A Narrative Review on LI-RADS Algorithm in Liver Tumors: Prospects and Pitfalls
Liver cancer is the sixth most detected tumor and the third leading cause of tumor death worldwide. Hepatocellular carcinoma (HCC) is the most common primary liver malignancy with specific risk factors and a targeted population. Imaging plays a major role in the management of HCC from screening to p...
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| Published in | Diagnostics (Basel) Vol. 12; no. 7; p. 1655 |
|---|---|
| Main Authors | , , , , , , , , , , , , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Switzerland
MDPI AG
07.07.2022
MDPI |
| Subjects | |
| Online Access | Get full text |
| ISSN | 2075-4418 2075-4418 |
| DOI | 10.3390/diagnostics12071655 |
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| Abstract | Liver cancer is the sixth most detected tumor and the third leading cause of tumor death worldwide. Hepatocellular carcinoma (HCC) is the most common primary liver malignancy with specific risk factors and a targeted population. Imaging plays a major role in the management of HCC from screening to post-therapy follow-up. In order to optimize the diagnostic-therapeutic management and using a universal report, which allows more effective communication among the multidisciplinary team, several classification systems have been proposed over time, and LI-RADS is the most utilized. Currently, LI-RADS comprises four algorithms addressing screening and surveillance, diagnosis on computed tomography (CT)/magnetic resonance imaging (MRI), diagnosis on contrast-enhanced ultrasound (CEUS) and treatment response on CT/MRI. The algorithm allows guiding the radiologist through a stepwise process of assigning a category to a liver observation, recognizing both major and ancillary features. This process allows for characterizing liver lesions and assessing treatment. In this review, we highlighted both major and ancillary features that could define HCC. The distinctive dynamic vascular pattern of arterial hyperenhancement followed by washout in the portal-venous phase is the key hallmark of HCC, with a specificity value close to 100%. However, the sensitivity value of these combined criteria is inadequate. Recent evidence has proven that liver-specific contrast could be an important tool not only in increasing sensitivity but also in diagnosis as a major criterion. Although LI-RADS emerges as an essential instrument to support the management of liver tumors, still many improvements are needed to overcome the current limitations. In particular, features that may clearly distinguish HCC from cholangiocarcinoma (CCA) and combined HCC-CCA lesions and the assessment after locoregional radiation-based therapy are still fields of research. |
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| AbstractList | Liver cancer is the sixth most detected tumor and the third leading cause of tumor death worldwide. Hepatocellular carcinoma (HCC) is the most common primary liver malignancy with specific risk factors and a targeted population. Imaging plays a major role in the management of HCC from screening to post-therapy follow-up. In order to optimize the diagnostic-therapeutic management and using a universal report, which allows more effective communication among the multidisciplinary team, several classification systems have been proposed over time, and LI-RADS is the most utilized. Currently, LI-RADS comprises four algorithms addressing screening and surveillance, diagnosis on computed tomography (CT)/magnetic resonance imaging (MRI), diagnosis on contrast-enhanced ultrasound (CEUS) and treatment response on CT/MRI. The algorithm allows guiding the radiologist through a stepwise process of assigning a category to a liver observation, recognizing both major and ancillary features. This process allows for characterizing liver lesions and assessing treatment. In this review, we highlighted both major and ancillary features that could define HCC. The distinctive dynamic vascular pattern of arterial hyperenhancement followed by washout in the portal-venous phase is the key hallmark of HCC, with a specificity value close to 100%. However, the sensitivity value of these combined criteria is inadequate. Recent evidence has proven that liver-specific contrast could be an important tool not only in increasing sensitivity but also in diagnosis as a major criterion. Although LI-RADS emerges as an essential instrument to support the management of liver tumors, still many improvements are needed to overcome the current limitations. In particular, features that may clearly distinguish HCC from cholangiocarcinoma (CCA) and combined HCC-CCA lesions and the assessment after locoregional radiation-based therapy are still fields of research. Liver cancer is the sixth most detected tumor and the third leading cause of tumor death worldwide. Hepatocellular carcinoma (HCC) is the most common primary liver malignancy with specific risk factors and a targeted population. Imaging plays a major role in the management of HCC from screening to post-therapy follow-up. In order to optimize the diagnostic-therapeutic management and using a universal report, which allows more effective communication among the multidisciplinary team, several classification systems have been proposed over time, and LI-RADS is the most utilized. Currently, LI-RADS comprises four algorithms addressing screening and surveillance, diagnosis on computed tomography (CT)/magnetic resonance imaging (MRI), diagnosis on contrast-enhanced ultrasound (CEUS) and treatment response on CT/MRI. The algorithm allows guiding the radiologist through a stepwise process of assigning a category to a liver observation, recognizing both major and ancillary features. This process allows for characterizing liver lesions and assessing treatment. In this review, we highlighted both major and ancillary features that could define HCC. The distinctive dynamic vascular pattern of arterial hyperenhancement followed by washout in the portal-venous phase is the key hallmark of HCC, with a specificity value close to 100%. However, the sensitivity value of these combined criteria is inadequate. Recent evidence has proven that liver-specific contrast could be an important tool not only in increasing sensitivity but also in diagnosis as a major criterion. Although LI-RADS emerges as an essential instrument to support the management of liver tumors, still many improvements are needed to overcome the current limitations. In particular, features that may clearly distinguish HCC from cholangiocarcinoma (CCA) and combined HCC-CCA lesions and the assessment after locoregional radiation-based therapy are still fields of research. Liver cancer is the sixth most detected tumor and the third leading cause of tumor death worldwide. Hepatocellular carcinoma (HCC) is the most common primary liver malignancy with specific risk factors and a targeted population. Imaging plays a major role in the management of HCC from screening to post-therapy follow-up. In order to optimize the diagnostic-therapeutic management and using a universal report, which allows more effective communication among the multidisciplinary team, several classification systems have been proposed over time, and LI-RADS is the most utilized. Currently, LI-RADS comprises four algorithms addressing screening and surveillance, diagnosis on computed tomography (CT)/magnetic resonance imaging (MRI), diagnosis on contrast-enhanced ultrasound (CEUS) and treatment response on CT/MRI. The algorithm allows guiding the radiologist through a stepwise process of assigning a category to a liver observation, recognizing both major and ancillary features. This process allows for characterizing liver lesions and assessing treatment. In this review, we highlighted both major and ancillary features that could define HCC. The distinctive dynamic vascular pattern of arterial hyperenhancement followed by washout in the portal-venous phase is the key hallmark of HCC, with a specificity value close to 100%. However, the sensitivity value of these combined criteria is inadequate. Recent evidence has proven that liver-specific contrast could be an important tool not only in increasing sensitivity but also in diagnosis as a major criterion. Although LI-RADS emerges as an essential instrument to support the management of liver tumors, still many improvements are needed to overcome the current limitations. In particular, features that may clearly distinguish HCC from cholangiocarcinoma (CCA) and combined HCC-CCA lesions and the assessment after locoregional radiation-based therapy are still fields of research.Liver cancer is the sixth most detected tumor and the third leading cause of tumor death worldwide. Hepatocellular carcinoma (HCC) is the most common primary liver malignancy with specific risk factors and a targeted population. Imaging plays a major role in the management of HCC from screening to post-therapy follow-up. In order to optimize the diagnostic-therapeutic management and using a universal report, which allows more effective communication among the multidisciplinary team, several classification systems have been proposed over time, and LI-RADS is the most utilized. Currently, LI-RADS comprises four algorithms addressing screening and surveillance, diagnosis on computed tomography (CT)/magnetic resonance imaging (MRI), diagnosis on contrast-enhanced ultrasound (CEUS) and treatment response on CT/MRI. The algorithm allows guiding the radiologist through a stepwise process of assigning a category to a liver observation, recognizing both major and ancillary features. This process allows for characterizing liver lesions and assessing treatment. In this review, we highlighted both major and ancillary features that could define HCC. The distinctive dynamic vascular pattern of arterial hyperenhancement followed by washout in the portal-venous phase is the key hallmark of HCC, with a specificity value close to 100%. However, the sensitivity value of these combined criteria is inadequate. Recent evidence has proven that liver-specific contrast could be an important tool not only in increasing sensitivity but also in diagnosis as a major criterion. Although LI-RADS emerges as an essential instrument to support the management of liver tumors, still many improvements are needed to overcome the current limitations. In particular, features that may clearly distinguish HCC from cholangiocarcinoma (CCA) and combined HCC-CCA lesions and the assessment after locoregional radiation-based therapy are still fields of research. |
| Audience | Academic |
| Author | Danti, Ginevra Simonetti, Igino Agostini, Andrea Barile, Antonio Flammia, Federica Granata, Vincenza Grassi, Roberta Miele, Vittorio Bruno, Federico Chiti, Giuditta De Muzio, Federica Giovagnoni, Andrea Grassi, Francesca Palumbo, Pierpaolo Dell’Aversana, Federica Valeri, Tommaso Fusco, Roberta Cutolo, Carmen |
| AuthorAffiliation | 11 Radiology Division, Istituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, Via Mariano Semmola, 80131 Naples, Italy; igino.simonetti@istitutotumori.na.it (I.S.); v.granata@istitutotumori.na.it (V.G.) 7 Department of Radiological Sciences, University Hospital Ospedali Riuniti, Via Tronto 10/a, 60126 Torrette, Italy 8 Area of Cardiovascular and Interventional Imaging, Department of Diagnostic Imaging, Abruzzo Health Unit 1, 67100 L’Aquila, Italy 2 Division of Radiology, Università degli Studi della Campania Luigi Vanvitelli, 81100 Naples, Italy; francesca.grassi1@studenti.unicampania.it (F.G.); federica.dellaversana@studenti.unicampania.it (F.D.); roberta.grassi@policliniconapoli.it (R.G.) 4 Division of Radiology, Azienda Ospedaliera Universitaria Careggi, 50134 Florence, Italy; ginevra.danti@gmail.com (G.D.); federicaflammia91@gmail.com (F.F.); giudittachiti@gmail.com (G.C.); vmiele@sirm.org (V.M.) 5 Italian Society of Medical and Interventional Radiology (SIRM), SIRM Foundation, 20122 Mi |
| AuthorAffiliation_xml | – name: 2 Division of Radiology, Università degli Studi della Campania Luigi Vanvitelli, 81100 Naples, Italy; francesca.grassi1@studenti.unicampania.it (F.G.); federica.dellaversana@studenti.unicampania.it (F.D.); roberta.grassi@policliniconapoli.it (R.G.) – name: 8 Area of Cardiovascular and Interventional Imaging, Department of Diagnostic Imaging, Abruzzo Health Unit 1, 67100 L’Aquila, Italy – name: 3 Medical Oncology Division, Igea SpA, 80013 Naples, Italy – name: 9 Emergency Radiology, San Salvatore Hospital, Via Lorenzo Natali 1, 67100 L’Aquila, Italy; abarile63@gmail.com – name: 1 Department of Medicine and Health Sciences V. Tiberio, University of Molise, 86100 Campobasso, Italy; demuziofederica@gmail.com – name: 6 Department of Clinical Special and Dental Sciences, University Politecnica delle Marche, 60126 Ancona, Italy; t.valeri@univpm.it (T.V.); a.agostini@staff.univpm.it (A.A.); a.giovagnoni@univpm.it (A.G.) – name: 5 Italian Society of Medical and Interventional Radiology (SIRM), SIRM Foundation, 20122 Milan, Italy; palumbopierpaolo89@gmail.com (P.P.); federico.bruno.1988@gmail.com (F.B.) – name: 7 Department of Radiological Sciences, University Hospital Ospedali Riuniti, Via Tronto 10/a, 60126 Torrette, Italy – name: 4 Division of Radiology, Azienda Ospedaliera Universitaria Careggi, 50134 Florence, Italy; ginevra.danti@gmail.com (G.D.); federicaflammia91@gmail.com (F.F.); giudittachiti@gmail.com (G.C.); vmiele@sirm.org (V.M.) – name: 11 Radiology Division, Istituto Nazionale Tumori-IRCCS-Fondazione G. Pascale, Via Mariano Semmola, 80131 Naples, Italy; igino.simonetti@istitutotumori.na.it (I.S.); v.granata@istitutotumori.na.it (V.G.) – name: 10 Department of Medicine, Surgery and Dentistry, University of Salerno, 84084 Fisciano, Italy; carmencutolo@hotmail.it |
| Author_xml | – sequence: 1 givenname: Federica surname: De Muzio fullname: De Muzio, Federica – sequence: 2 givenname: Francesca surname: Grassi fullname: Grassi, Francesca – sequence: 3 givenname: Federica surname: Dell’Aversana fullname: Dell’Aversana, Federica – sequence: 4 givenname: Roberta surname: Fusco fullname: Fusco, Roberta – sequence: 5 givenname: Ginevra orcidid: 0000-0002-7109-8119 surname: Danti fullname: Danti, Ginevra – sequence: 6 givenname: Federica surname: Flammia fullname: Flammia, Federica – sequence: 7 givenname: Giuditta surname: Chiti fullname: Chiti, Giuditta – sequence: 8 givenname: Tommaso surname: Valeri fullname: Valeri, Tommaso – sequence: 9 givenname: Andrea surname: Agostini fullname: Agostini, Andrea – sequence: 10 givenname: Pierpaolo orcidid: 0000-0003-1514-0092 surname: Palumbo fullname: Palumbo, Pierpaolo – sequence: 11 givenname: Federico orcidid: 0000-0002-1444-2585 surname: Bruno fullname: Bruno, Federico – sequence: 12 givenname: Carmen surname: Cutolo fullname: Cutolo, Carmen – sequence: 13 givenname: Roberta surname: Grassi fullname: Grassi, Roberta – sequence: 14 givenname: Igino surname: Simonetti fullname: Simonetti, Igino – sequence: 15 givenname: Andrea surname: Giovagnoni fullname: Giovagnoni, Andrea – sequence: 16 givenname: Vittorio orcidid: 0000-0002-7848-1567 surname: Miele fullname: Miele, Vittorio – sequence: 17 givenname: Antonio orcidid: 0000-0003-0253-3583 surname: Barile fullname: Barile, Antonio – sequence: 18 givenname: Vincenza orcidid: 0000-0002-6601-3221 surname: Granata fullname: Granata, Vincenza |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/35885561$$D View this record in MEDLINE/PubMed |
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| SubjectTerms | Algorithms Cholangiocarcinoma Clinical medicine Cysts Diagnosis Diagnosis, Differential Evaluation Hepatitis Hepatoma LI-RADS liver Liver cancer Liver diseases Magnetic resonance imaging Medical screening Methods Patients Radiology Radiology, Medical Review Surveillance Ultrasonic imaging Working groups |
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| Title | A Narrative Review on LI-RADS Algorithm in Liver Tumors: Prospects and Pitfalls |
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