hepatocellular carcinoma... |
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SubjectTerms | Antiviral agents Antiviral drugs Cholangitis Contingency tables Contraindications Diffusion-weighted MRI Direct-acting antiviral Expected values Glycoproteins Health aspects Hepatitis C virus Hepatocellular carcinoma Imaging Infection Infections Liver Liver cancer Liver cirrhosis Magnetic resonance imaging Males Medical research Medicine Medicine & Public Health Medicine, Experimental Mortality Nuclear Medicine Patients Radiology Ultrasonic imaging Ultrasound World health |
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Title | Role of abbreviated MRI protocol for screening of HCC in HCV related cirrhotic patients prior to direct-acting antiviral treatment |
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