LI-RADS

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LI-RADS
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LIRADS classification is applied to multi-phase contrast-enhanced CT or MRI scans in people with certain chronic liver diseases.
Synonyms Liver Reporting & Data System

The Liver Imaging Reporting and Data System (aka LI-RADS) is a quality assurance tool created and trademarked by the American College of Radiology in 2011 to standardize the reporting and data collection of CT and MR imaging patients at risk for hepatocellular carcinoma (HCC), or primary cancer of the liver cells. [1] It provides a standardized framework for classification of liver lesions by a radiologist, and only applies in patients with chronic liver disease, the main risk factor for liver cancer. The hierarchical classification, from LR1 to LR5, is based on specific imaging features of the lesion in question, and corresponds to the degree of suspicion for malignancy. For example, a lesion with features corresponding to the highest category, LR5, is "definitely" HCC. Importantly, the increasing acceptance of the LI-RADS system of reporting by referring clinicians (chiefly oncologists, hepatobiliary and liver transplant surgeons) has reduced the need for tissue biopsy confirmation of cancer in patients with chronic liver disease.

Contents

The LI-RADS system has undergone two revisions, first in 2014, [2] and again in July 2018. [3]

In 2016, the ACR published a version of LI-RADS which applies to contrast-enhanced ultrasound imaging, termed CEUS LI-RADS. [1]

LI-RADS 2018 Version

LI-RADS v2018 makes some slight changes on the classification, improving the sensitivity of detecting small HCC (1~2cm) [4]

Role of LI-RADS in liver transplantation

The only potential curative treatment for hepatocellular carcinoma, assuming that the disease has not spread beyond the liver, is surgically removing the tumor from the body. In some cases, if the tumor is limited and the patient is healthy enough to tolerate surgery, the tumor may be successfully treated by resecting the affected part of the liver (partial hepatectomy). If the person is not a good candidate for surgical resection due advanced liver disease (commonly by Child-Pugh score), liver transplantation may still be a curative treatment option. Provided that the disease has not spread beyond the liver, then liver transplant effectively removes all cancer cells from the body, while also replacing the disease native liver with a better functioning transplant organ.

Liver transplantation has significant risks, including the risk of recurrent cancer. The outcomes and survival benefits of transplantation as treatment of HCC are highest when transplant is reserved for the "best" candidates which meet strict criteria. In addition to undergoing a complete medical and psychological evaluation, imaging assessment for extent of the cancer is an important component of eligibility for transplant. A landmark study in 1996 showed that both overall and recurrence-free survival following liver transplantation for cirrhosis and unresectable HCC was improved by limiting this treatment to disease that met certain strict criteria, now known as the Milan criteria. [5] The criteria include assessment of size and number of active liver tumors, as well as the absence of invasion of large blood vessels. In the U.S., these Milan criteria are currently used by the Organ Procurement and Transplantation Network (OPTN) committee to evaluate transplant candidacy. [6] Only persons with limited disease, as defined by the criteria, are considered for transplantation.

Potential candidates for liver transplantation for treatment of HCC are evaluated and re-evaluated periodically by repeated imaging tests as they wait for donor organ availability. So long as the cancer does not exceed Milan criteria, the person may remain a candidate for transplantation. Thus, accurate and consistent evaluation of the disease burden is critical. For example, if someone with three small HCC lesions develops a new fourth liver nodule, an unequivocal diagnosis of this lesion as cancerous would disqualify this person from transplant candidacy.

The 5 tiers of the LI-RADS reporting system are designed to correspond to the 5 tier classification recommended by the United Network for Organ Sharing (UNOS) which administers OPTN. [6] For all intents and purposes, OPTN/UNOS classes 1-5 correspond to LI-RADS 1-5 classification, although there are some small differences:

Although there are 5 levels of classification, the most significant and only actionable classification is LI-RADS or OPTN/UNOS 5, which indicates that a nodule is "definitely" cancer. The UNOS-OPTN recommendations to not provide guidance on liver nodules which do not meet this strict criteria for malignancy.

Automatic extraction using Machine Learning

Natural language processing tool [7] available for computation of LI-RADS assessment category from the findings recorded in the textual radiology reports (documented without LI-RADS template) which may enable standardizing screening recommendations and treatment planning of patients at risk for hepatocellular carcinoma by using same scoring criteria. In addition, such system may facilitate AI-based healthcare research with images by offering large scale text mining and data gathering opportunities from standard hospital clinical data repositories.

Related Research Articles

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Hepatocellular carcinoma (HCC) is the most common type of primary liver cancer in adults and is currently the most common cause of death in people with cirrhosis. HCC is the third leading cause of cancer-related deaths worldwide.

Liver tumors are abnormal growth of liver cells on or in the liver. Several distinct types of tumors can develop in the liver because the liver is made up of various cell types. Liver tumors can be classified as benign (non-cancerous) or malignant (cancerous) growths. They may be discovered on medical imaging, and the diagnosis is often confirmed with liver biopsy. Signs and symptoms of liver masses vary from being asymptomatic to patients presenting with an abdominal mass, hepatomegaly, abdominal pain, jaundice, or some other liver dysfunction. Treatment varies and is highly specific to the type of liver tumor.

<span class="mw-page-title-main">Renal cell carcinoma</span> Medical condition

Renal cell carcinoma (RCC) is a kidney cancer that originates in the lining of the proximal convoluted tubule, a part of the very small tubes in the kidney that transport primary urine. RCC is the most common type of kidney cancer in adults, responsible for approximately 90–95% of cases. RCC occurrence shows a male predominance over women with a ratio of 1.5:1. RCC most commonly occurs between 6th and 7th decade of life.

<span class="mw-page-title-main">Interventional radiology</span> Medical subspecialty

Interventional radiology (IR) is a medical specialty that performs various minimally-invasive procedures using medical imaging guidance, such as x-ray fluoroscopy, computed tomography, magnetic resonance imaging, or ultrasound. IR performs both diagnostic and therapeutic procedures through very small incisions or body orifices. Diagnostic IR procedures are those intended to help make a diagnosis or guide further medical treatment, and include image-guided biopsy of a tumor or injection of an imaging contrast agent into a hollow structure, such as a blood vessel or a duct. By contrast, therapeutic IR procedures provide direct treatment—they include catheter-based medicine delivery, medical device placement, and angioplasty of narrowed structures.

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In oncology, AFP-L3 is an isoform of alpha-fetoprotein (AFP), a substance typically used in the triple test during pregnancy and for screening chronic liver disease patients for hepatocellular carcinoma (HCC). AFP can be fractionated by affinity electrophoresis into three glycoforms: L1, L2, and L3 based on the reactivity with the lectin Lens culinaris agglutinin (LCA). AFP-L3 binds strongly to LCA via an additional α 1-6 fucose residue attached at the reducing terminus of N-acetylglucosamine; this is in contrast to the L1 isoform. It is the L1 isoform which is typically associated with non-HCC inflammation of liver disease condition. The L3 isoform is specific to malignant tumors and its detected presence can serve to identify patients whom need increased monitoring for the development of HCC in high risk populations. AFP-L3% is now being considered as a tumor marker for the North American demographic.

Response evaluation criteria in solid tumors (RECIST) is a set of published rules that define when tumors in cancer patients improve ("respond"), stay the same ("stabilize"), or worsen ("progress") during treatment. The criteria were published in February 2000 by an international collaboration including the European Organisation for Research and Treatment of Cancer (EORTC), National Cancer Institute of the United States, and the National Cancer Institute of Canada Clinical Trials Group. Today, the majority of clinical trials evaluating cancer treatments for objective response in solid tumors use RECIST. These criteria were developed and published in February 2000, and subsequently updated in 2009.

Des-gamma carboxyprothrombin (DCP), also known as protein induced by vitamin K absence/antagonist-II (PIVKA-II), is an abnormal form of the coagulation protein, prothrombin. Normally, the prothrombin precursor undergoes post-translational carboxylation by gamma-glutamyl carboxylase in the liver prior to secretion into plasma. DCP/PIVKA-II may be detected in people with deficiency of vitamin K and in those taking warfarin or other medication that inhibits the action of vitamin K.

<span class="mw-page-title-main">Liver cancer</span> Medical condition

Liver cancer is cancer that starts in the liver. Liver cancer can be primary or secondary. Liver metastasis is more common than that which starts in the liver. Liver cancer is increasing globally.

TheraSphere is a radiotherapy treatment for hepatocellular carcinoma (HCC) that consists of millions of microscopic, radioactive glass microspheres being infused into the arteries that feed liver tumors. These microspheres then embolize, lodging themselves in the liver's capillaries and bathing the malignancy in high levels of yttrium-90 radiation. It is currently approved as a Humanitarian Device, meaning effectiveness has not been proven, for patients as a neoadjuvant to surgery or transplantation by the U.S. Food and Drug Administration and is being used at a number of clinical centers in the United States.

<span class="mw-page-title-main">Thyroid nodule</span> Medical condition

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<span class="mw-page-title-main">Fibrolamellar hepatocellular carcinoma</span> Medical condition

Fibrolamellar carcinoma (FLC) is a rare form of carcinoma that typically affects young adults and is characterized, under the microscope, by laminated fibrous layers interspersed between the tumor cells. It has been estimated that 200 new cases are diagnosed worldwide each year. However, in light of recent advances in our molecular understanding, this has recently been revised to suggest it may be at least ten times more common. FLC, also known as fibrolamellar hepatocellular carcinoma, is different from the more common hepatocellular carcinoma (HCC) in that it afflicts young people with normal liver function and no known risk factors.

<span class="mw-page-title-main">Selective internal radiation therapy</span>

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Ultrasonography of liver tumors involves two stages: detection and characterization.

Transarterial bland embolization is a catheter-based tumor treatment of the liver. In this procedure, embolizing agents can be delivered through the tumor’s feeding artery in order to completely occlude the tumor’s blood supply. The anti-tumor effects are solely based on tumor ischemia and infarction of tumor tissue, as no chemotherapeutic agents are administered. The rationale for the use of bland embolization for hepatocellular carcinoma (HCC) and/or other hyper-vascular tumors is based on the fact that a normal liver receives a dual blood supply from the hepatic artery (25%) and the portal vein (75%). As the tumor grows, it becomes increasingly dependent on the hepatic artery for blood supply. Once a tumor nodule reaches a diameter of 2 cm or more, most of the blood supply is derived from the hepatic artery. Therefore, bland embolization and transarterial chemoembolization (TACE) consist of the selective angiographic occlusion of the tumor arterial blood supply with a variety of embolizing agents, with or without the precedence of local chemotherapy infusion. The occlusion by embolic particles results in tumor hypoxia and necrosis, without affecting the normal hepatic parenchyma.

References

  1. 1 2 "Liver Imaging Reporting and Data System". ACR.org. American College of Radiology. Retrieved 19 February 2017.
  2. "LI-RADS v2014". American College of Radiology. Retrieved 2017-07-09.
  3. "CT/MRI LI-RADS® v2017". American College of Radiology. Retrieved 2017-07-09.
  4. Lee, Sang Min; Lee, Jeong Min; Ahn, Su Joa; Kang, Hyo-Jin; Yang, Hyun Kyung; Yoon, Jeong Hee (16 July 2019). "LI-RADS Version 2017 versus Version 2018: Diagnosis of Hepatocellular Carcinoma on Gadoxetate Disodium–enhanced MRI". Radiology. 292 (3): 655–663. doi:10.1148/radiol.2019182867. ISSN   0033-8419. PMID   31310175. S2CID   196811464.
  5. Mazzaferro, Vincenzo; Regalia, Enrico; Doci, Roberto; Andreola, Salvatore; Pulvirenti, Andrea; Bozzetti, Federico; Montalto, Fabrizio; Ammatuna, Mario; Morabito, Alberto (1996-03-14). "Liver Transplantation for the Treatment of Small Hepatocellular Carcinomas in Patients with Cirrhosis". New England Journal of Medicine. 334 (11): 693–700. doi: 10.1056/nejm199603143341104 . ISSN   0028-4793. PMID   8594428.
  6. 1 2 Wald, Christoph; Russo, Mark W.; Heimbach, Julie K.; Hussain, Hero K.; Pomfret, Elizabeth A.; Bruix, Jordi (2013-02-01). "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. ISSN   0033-8419. PMID   23362092.
  7. Banerjee, Imon; Choi, Hailye H.; Desser, Terry; Rubin, Daniel L. (2018). "A Scalable Machine Learning Approach for Inferring Probabilistic US-LI-RADS Categorization". AMIA ... Annual Symposium Proceedings. AMIA Symposium. 2018: 215–224. ISSN   1942-597X. PMC   6371287 . PMID   30815059.