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Liver Resection and Simultaneous Sleeve Gastrectomy for MS-HCC (LIRESS)

Liver Resection and Simultaneous Sleeve Gastrectomy for HCC Related to Metabolic Syndrome (LIRESS)

Status
Not yet recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06060847
Acronym
LIRESS
Enrollment
50
Registered
2023-09-29
Start date
2024-03-06
Completion date
2032-03-06
Last updated
2023-12-19

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

Conditions

Carcinoma, Hepatocellular, Metabolic Syndrome

Keywords

hepatocellular carcinoma, sleeve gastrectomy, morbid obesity

Brief summary

Hepatocellular carcinoma (HCC) related to metabolic syndrome (MS) as unique risk factor is gradually overpassing the more common viral and alcohol etiology, becoming a global health issue. Liver surgery for metabolic syndrome-related HCC in this frail subset of patients constitute a challenge, due to high morbidity and mortality rate reported in literature, and contrasting results in term of oncologic outcome. The present multicentric prospective study aims to ascertain if the combination of sleeve gastrectomy and liver surgery in the same surgical procedure may have benefit in terms of reduced perioperative morbidity and prolonged Overall Survival and Recurrence Free Survival. Secondary outcome will be the evaluation of the consequences induced by sleeve gastrectomy on liver disease, in particular liver fibrosis evaluated in term of NFS score (Non-Alcoholic Fatty Liver Disease Fibrosis score), FIB-4 (Fibrosis-4 Index for Liver Fibrosis) score and Fibroscan transient elastography.

Detailed description

Obesity is a worldwide epidemic, with more than 2 billion people currently overweight and an additional 1.12 billion projected to be overweight by 2030. HCC (hepatocellular carcinoma) associated to obesity and its comorbidity is overcoming Hepatitis C Virus (HCV) related cancer and is already the leading cause of liver transplant in USA. HCC remains the sixth most common cancer in the world and the third cause of cancer-related death. Considering these epidemiological evidence, the incidence of MS-HCC (metabolic syndrome-related hepatocellular carcinoma) is expected to increase with huge cost efforts for the global healthcare system. The impaired performance status of patients with HCC and metabolic syndrome seems to explain high perioperative morbidity rate reported in literature. Literature reports several experiences of bariatric surgery combined to liver transplant for chronic liver disease related induced by non alcoholic steatohepatitis (NASH), performed before or after liver surgery, or even at the same time. Even if evidences are weak, outcomes reported seem to be promising. Since sleeve gastrectomy is not only a mere restrictive bariatric procedure, but it produces hormonal and metabolic changes, with the present study the investigators want to ascertain if sleeve gastrectomy at time of liver resection for MS-HCC (metabolic syndrome-related hepatocellular carcinoma) can modify short perioperative outcomes and long-term oncologic results.

Interventions

PROCEDURELiver resection and simultaneous sleeve gastrectomy for HCC induced by metabolic syndrome

Patients in the experimental arm will undergo liver resection for HCC and sleeve gastrectomy for MS during the same surgical procedure.

PROCEDURELiver resection for HCC induced by metabolic syndrome

Patients in the active comparator arm will undergo liver resection for HCC

Sponsors

Ospedale V. Fazzi
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Patients 18 years old and older, affected by hepatocellular carcinoma (HCC) with metabolic syndrome (MS) as unique risk factor, with compensated liver function (Child A) who are deemed suitable for liver resection and comply with the criteria for bariatric surgery, will undergo liver resection of HCC and simultaneous sleeve gastrectomy for morbid obesity during the same surgical procedure. Patients affected by HCC related to metabolic syndrome who fall within exclusion criteria, will undergo liver resection for HCC without sleeve gastrectomy.

Eligibility

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

Inclusion criteria

1. Be willing and able to provide written informed consent/assent for the trial 2. Be ≥ 18 years of age on day of signing informed consent. 3. Have hepatocellular carcinoma with metabolic syndrome as unique risk factor 4. Have an overall Child-Pugh score = A 5. Be eligible for liver resection with laparoscopic or robotic technique 6. Be eligible for bariatric surgery as defined below * BMI ≥ 40 kg/m2 * BMI ≥ 35-40 kg/m2 with associated comorbidities * BMI 30-35 kg/m2 and type 2 diabetes * BMI 30-35 kg/m2 and arterial hypertension with poor control despite optimal medical therapy.

Exclusion criteria

1. Have hepatocellular carcinoma related to other etiology, even in case of coexisting metabolic syndrome 2. Denial of the patient to undergo bariatric procedure 3. Have BMI \< 30 4. Have negative opinion of psychologic consultant 5. Have an overall Child-Pugh score \> 7 6. Evidence of clinical significant portal hypertension as followed: * esophageal varices * gastric varices * portal hypertensive gastropathy * gastric vascular ectasia Of note: 1) Conversion to open surgery for any reason does not represent a reason of data exclusion from the analysis; 2) any type of hepatic resection, according to Brisbane classification, is included, also major hepatectomy requiring preoperative intervention to achieve adequate volume remnant

Design outcomes

Primary

MeasureTime frameDescription
Overall Survival1 year, 3 years, 5 yearsCalculated from the date of diagnosis to the date of death from any cause
Recurrence-free Survival1 year, 3 years, 5 yearsCalculated from the date of surgery to the date of recurrence
90-day mortality90 post-operative daysMortality from any cause
Comprehensive Complication Index90 post-operative daysAny deviation from the normal postoperative course measured on a scale from 0 (no complication) to 100 (death)

Secondary

MeasureTime frameDescription
Weight lossAfter 3 months, up to 5 yearsWeight loss expressed in Kg
Percent excess weight lossAfter 3 months, up to 5 yearsPercent excess weight loss (%EWL) is calculated as follows: \[(initial weight - current weight) / (initial weight - ideal weight)\] × 100
Fibrosis-4 Index for Liver Fibrosis scoreAfter 6 months, up to 5 yearsFibrosis-4 Index for Liver Fibrosis score (FIB-4 score) will be calculated using the following formula: FIB-4 score= Age (years)× aspartate aminotransferase (AST) (U/L)/\[platelet count (109/L)×√alanine aminotransferase (ALT) (U/L)\]
Control of obesity-induced comorbiditiesAfter 3 months, up to 5 yearschange of insulin therapy or oral hypoglycemics assessed by medical history questionnaire
Control of obesity-induced hypertensionAfter 3 months, up to 5 yearsChange of antihypertensive therapy assessed by medical history questionnaire
Non-Alcoholic Fatty Liver Disease Fibrosis ScoreAfter 6 months, up to 5 yearsNon-Alcoholic Fatty Liver Disease Fibrosis Score (NFS score) will be calculated using the following formula: NFS = -1.675 + 0.037 - age (years) + 0.094 - BMI (kg/m2) + 1.13 × impaired fasting glucose/diabetes (yes = 1, no = 0) + 0.99 × aspartate aminotransferase/ alanine aminotransferase (AST/ALT) ratio - 0.013 × platelet count (×109/l) - 0.66 × albumin (g/dl).
Fibroscan stiffnessAfter 6 months, up to 5 yearsThe Fibroscan stiffness measurement relies on the propagation of elastic waves to assess the stiffness of the liver: the faster elastic waves propagates within the liver, the stiffer the organ is. The final liver stiffness value is the median of individual liver stiffness values using the valid measurements and is expressed in kilo Pascal (kPa).
Body Mass IndexAfter 3 months, up to 5 yearsBody Mass Index (BMI) is combination of bodyweight and body height and presented as kg/m\^2

Countries

Italy

Contacts

Primary ContactAnnarita Libia
libiamd@me.com0039 0833335284
Backup ContactAnnarita Libia
libiamd@me.com0039 0833335285

Outcome results

None listed

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