Contrast-enhanced ultrasound Liver Imaging Reporting and Data System: Lights and shadows in hepatocellular carcinoma and cholangiocellular carcinoma diagnosis

Abstract

BACKGROUND

Contrast-enhanced ultrasound (CEUS) is considered a secondary examination compared to computed tomography (CT) and magnetic resonance imaging (MRI) in the diagnosis of hepatocellular carcinoma (HCC), due to the risk of misdiagnosing intrahepatic cholangiocarcinoma (ICC). The introduction of CEUS Liver Imaging Reporting and Data System (CEUS LI-RADS) might overcome this limitation. Even though data from the literature seems promising, its reliability in real-life context has not been well-established yet.

AIM

To test the accuracy of CEUS LI-RADS for correctly diagnosing HCC and ICC in cirrhosis.

METHODS

CEUS LI-RADS class was retrospectively assigned to 511 nodules identified in 269 patients suffering from liver cirrhosis. The diagnostic standard for all nodules was either biopsy (102 nodules) or CT/MRI (409 nodules). Common diagnostic accuracy indexes such as sensitivity, specificity, positive predictive value (PPV), and negative predictive value (NPV) were assessed for the following associations: CEUS LR-5 and HCC; CEUS LR-4 and 5 merged class and HCC; CEUS LR-M and ICC; and CEUS LR-3 and malignancy. The frequency of malignant lesions in CEUS LR-3 subgroups with different CEUS patterns was also determined. Inter-rater agreement for CEUS LI-RADS class assignment and for major CEUS pattern identification was evaluated.

RESULTS

CEUS LR-5 predicted HCC with a 67.6% sensitivity, 97.7% specificity, and 99.3% PPV (P < 0.001). The merging of LR-4 and 5 offered an improved 93.9% sensitivity in HCC diagnosis with a 94.3% specificity and 98.8% PPV (P < 0.001). CEUS LR-M predicted ICC with a 91.3% sensitivity, 96.7% specificity, and 99.6% NPV (P < 0.001). CEUS LR-3 predominantly included benign lesions (only 28.8% of malignancies). In this class, the hypo-hypo pattern showed a much higher rate of malignant lesions (73.3%) than the iso-iso pattern (2.6%). Inter-rater agreement between internal raters for CEUS-LR class assignment was almost perfect (n = 511, k = 0.94, P < 0.001), while the agreement among raters from separate centres was substantial (n = 50, k = 0.67, P < 0.001). Agreement was stronger for arterial phase hyperenhancement (internal k = 0.86, P < 2.7 × 10^-214; external k = 0.8, P < 0.001) than washout (internal k = 0.79, P < 1.6 × 10^-202; external k = 0.71, P < 0.001).

CONCLUSION

CEUS LI-RADS is effective but can be improved by merging LR-4 and 5 to diagnose HCC and by splitting LR-3 into two subgroups to differentiate iso-iso nodules from other patterns.

Key Words: Contrast-enhanced ultrasound Liver Imaging Reporting and Data System, Hepatocellular carcinoma, Intrahepatic cholangiocarcinoma, Cirrhosis, Contrast-enhanced ultrasound, Liver

Core Tip: This is a retrospective study to evaluate the accuracy of contrast-enhanced ultrasound Liver Imaging Reporting and Data System (CEUS LI-RADS) in correctly diagnosing hepatocellular carcinoma (HCC) and intrahepatic cholangiocarcinoma (ICC) in patients with cirrhosis. CEUS LR-5 showed a 97.7% specificity for HCC with a low sensitivity (67.6%), while the CEUS LR-4 and 5 merged class showed a 93.9% sensitivity and 94.3% specificity for HCC. CEUS LR-M predicted ICC with a 91.3% sensitivity and 96.7% specificity. CEUS LR-3 predominantly included benign lesions (28.8% of malignancies) but was heterogeneous as the hypo-hypo pattern showed a higher rate of malignant lesions (73.3%) than the iso-iso pattern (2.6%).

INTRODUCTION

Liver cirrhosis is a strong risk factor for primitive liver cancer, the seventh most commonly diagnosed malignancy worldwide and the third most common cause of cancer-related death[1]. In this scenario, the most prevalent malignant lesion is hepatocellular carcinoma (HCC), followed by intrahepatic cholangiocarcinoma (ICC); however, other types of cancer are rare. The development of a malignant lesion represents a critical point in the clinical history of chronic liver diseases since it significantly reduces life expectancy, especially in case of late diagnosis. Therefore, regular follow-up is essential for these patients with mandatory ultrasonography every 6 mo for detecting solid focal liver lesions[2-5].

Contrast-enhanced ultrasound (CEUS) is an effective, well-recognized, and safe imaging technique for visualising the onset of new nodules in liver cirrhosis, that adheres to national and international guidelines[2,6,7]. One of the initial limitations of CEUS, reported in 2010, was the possibility of missing ICC cases, since a significant proportion of the ICC nodules that develop in a cirrhotic liver show the same enhancement pattern as HCC[8]. Since then, subsequent studies have demonstrated that the timing and intensity of washout are different in HCC and ICC. In particular, for the vast majority of ICC nodules (50%-85%), washout starts earlier than 60 s, while this is rarely observed in HCC. Furthermore, washout intensity during late phase is clearer in ICC than in HCC[9-14]. These findings led the American College of Radiology to release the CEUS Liver Imaging Reporting and Data System (CEUS LI-RADS), similar to previous releases for computed tomography (CT) and magnetic resonance imaging (MRI). The algorithm was officially approved in June 2016, and the latest update was published in 2017[15].

CEUS LI-RADS is a standardized system for technique, interpretation, reporting, and data collection on focal liver lesions in patients at high risk for HCC. It encompasses features such as size, conventional ultrasound morphology, contrast enhancement behaviours, and dimensional variations in order to stratify the risk of HCC and to avoid ICC misdiagnosis[16-20]. In particular, CEUS LR-5 is a class specifically designed to include HCC. It encompasses nodules > 1 cm that show arterial phase hyperenhancement (APHE) that is neither rim nor globular, followed by a late (> 60 s) mild-degree washout. Other CEUS LI-RADS categories (e.g., CEUS LR-4 and 3) express a very probable and intermediate risk of HCC, while CEUS LR-M has an intermediate/high risk of malignancy without a typical HCC pattern. CEUS LR-M includes lesions of any size that show arterial phase rim enhancement pattern and/or early (before 60 s) washout and/or marked washout.

So far, only a few studies have presented actual data from the application of CEUS LI-RADS diagnostic algorithm in cirrhotic patients with suspicious nodules[21-27]. The aim of this study was to test the capability of CEUS LI-RADS in accurately diagnosing focal liver lesions in patients affected by cirrhosis. In particular, we tested the accuracy of CEUS LR-5 and LR-M in correctly diagnosing HCC and ICC, respectively. In addition, we merged classes LR-4 and LR-5 and tested their accuracy in correctly diagnosing HCC as a joint class. Finally, we assessed the rate of malignancy for specific LR-3 class patterns.

MATERIALS AND METHODS

Study design and data collection

The present retrospective study involved patients with cirrhosis associated nodules that were visible using conventional ultrasound, for which it was possible to review the basal appearance and dynamic pattern of the ultrasound contrast agent. Cirrhosis was diagnosed on the basis of clinical data, biochemical parameters, imaging criteria, and elastosonography.

We reviewed all the liver CEUS performed at our centre (Medical Ultrasound Unit, University Hospital, Sassari, Italy) between December 2008 and January 2020. All examinations aimed to characterize a new nodule developed in the context of surveillance programmes for liver cirrhosis. Nodules located in different liver segments were analysed separately with individual boluses of contrast. Within the same segment, only one target nodule was included for analysis based on best visualization criteria.

CT and/or MRI, when typical for HCC or definitely benign (haemangioma, hepatic fat deposition/sparing, and hypertrophic pseudomass), were used as the gold standard imaging modalities. For all other cases, histology obtained by a percutaneous biopsy or surgical resection was considered the reference standard (Supplementary Figures 1 and 2).

Specifically, nodules showing a CT/MRI dynamic pattern with hyperenhancement during the arterial phase followed by washout in the portal or late phase (Supplementary Figures 3 and 4), were diagnosed as HCC in accordance with both the American Association for the Study of Liver Diseases (AASLD) and the Italian Association for the Study of the Liver (AISF) guidelines[2,28]. Benign lesions received a further 2-year follow-up; in case of any increase in size and/or CEUS enhancement variations, a biopsy was performed.

All cases where it was not possible to review the timing and the degree of washout on CEUS (23 cases), or a validated diagnostic reference standard, either CT/MRI scan or histology, was not available (35 cases), were excluded. The algorithm of the study is shown in Figure 1.

Figure 1  Flow chart of the study.

CEUS examination and CEUS LI-RADS classification

All CEUS examinations were performed by a physician with 15 years of experience (G.V.) using a second-generation ultrasound contrast agent (SonoVue, Bracco, Milan, Italy).

The signal coming from the bubbles was detected through the following ultrasound scanners: (1) Acuson Sequoia 512 with a 4C1 convex probe and cadence contrast pulse sequencing (CPS, Acuson Siemens, Mountain View, CA, United States) until 2014; and (2) Aixplorer (SuperSonic Imaging, S.A., Aix en Provence, France) with a convex broadband probe (SC6-1) and dedicated software also known as Power Modulated Pulse Inversion (PMPI) from January 2015 until the end of the study.

The CEUS examination was performed continuously for 120 s starting from the injection of contrast. Subsequently, short clips lasting 15-30 s were recorded until 5 min after injection.

The CEUS LI-RADS patterns were established after evaluation of all clips and images, with particular attention to the behaviour of intranodular contrast enhancement in dynamic phases.

The review process was independently performed by two operators (G.V. and M.A.) with 15 and 2 years of experience, respectively. In case of disagreement, the class indicated by the more experienced operator was assigned.

The reviewers were blinded to patient identity and final diagnosis. The specific targets of the review process were: (1) Nodule size; (2) the presence of APHE and the type of filling (global, rim, or peripheral discontinuous globular enhancement); and (3) the presence of washout during portal and parenchymal phases, focusing on its timing (before or after 60 s) and intensity (mild or marked); washout before 60 s was considered early, while washout happening after 60 s was considered late.

Inter-rater reliability of CEUS LI-RADS class assignment and of CEUS major features between the two raters (internal agreement) was evaluated for all the nodules (n = 511). Inter-rater reliability among our centre and two other operators from external centres (M.A.Z and G.I., both with more than 20 years of experience in CEUS) was also evaluated for a subgroup of 50 nodules (external agreement). To avoid an excess of typical HCCs, a total of 26 HCCs, 11 ICCs, 11 benign lesions, and 2 other malignancies were randomly selected for the external agreement analysis.

The entire process, including folder preparation, CEUS LI-RADS class assignment, and dataset preparation for analysis, was completed over a period of 5 mo. A systematic review of all CT and MRI scans was not performed.

Statistical analysis

Descriptive statistics (median, interquartile range, range, and percentage) were calculated for patients’ demographic and clinical characteristics (age, sex, aetiology of cirrhosis, number, and size of nodules). The normal distribution of continuous variables was evaluated through Shapiro-Wilk test. Discrete and qualitative variables are expressed as frequencies and percentages.

Sensitivity, specificity, positive predictive value (PPV), negative predictive value (NPV), diagnostic accuracy, Youden’s index, relative risk, odds ratio, positive likelihood ratio, and negative likelihood ratio were calculated to assess the accuracy of different CEUS-LR classes and subclasses in diagnosing HCC (LR-5, LR-4, and LR-4 and 5 merging class), ICC (LR-M), and malignancies (LR-3). The associations between different CEUS LI-RADS classes and definite diagnosis were evaluated by Pearson’s chi-square test or Fisher’s exact test. To determine the uncertainty of the estimates on sensitivity, specificity, PPV, NPV, and diagnostic accuracy, 95% confidence intervals (CIs) were calculated.

Cohen’s k and Fleiss’ k statistics were used to evaluate the interobserver agreement among different examiners in the assignment of the CEUS LI-RADS classes and identification of APHE (absent, homogeneous, or rim-like), and washout (absent, late and mild, or early and/or marked). Additionally, a visual graphical representation of the agreement was created, based on the agreement chart proposed by Bangdiwala[29]. All statistical tests were considered significant for a P value < 0.05. Data were analysed using Stata/MP version 17.0 (Statacorp LP, TX, United States) and R version 4.1.1 (The R Foundation for Statistical Computing, Vienna, Austria).

RESULTS

A total of 511 nodules identified in 269 patients were considered in this study. The complete dataset concerning patients and nodule characteristics is shown in Table 1.

Table 1 Characteristics of patients and hepatic nodules.

Item	Number or range
Nodules, n	511
Patients, n	269
Males, n (%)	219 (81.4)
Females, n (%)	50 (18.6)
Median age at first nodule (IQR; range)	69 years (61-75; 43-88)
Males (IQR; range)	67 years (59-74; 43-88)
Females (IQR; range)	74.5 years (71-78; 59-85)
Hepatic cirrhosis aetiology (n)
Chronic HCV infection, n (%)	129 (48)
Alcohol abuse, n (%)	45 (16.7)
Chronic HBV infection, n (%)	24 (8.9)
Chronic HCV infection + alcohol abuse, n (%)	21 (7.8)
Chronic HBV + HCV infection, n (%)	8 (3)
NASH, n (%)	6 (2.2)
ChronicHBV infection + alcohol abuse, n (%)	5 (1.9)
Other aetiologies, n (%)	6 (2.2)
Unknown aetiology, n (%)	25 (9.3)
Median diameter of nodules (IQR; range)	24 mm (16-36; 5-200)

IQR: Inter quartile range; HCV: Hepatitis C virus; HBV: Hepatitis B virus; NASH: Non-alcoholic steatohepatitis.

Four-hundred and fifty-two out of 511 nodules (88.5%) turned out to be malignant, consisting of 423 HCCs (82.8%), 23 ICCs (4.5%), 3 metastases (0.6%), and 3 other malignancies (0.6%). Non-invasive diagnosis was obtained for 409 nodules (80%), while histology was followed for 102 nodules (20%). Complete data concerning each definite diagnosis rate for every CEUS LI-RADS class are reported in Table 2. Table 3 shows the rates of HCC and ICC in different CEUS LI-RADS classes. The pathological findings for hepatic nodules are shown in Supplementary Table 1.

Table 2 Rates of different conclusive diagnoses for each Contrast-enhanced ultrasound Liver Imaging Reporting and Data System class.

		Conclusive diagnosis						%
		HCC	ICC	Metastasis	Other malignancy	Benign lesion	Total
CEUS LI-RADS class	CEUS LR-M	11	21	3	1	1	37	7.2
	CEUS LR-5	286	0	0	0	2	288	56.4
	CEUS LR-4	111	0	0	0	3	114	22.3
	CEUS LR-3	15	2	0	2	47	66	12.9
	CEUS LR-2	0	0	0	0	5	5	1.0
	CEUS LR-1	0	0	0	0	1	1	0.2
	Total	423	23	3	3	59	511	100.0
%		82.8	4.5	0.6	0.6	11.5	100.0

CEUS LI-RADS: Contrast-enhanced ultrasound Liver Imaging Reporting and Data System; HCC: Hepatocellular carcinoma; ICC: Intrahepatic cholangiocarcinoma.

Table 3 Rates of hepatocellular carcinoma and intrahepatic cholangiocarcinoma in different Contrast-enhanced ultrasound Liver Imaging Reporting and Data System classes.

CEUS LI-RADS class	HCC	ICC
LR-3	15/66 (22.7%)	2/66 (3%)
LR-4	111/114 (97.4%)	0/114 (0%)
LR-5	286/288 (99.3%)	0/288 (0%)
LR-M	11/37 (29.7%)	21/37 (56.8%)

CEUS LI-RADS: Contrast-enhanced ultrasound Liver Imaging Reporting and Data System; HCC: Hepatocellular carcinoma; ICC: Intrahepatic cholangiocarcinoma.

The most prevalent pattern in the arterial phase was homogeneous APHE (79.1% of all nodules), followed by isoenhancement (12.7%). In the portal and late phases, the majority of nodules showed a late and mild washout (60.7%) while the second most frequent pattern was isoenhancement (30.7%). See Table 4 and Table 5 for complete data on CEUS pattern in the arterial and venous phases, respectively.

Table 4 Rates of different contrast-enhanced ultrasound patterns in arterial phase.

Arterial phase CEUS pattern	Nodules, n (%)
Homogeneous hyperenhancement	404 (79.1)
Rim hyperenhancement	23 (4.5)
Globular hyperenhancement	1 (0.2)
Isoenhancement	65 (12.7)
Hypoenhancement	18 (3.5)

CEUS: Contrast-enhanced ultrasound.

Table 5 Rate of different portal and late phase contrast-enhanced ultrasound patterns.

Portal and late phase CEUS pattern	Nodules, n (%)
Late and mild washout	310 (60.7%)
Early/marked washout	27 (5.3%)
Isoenhancement	157 (30.7%)
Hypoenhancement	15 (2.9%)
Hyperenhancement	2 (0.4%)

CEUS: Contrast-enhanced ultrasound.

LR-M nodules

Thirty-seven lesions (7.2%) were assigned to the CEUS LR-M class (Figure 2A). Twenty-one of these nodules turned out to be ICCs, eleven were HCCs, three were metastases, one was a lymphoepithelioma, and one was benign. CEUS LR-M predicted ICC with a 91.3% sensitivity, 96.7% specificity, 56.8% PPV, 99.6% NPV, and 96.5% diagnostic accuracy (P < 0.001) (Table 6). Examining the CEUS behaviour of ICC, it was observed that 16 out of 21 nodules (76%) showed a rim APHE, while 11 out of 21 nodules (52%) showed an early washout (Supplementary Table 2). HCC nodules reported as LR-M showed a rim APHE in 6 out of 11 cases (54.5%) and an early washout in 7 out of 11 cases (63.6%; Supplementary Table 3).

Figure 2 Examples of different contrast-enhanced ultrasound Liver Imaging Reporting and Data System classes. A: Contrast-enhanced ultrasound (CEUS) LR-M. Notice rim arterial phase hyperenhancement and early washout, before 60 s; B: CEUS LR-5. Notice homogeneous arterial phase hyperenhancement, isoenhancement in portal phase, and mild washout in the late phase; C: CEUS LR-4. Notice homogeneous arterial phase hyperenhancement and isoenhancement in both portal and late phases; D: CEUS LR-3 iso-iso. Notice isoenhancement in all phases; E: CEUS LR-3 hypo-hypo. Notice hypoenhancement in all phases. The arrows show the target lesion.

Table 6 Diagnostic statistics of different contrast-enhanced ultrasound Liver Imaging Reporting and Data System classes for different diagnosis.

Tested association	Sensitivity (%)	Specificity (%)	PPV (%)	NPV (%)	Diagnostic accuracy (%)	Youden’s index	Odds Ratio	P value
CEUS LR M-ICC	91.3 (72.0-98.9)	96.7 (94.7-98.1)	56.8 (39.5-72.9)	99.6 (98.5-99.9)	96.5 (94.5-97.9)	0.880	309.75	< 0.001
CEUS LR 5-HCC	67.6 (62.9-72.1)	97.7 (92.0-99.7)	99.3 (97.5-99.9)	38.6 (32.1-45.3)	72.8 (68.7-76.6)	0.653	89.80	< 0.001
CEUS LR 4-HCC	26.2 (22.1-30.7)	96.6 (90.4-99.3)	97.4 (92.5-99.5)	21.4 (17.5-25.8)	38.4 (34.1-42.7)	0.228	10.10	< 0.001
CEUS LR 4/5-HCC	93.9 (91.1-95.9)	94.3 (87.2-98.1)	98.8 (97.1-99.6)	76.1 (67.0-83.8)	93.9 (91.5-95.8)	0.882	253.50	< 0.001
CEUS LR 3-benign lesion	79.7 (67.2-89.0)	95.8 (93.5-97.5)	71.2 (58.7-81.7)	97.3 (95.3-98.6)	93.9 (91.5-95.8)	0.755	89.26	< 0.001
CEUS LR-3-malignancy	4.2 (2.5-6.5)	20.3 (11.0-32.8)	28.8 (18.3-41.3)	2.7 (1.4-4.7)	6.0 (4.2-8.5)	-0.755	0.01	< 0.001
CEUS LR-3-iso-iso-malignancy	5.3 (0.1-26.0)	19.1 (9.1-33.3)	2.6 (0.1-13.5)	33.3 (16.5-54.0)	15.2 (7.5-26.1)	-0.756	0.01	< 0.001
CEUS LR-3-hypo-hypo-malignancy	57.9 (33.5-79.7)	91.5 (79.6-97.6)	73.3 (44.9-92.2)	84.3 (71.4-93.0)	81.8 (70.4-90.2)	0.494	14.78	< 0.001

CEUS: Contrast-enhanced ultrasound; HCC: Hepatocellular carcinoma; ICC: Intrahepatic cholangiocarcinoma; PPV: Positive predictive value; NPV: Negative predictive value.

LR-5 nodules

A total of 288 nodules (56.4%) were categorized as CEUS LR-5 (Figure 2B), of which 286 turned out to be HCC, and 2 were benign lesions. The median diameter of these nodules was 25 mm. The conclusive diagnosis was achieved by CT/MRI for 248 nodules and by histology for 40. CEUS LR-5 class predicted HCC with a 67.6% sensitivity, 97.7% specificity, 99.3% PPV, 38.6% NPV, and 72.8% diagnostic accuracy (P < 0.001) (Table 6).

LR-4 nodules

One-hundred and fourteen nodules (22.3%) were reported as CEUS LR-4 (Figure 2C), of which 111 were HCC and 3 were regenerative nodules, as confirmed by histology. The median diameter of these nodules was 21.5 mm. In 95 cases, the diagnosis was given by CT/MRI and in 19 cases by biopsy. CEUS LR-4 predicted HCC with a 26.2% sensitivity, 96.6% specificity, 97.4% PPV, 21.4% NPV, and 38.4% diagnostic accuracy (P < 0.001) (Table 6). Table 7 show data relative to different LR-4 patterns.

Table 7 Classification of nodules for LR-3, LR-4, and LR-5 classes, reported in yellow, orange, and red, respectively.

Nodule size	No APHE1		APHE1		Total
	< 20 mm	≥ 20 mm	< 10 mm	≥ 10 mm
No washout of any type	37 (4)	21 (5)	1 (1)	106 (104)	165
Late and mild washout	7 (5)	8 (7)	0	288 (286)	303
Total	44	29	1	394	468

¹With the exclusion of nodules with rim and peripheral discontinuous globular arterial phase hyper-enhancement belonging to contrast-enhanced ultrasound LR-M and contrast-enhanced ultrasound LR-1 classes, respectively.

Number of hepatocellular carcinomas in brackets. APHE: Arterial phase hyperenhancement.

LR 4-5 merged class

The merging of CEUS LR-4 and CEUS LR-5 classes predicted HCC with a 93.9% sensitivity, 94.3% specificity, 98.8% PPV, 76.1% NPV, and 93.9% diagnostic accuracy (P < 0.001) (Table 6).

LR-3 nodules

Sixty-six lesions (12.9%) were assigned to the CEUS LR-3 class (Figure 2D and E). Specifically, 15 of these nodules were HCCs, 2 were ICCs, 2 were other malignancies, and 47 were benign lesions. The median diameter of these nodules was 16 mm. Fifty-three lesions were diagnosed non-invasively by CT/MRI, while 13 by biopsy. CEUS LR-3 predicted benign lesions with a 79.7% sensitivity, 95.8% specificity, 71.2% PPV, 97.3% NPV, and 93.9% diagnostic accuracy (P < 0.001) (Table 6). Lesions belonging to the CEUS LR-3 class showed great heterogeneity. In fact, iso-iso nodules (Figure 2D) were most likely benign (only 1 malignancy out of 39 nodules), while other patterns showed a higher risk of cancer (18 malignancies out of 27). The second most frequent CEUS LR-3 pattern was the hypo-hypo pattern assigned to 15 nodules (Figure 2E), of which 11 were malignant (7 HCCs, 2 ICCs, 1 lymphoma, and 1 carcinosarcoma). The rate of malignancy for the CEUS LR-3 class and its subclasses are shown in Figure 3. We also calculated the correlation between specific CEUS LR-3 subgroups and malignancy, with analysis limited to CEUS LR-3 nodules (n = 66). It was observed that CEUS LR-3 iso-iso pattern predicted malignancy with a 5.3% sensitivity, 19.1% specificity, 2.6% PPV, 33.3% NPV, and 15.2% diagnostic accuracy (P < 0.001). Conversely, CEUS LR-3 hypo-hypo pattern predicted malignancy with a 57.9% sensitivity, 91.5% specificity, 73.3% PPV, 84.3% NPV, and 81.8% diagnostic accuracy (P < 0.001) (Table 6). Data concerning different LR-3 patterns are reported in Table 7.

Figure 3  Absolute frequency (n) of malignancies and benign lesions in LR-3 nodules and LR-3 subgroups with different contrast-enhanced ultrasound patterns.

LR 1-2 nodules

Only one nodule (0.2%) was categorized as CEUS LR-1, and five nodules (1%) as CEUS LR-2. All these nodules were found to be benign.

Interobserver agreement

The observed agreement between the two internal raters (1 and 2) for the assignment of CEUS LI-RADS class was 95.7%, with Cohen’s k = 0.94 (95%CI: 0.92-0.97, P < 0.0001), which represents an almost perfect agreement, according to Landis and Koch[30] classification. The agreement is clearly visualized in Figure 4A. Supplementary Table 4 shows the assignments of the two raters.

Figure 4 Bangdiwala’s agreement charts of the Contrast-enhanced ultrasound Liver Imaging Reporting and Data System class assignments between different raters. In the case of perfect agreement, the k rectangles are represented by perfect squares and the shaded squares determined by the diagonal cell entries are exactly equal to the rectangles; lesser agreement is visualized by comparing the area of the blackened squares to the area of the rectangles. A: Agreement chart between the two internal raters (1 and 2), with the exclusion of LR-1 and LR-2 classes due to their rarity (n = 505); B-D: Agreement charts among the three raters from different centres (2, 3, and 4) for the subgroup of 50 nodules. We list the agreement charts between raters 2 and 3 (B), between raters 2 and 4 (C), and between raters 3 and 4 (D).

The observed agreement among the three raters from different centres (2, 3, and 4) for the assignment of CEUS LI-RADS class was 68% and Fleiss’s k coefficient showed a value of 0.67 (P < 0.0001), which represents a substantial agreement. In particular, the agreement was almost perfect between raters 2 and 3 (k = 0.88, P < 1.7 × 10^-68), substantial between raters 2 and 4 (k = 0.66, P < 1.5 × 10^-14), and substantial between raters 3 and 4 (k = 0.61, P < 8.5 × 10^-10). The agreement is visualized in Figure 4B-D.

With regards to specific CEUS patterns, we found a higher degree of agreement for APHE (internal k = 0.86, P < 2.7 × 10^-214; external k = 0.8, P < 0.001) than for washout (internal k = 0.79, P < 1.6 × 10^-202; external k = 0.71, P < 0.001).

DISCUSSION

CEUS LI-RADS is a valuable diagnostic tool for non-invasive differential diagnosis of focal liver lesions in patients with cirrhosis. Based on our experience, employing this approach improves the performance of CEUS in the characterization of nodules, especially to discriminate between HCC and ICC.

In the current study, CEUS LR-5 was extremely specific for HCC with a very high PPV (99.3%). Only two false-positive results were observed, which were not ICC. We can therefore maintain that CEUS LR-5 is an appropriate tool for non-invasive diagnosis of HCC with virtually no risk of ICC misdiagnosis. Our data agree with recent publications on the subject[22]. However, CEUS LR-5 lacked sensitivity (67.6%) due to the large number of CEUS LR-4 nodules with a final diagnosis of HCC (97.4%). The high specificity of CEUS LR-5 for HCC combined with a low sensitivity was confirmed by a recent prospective multicentric study that compared the accuracy of different CEUS algorithms for the non-invasive diagnosis of HCC[31] and a recent meta-analysis[32].

Considering the high risk of HCC for the LR-4 class (97.4% PPV), the possibility of merging LR-4 and 5 classes was tested. By doing so, sensitivity in identifying HCC rose from 67.6% to 93.9%. The loss in specificity was low (from 97.7% to 94.3%), and was entirely attributed to two nodules > 10 mm classified as CEUS LR-4, which turned out to be benign. Data from the literature supports such an approach, showing that around 50% of HCCs do not display any washout in the portal and late venous phases on CEUS. In particular, Giorgio et al[33] demonstrated in their series that 55.4% of the biopsied HCC nodules < 20 mm showed this pattern after APHE. These findings were further corroborated by Leoni et al[34], who found that the hyper-iso pattern shows a high PPV (94%) for HCC and identifies nodules that are HCC or with a strong tendency to malignant progression. This pattern was detected in 36.2% (46 out 127) of HCCs[34].

Therefore, it should be considered that the introduction of the washout criteria in CEUS is based on findings from studies exploring the role of contrast-enhanced CT in the non-invasive diagnosis of HCC[35-37]. These findings were then extended to CEUS and MRI with little consideration for the differences in the pharmacokinetics of contrast agents among these techniques and the importance of the nodule visibility at baseline. Indeed, the requirement for washout as a diagnostic criterion is less stringent for CEUS and MRI, since these techniques have an improved capability to evaluate and determine whether APHE reflects the presence of a distinct nodule or merely abnormalities of intrahepatic vessels. CEUS, in particular, is performed for improved characterization of a nodule that has already been detected through conventional ultrasound.

Unfortunately, the introduction of washout in CEUS has significantly lowered the sensitivity of non-invasive diagnostic criteria for HCC. The inclusion of hyper-iso pattern among criteria for non-invasive HCC diagnosis might be a solution to increase CEUS sensitivity. Using this strategy, it can be concluded that there is no significant risk of overestimating the diagnosis of HCC, as in our series 98% of the nodules with the hyper-iso pattern were HCCs and only 2% were benign nodules. These considerations and results agree with another study on the combination of CEUS LR-4 and LR-5 criteria[38]. Furthermore, different studies demonstrated that the identification of washout has higher inter-rater variability than APHE identification[39,40]. These findings are also confirmed by the present study.

Regarding ICC, we observed that the majority of the nodules (21/23, 91.3%) were correctly diagnosed using the LR-M class of risk. Only two ICC cases were not assigned to this class due to a hypovascular aspect in all phases. The high sensitivity and specificity of the CEUS LR-M class for ICC (91.3% and 96.7%, respectively) in our series of patients demonstrate that this class is a valuable diagnostic tool for this type of cancer. Still, this class is not entirely specific for ICC as other types of malignancy can be found, such as HCC, metastatic lesions, and rarer malignancies[41]. We found that 11 out of 37 nodules (30%) classified as LR–M turned out to be HCC. This was due to the presence of an early washout (63.6% of nodules) and/or a rim enhancement pattern (54.5% of nodules). These observations are in agreement with the previously published literature. In particular, a multicentre retrospective study published by Terzi et al[22] reported that about 40% of LR-M lesions were HCCs. Another study by Wilson et al[16] identified that 35% of HCCs were reported to be LR-M. Several other authors have attempted to decrease the risk of HCC misdiagnosis by proposing a modified LR-M class of risk with the introduction of new criteria, such as the shortening of washout timing to < 45 s or the possibility to detect a significant washout to < 3 min[42-44]. Interestingly, Chen et al[45] were able to reduce the ICC misdiagnosis rate with CEUS LR-M from 38 to 12 cases by considering other criteria such as the presence of an intratumoral vein or an unclear boundary of the intratumoral non-enhanced area. However, we did not test these new criteria that require validation in multicentric and prospective studies. Another recent study by Huang et al[46] suggested that the integration of CEUS with the dosage of serum tumour markers (AFP and CA 19.9) improves the differentiation of LR-M nodules. Even though there are some limitations related to LR-M in this scenario, the adoption of this class of risk allows the improvement of diagnostic performance of CEUS for ICC, overcoming the drawbacks that resulted in the elimination of CEUS from the diagnostic flow charts of the most important hepatological international guidelines[3,8].

At present, CEUS LR-3 lesions are considered to hold an intermediate risk of malignancy, which is around 50% according to a recent study published by Terzi et al[22]. This rate was much lower in our case series (28.8%), which might be attributable to the lower figures of our study. Still, looking at the data from single centres in the multicentric study by Terzi et al[22], the rate of HCC in the CEUS LR-3 class ranged between 28.3% and 74.3%. One possible explanation for these results could be the high intrinsic heterogeneity of this class. Indeed, the algorithm only considers either the presence or absence of APHE, without any distinction between isoenhancement and hypoenhancement in all phases. However, in our clinical experience, hypo-hypo lesions are more likely to be malignant than iso-iso lesions. The present study confirmed this observation: Within the CEUS LR-3 class, the PPV for malignancy moved from 28.8% for CEUS LR-3 overall class to 2.6% for CEUS LR-3 iso-iso nodules, and 73.3% for CEUS LR-3 hypo-hypo nodules (Table 5). These considerations are in concordance with studies published before the advent of CEUS LI-RADS, when the problem of hypovascular nodules, which represent around 10% of HCC, was highlighted[47-49]. Likewise, we should be aware of the possibility of detecting ICC nodules in this class when a nodule shows hypoenhancement in all the phases; as observed in two out of 15 (13%) hypo-hypo nodules in our study. In light of these observations, we believe that it might be advantageous to split the CEUS LR-3 class into two subgroups (e.g., CEUS LR-3a and CEUS LR-3b) in order to separate iso-iso lesions from other patterns. To the best of our knowledge, this is the first study suggesting a CEUS LR-3 refinement based on real-life results. We believe that more attention should be directed towards the behaviour of nodule enhancement, rather than focusing on the size of the lesion alone.

Finally, this study demonstrated excellent inter-rater reliability of this classification system. Therefore, the use of CEUS LI-RADS in clinical practice could improve the reproducibility of CEUS and partially reduce the gap due to the difference in experience, as suggested by a recent study[50].

Our study also has some critical shortcomings, namely, its retrospective nature and the limited number of nodules analysed. These drawbacks are primarily due to the fact that data were collected from a single centre. Another debatable aspect of our investigation is the limited number of biopsies. However, we would like to highlight that current guidelines do not routinely recommend biopsy for nodules with typical HCC pattern on CT or MRI, allowing a non-invasive diagnosis[4,28].

Further prospective multicentric studies are warranted to confirm our findings and to investigate whether our considerations could be applied to the general population of patients with cirrhosis.

CONCLUSION

The present study supports the use of CEUS LI-RADS for the characterization of focal liver lesions in liver cirrhosis and the usefulness of LR-5 and LR-M classes to diagnose HCC and ICC, respectively. Additionally, our findings suggest that the merging of LR-4 and LR-5 classes provides innovative benefits in terms of diagnostic accuracy for HCC. Furthermore, it seems reasonable to split the CEUS LR-3 class into two subgroups to differentiate the risk of malignancy between iso-iso nodules, which are more likely to be benign, and other patterns, namely, hypo-hypo nodules, which are more likely to be malignant and not specific for HCC.

ARTICLE HIGHLIGHTS

Research background

Patients affected by liver cirrhosis are at high risk of developing hepatocellular carcinoma (HCC) and other malignancies such us intrahepatic cholangiocellular carcinoma (ICC). Diagnostic tools to characterize new-onset nodules in cirrhosis include contrast-enhanced ultrasound (CEUS), but this technique has been challenged for the possibility of misdiagnosing HCC and ICC.

Research motivation

The CEUS Liver Imaging Reporting and Data System (CEUS LI-RADS) aims to refine CEUS interpretation in order to improve the differentiation of HCC from other malignancies. Nevertheless, its effectiveness in real-life context has not yet been well established.

Research objectives

To test the accuracy of CEUS LI-RADS in correctly diagnosing HCC and ICC in cirrhosis with LR-5 and LR-M class, respectively, to evaluate the performance of LR-4 and 5 merging class in the diagnosis of HCC, and to investigate the rate of malignancies in different LR-3 patterns.

Research methods

This study consecutively collected 511 nodules in 269 cirrhotic patients from December 2008 to January 2020. A CEUS LI-RADS class was retrospectively attributed to each nodule based on review of CEUS examination. Common diagnostic accuracy indexes were assessed for the following associations: CEUS LR-5 and HCC; CEUS LR-4 and 5 merged class and HCC; CEUS LR-M and ICC; CEUS LR-3 and malignancy. The diagnostic standard was either biopsy or computed tomography/magnetic resonance imaging. The frequency of malignant lesions in CEUS LR-3 subgroups with different CEUS patterns was also determined.

Research results

CEUS LR-5 showed a 97.7% specificity for HCC with a low sensitivity (67.6%), while the CEUS LR-4 and 5 merged class showed a 93.9% sensitivity and 94.3% specificity for HCC. CEUS LR-M predicted ICC with a 91.3% sensitivity and 96.7% specificity. CEUS LR-3 predominantly included benign lesions (28.8% of malignancies) but was heterogeneous as the hypo-hypo pattern showed a higher rate of malignant lesions (73.3%) than the iso-iso pattern (2.6%).

Research conclusions

HCC diagnosis could benefit from the merging of CEUS LI-RADS classes 4 and 5. In addition, splitting LR-3 class could be advantageous to differentiate iso-iso nodules from other patterns with a higher risk of malignancy.

Research perspectives

Further prospective multicentric studies are necessary to confirm and extend our findings to the general population.

ACKNOWLEDGEMENTS

The authors thank Cabigiosu F for his help in data entry, and Fois SS for contributing to English language revision of the manuscript.