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Prognostic Factors for HCC and Liver Transplantation in Patients With MASLD/MASH

Prognostic Factors for the Development of Hepatocellular Carcinoma (HCC) and Indications for Liver Transplantation in Patients With Metabolic Liver Diseases (MASLD/MASH): The BOMASH Study

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06813508
Acronym
BOMASH
Enrollment
1000
Registered
2025-02-07
Start date
2024-11-20
Completion date
2044-11-20
Last updated
2025-02-07

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hepatocellular Carcinoma, Liver Transplant, Metabolic Dysfunction-Associated Steatohepatitis, Metabolic Dysfunction-Associated Steatotic Liver Disease

Brief summary

The BOMASH study is a single-center, prospective/retrospective observational study without pharmacological interventions. It will include all patients diagnosed with Metabolic-Associated Steatotic Liver Disease (MASLD/MASH), whether newly diagnosed or previously identified at the center during follow-up or as part of routine diagnostic and therapeutic care. The aim of the study is to identify predictive factors related to the prognosis of patients with metabolic liver disease (MASLD/MASH). Specifically, the study seeks to uncover biomarkers that can identify individuals at risk of requiring a liver transplant or developing HCC.

Detailed description

The BOMASH study is a single-center, prospective/retrospective observational study without pharmacological interventions. It will include all patients diagnosed with Metabolic-Associated Steatotic Liver Disease and Metabolic-Associated Steatohepatitis (MASLD/MASH), whether newly diagnosed or previously identified at the center during follow-ups or as part of routine diagnostic and therapeutic care. MASLD is characterized by significant variability in terms of severity and progression rates. Although a large portion of the population is at risk, only a minority develop liver-related comorbidities. Epidemiological studies reveal that patients with MASH have a higher risk of developing liver-related complications compared to those with simple steatosis (MASLD). However, the factors driving progression to MASH and its advanced stages remain unclear, and disease staging can only be accurately determined through liver biopsy. Given the large number of individuals at risk for MASLD, liver biopsy is not a feasible screening tool for widespread use. Key challenges involve understanding the biological and environmental factors that drive variability among MASLD patients and using this knowledge to develop effective methods for risk stratification, enabling targeted treatment for individuals at the highest risk. The identification of risk factors through the combination of non-invasive tests (serum biomarkers and non-invasive techniques) can enable risk stratification for hepatocellular carcinoma (HCC) development and identify individuals who may require liver transplantation. A study on MASLD represents a valuable tool to enhance understanding of this nosological entity and to support basic, clinical, and epidemiological research. It also benefits individuals affected by these conditions and assists national and local authorities in planning and optimizing healthcare and social services. Systematic data collection on MASLD can be instrumental in identifying previously unrecognized risk factors that may predispose individuals to more aggressive and treatment-resistant forms of the disease. Analyzing the collected data could highlight potential common markers among patients whose MASLD diagnosis progresses to HCC and subsequently necessitates liver transplantation. These findings would provide useful prognostic factors for patient management. In conclusion, the opportunity to longitudinally track disease progression in a large cohort of patients with chronic metabolic liver disease could pave the way for strategies that make the management of this highly prevalent condition more sustainable for national and regional healthcare systems. Therefore, the aim of the study is to identify predictive factors related to the prognosis of patients with metabolic liver disease (MASLD/MASH). Specifically, the study seeks to uncover biomarkers that can identify individuals at risk of requiring a liver transplant or developing HCC.

Interventions

None listed

Sponsors

IRCCS Azienda Ospedaliero-Universitaria di Bologna
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
OTHER

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* All patients with a diagnosis of MASLD, established according to the most recent published guidelines (EASL, EASD, EASO) * Age ≥18 years Inclusion Criteria for Biological Sample Collection: * Patients requiring liver biopsy for diagnostic purposes, as indicated by the most recent published guidelines (EASL, EASD, EASO)

Exclusion criteria

* No

Design outcomes

Primary

MeasureTime frameDescription
Number of hepatocellular carcinoma (HCC) or liver transplantation (OLT) cases and time to onset.From enrollment to november 2044The aim of the study is to identify predictive factors related to the prognosis of patients with liver disease of dysmetabolic origin: Metabolic-Associated Steatotic Liver Disease and Metabolic-Associated Steatohepatitis (MASLD/MASH). Specifically, the aim is to identify markers that can predict individuals who will later require a liver transplant or develop hepatocellular carcinoma.

Secondary

MeasureTime frameDescription
Response rate in patientsFrom enrollment to november 2044Objective response rate in patients with HCC or those requiring liver transplantation, measured using RECIST 1.1 criteria.
Number of cases of liver complicationsFrom enrollment to november 2044Cases of liver decompensation, major adverse cardiovascular events (MACE), extrahepatic tumors, and liver transplantation, along with their time of onset.
Response to dietologic and pharmacological therapies related to glycated hemoglobin levelsFrom enrollment to november 2044Positive response to dietetic and drug therapies is measured by glycated hemoglobin levels.
Incidence of HCC and liver transplantation (OLT)From enrollment to november 2044Calculate the incidence of liver transplantation and the occurrence of HCC for this disease.
Response to dieto-therapeutic and pharmacological therapies related to biochemical parametersFrom enrollment to november 2044Positive response to dietetic and pharmacological therapies is measured by biochemical parameters (Aspartate amino transferase, Alanina amino transferase).
Number of HCC or liver transplantation (OLT) cases categorized by MASLD and MASHFrom enrollment to november 2044
Response to dieto-therapeutic and pharmacological therapies related to weightFrom enrollment to november 2044Positive response to dietetic and pharmacological therapies is measured by weight loss.

Countries

Italy

Contacts

Primary ContactFabio Piscaglia, MD
fabio.piscaglia@unibo.it+39 051 2142542
Backup ContactFederico Ravaioli, MD PhD
f.ravaioli@unibo.it+39 0512142717

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026