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HCC - Hepatocellular CarcinomaNCT07036874

Non-invasive Assessment for Outcome Prediction in Patients With Hepatocellular Carcinoma

An observational study of HCC - Hepatocellular Carcinoma and Cirrhosis, run by Chinese University of Hong Kong at 1 site in Hong Kong.

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Looking for participants now. Contact the study team or a site below to ask about taking part.

Sites and contacts
Official record

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Trial summary

This is a single-centre, prospective cohort study. Consecutive patients with compensated liver disease and hepatocellular carcinoma (HCC) for curative-intent treatment will be invited to this study. The study follow-up duration will be five years. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
HCC - Hepatocellular Carcinoma, Cirrhosis
What is being tested?
transient elastography and oesophagogastroduodenoscopy
How many people
159 participants
Where
1 siteHong Kong
Study dates
4 Nov 2024to Dec 2030
How long will I take part?
5 Years
Phase
Observational

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Study population: Consecutive adult patients with hepatocellular carcinoma fulfilling the inclusion and exclusion criteria will be invited to join the study.

Who may be able to join

  • Aged 18 or above
  • Known chronic liver disease(s)
  • HCC for curative-intent treatment (defined by HCC diagnosed with typical radiological features or histology, and planned for surgical resection or local ablative therapy as a curative-intent treatment)

Who cannot join

  • Current or history of decompensated liver cirrhosis (i.e. Child's C cirrhosis, prior decompensating events such as ascites, variceal bleeding, hepatic encephalopathy and hepatorenal syndrome)
  • o Child's B cirrhosis without decompensating events is not excluded
  • Past history of HCC (ie. The current HCC is a recurrence of priorly treated HCC or a second de novo HCC after previous first HCC)
  • Non-primary liver tumour (such as secondary liver tumour due to metastasis from another distant primary tumour)
  • History of liver transplantation or plan for liver transplantation as the modality of curative-intent HCC treatment
  • Asplenism or history of splenectomy
Show all 10Show fewer
  • Contraindication to OGD (eg. Intestinal perforation of obstruction)
  • Serious medical illness with limited life expectancy of less than 6 months
  • Pregnancy
  • Unable to obtain or refusal of informed consent from patient

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

Jimmy CT Lai, MB ChB contact

85235054205

jimmyctlai@cuhk.edu.hk

Angel Chim, MSc contact

angelchim@cuhk.edu.hk

Hong Kong1 site, 1 recruiting
  • Prince of Wales Hospital

    Hong Kong

    Jimmy CT Lai, MB ChB, 85235054205, jimmyctlai@cuhk.edu.hk

    Angel Chim, MSc, 85235054205, angelchim@cuhk.edu.hk

    Recruiting

Other trials in Hong Kong

About this study

Official title: Validation of Baveno VII Criteria and Spleen Stiffness Measurement on Outcome Prediction in Patients With Hepatocellular Carcinoma

This is a single-centre, prospective cohort study. Consecutive patients with compensated liver disease and hepatocellular carcinoma (HCC) for curative-intent treatment will be invited to this study. The study follow-up duration will be five years. The primary outcome is the composite of incident high-risk varices, hepatic decompensation and liver-related mortality. The participants will undergo transient elastography at baseline and then half-yearly post-HCC curative treatment; and oesophagogastroduodenoscopy (OGD) at baseline and then at year 1, 3 and 5 post-HCC curative treatment. Clinical assessments and laboratory tests will also be done at baseline and every 6 months until year 5 to identify any clinical events.

Read the detailed description

1.1 Significance of chronic liver disease and hepatocellular carcinoma

Hepatocellular carcinoma (HCC) burdens the global healthcare system with a drastic increase in incidence by 70% from 1990 to approximately 747,000 cases and 480,000 deaths in 2019.

Despite implementation of screening ultrasound in at-risk populations and advances in the treatment of HCC in recent decades, HCC remains a lethal malignancy with a median survival of less than a year. Apart from the oncological factors, the underlying liver disease has an important impact on morbidity and mortality in patients with HCC as most HCC develop under the setting of chronic hepatic inflammation and fibrosis from patients with advanced chronic liver diseases of various aetiologies.

1.2 Non-invasive measurement of portal hypertension

In the Baveno VI consensus, the term "compensated advanced chronic liver disease" (cACLD) described spectrum of chronic liver diseases ranging from advanced liver fibrosis to compensated cirrhosis. Patients with cACLD are at risk of hepatic decompensation and development of HCC, especially for those with clinically significant portal hypertension (CSPH), which is conventionally measured invasively by hepatic venous pressure gradient (HVPG). The recently updated Baveno VII consensus implemented a non-invasive approach by incorporating liver stiffness measurement (LSM) by vibration-controlled transient elastography (VCTE) and platelet count in ruling in or out CSPH in patients with cACLD. In the Baveno VII consensus and as well incorporated into the latest practice guidance on portal hypertension, LSM ≤ 15kPa and platelet count ≥ 150 x 109/L rules out CSPH, whereas LSM > 25kPa, LSM 20-25kPa with platelet count <150 x 109/L or LSM 15-20kPa with platelet count <110 x 109/L rule in CSPH, prompting the presence of gastroesophageal varices. As well in Baveno VI consensus, LSM < 20 kPa with platelet count > 150 x 109/L also implies a minimal risk of high-risk varices and thus can have a screening oesophagogastroduodenoscopy (OGD) spared.

The development of spleen stiffness measurement (SSM) by VCTE also revolutionised the field by demonstrating its correlation with portal pressure and CSPH. Studies have shown that, by combining Baveno VII criteria with SSM, the accuracy in identifying CSPH (such as the presence of high-risk varices) was enhanced compared to adopting Baveno VII criteria alone.

1.3 Unmet need 1: Conflicting data on LSM/SSM in prediction of hepatic events in HCC patients

Use of LSM and SSM in prediction of HCC recurrence was reported in a few previous studies. The studies involved a one-stop LSM and/or SSM measurements with longitudinal follow-up on the recurrence rate of HCC. For instance, high baseline LSM was shown to be a poor prognostic factor in patients with HCC receiving radiofrequency ablation, and achieving low LSM reduced HCC recurrence. Another prospective study involving 175 patients with HCC suitable for resection showed that SSM was the only predictor for late HCC recurrence.

However, there are lack of data in the prediction of hepatic decompensation in patients with HCC. First, studies aiming to investigation on risk prediction of decompensation either excluded patients with HCC or regarded HCC as one of the study endpoints. Second, the present data available also showed conflicting results. For instance, two retrospective studies performed from our group suggested that Baveno VII criteria (i.e. LSM by VCTE and platelet count) could accurately identify high risk varices and hepatic events in both advanced HCC and that of different Barcelona Clinic Liver Cancer (BCLC) stages. On the contrary, another retrospective suggested that the use of both Baveno VI or VII criteria were inaccurate in predicting the presence of high-risk varices or CSPH measured by HVPG across different stages of HCC. Heterogeneity was present in the study subjects and data analysis among different studies, leading to divergent results. SSM as well was not included in these studies and that the effect of combined Baveno VII and SSM in prediction of decompensation in HCC patients is still uncertain.

Being tested
transient elastography and oesophagogastroduodenoscopy
Keywords
hepatocellular carcinoma, liver stiffness, spleen stiffness
Medical subject headings
Carcinoma, Hepatocellular, Fibrosis

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • transient elastography and oesophagogastroduodenoscopyDiagnostic test

    Liver and spleen stiffness will be measured by transient elastography. Varices will be identified by oesophagogastroduodenoscopy.

Study groups in NCT07036874
Study groupRoleWhat they receive
Patients with hepatocellular carcinomaAdult patients with known chronic liver disease and hepatocellular carcinoma planning for curative-intent treatment
Receives: Diagnostic Test: transient elastography and oesophagogastroduodenoscopy

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Composite of incident high-risk varices, hepatic decompensation and liver-related mortality

    Composite of incident high-risk varices, hepatic decompensation and liver-related mortality

    Measured: 5 years

Secondary outcomes (4)
  1. Development of each hepatic decompensation event

    Development of each hepatic decompensation event

    Measured: 5 years

  2. Recurrence of hepatocellular carcinoma

    Recurrence of hepatocellular carcinoma

    Measured: 5 years

  3. Changes in Child-Pugh and Model for End-stage Liver Disease scores

    The minimum and maximum Child-Pugh score are 5 and 15, respectively. The minimum and maximum Model for End-stage Liver Disease score are 6 and 40, respectively. A higher score denotes worse outcome in both score.

    Measured: 5 years

  4. Change in liver and spleen stiffness measurements

    Change in LSM and SSM

    Measured: 5 years

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted25 Jun 2025
  2. Study start4 Nov 2024
  3. Primary completionDec 2030 (estimated)
  4. Study completionDec 2030 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
159 participants (estimated)
Target duration
5 Years
IDs, dates and publications
ClinicalTrials.gov ID
NCT07036874
Sponsor's protocol ID
2024.249
Status last verified
Oct 2026
First submitted
17 Jun 2025
Last updated
20 Oct 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Yes: Data may be shared upon reasonable request.

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