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

Sponsor
Ospedale V. Fazzi (Other)
Overall Status
Recruiting
CT.gov ID
NCT06060847
Collaborator
(none)
50
1
2
96
0.5

Study Details

Study Description

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.

Condition or Disease Intervention/Treatment Phase
  • Procedure: Liver resection and simultaneous sleeve gastrectomy for HCC induced by metabolic syndrome
  • Procedure: Liver resection for HCC induced by metabolic syndrome
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
50 participants
Allocation:
Non-Randomized
Intervention Model:
Parallel Assignment
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.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.
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Liver Resection and Simultaneous Sleeve Gastrectomy for HCC Related to Metabolic Syndrome (LIRESS)
Actual Study Start Date :
Sep 6, 2023
Anticipated Primary Completion Date :
Sep 6, 2028
Anticipated Study Completion Date :
Sep 6, 2031

Arms and Interventions

Arm Intervention/Treatment
Experimental: Patients affected by HCC induced by metabolic syndrome as unique risk factor

Patients aged 18 years old and older, affected by HCC with MS (metabolic syndrome) as unique risk factor who comply with the criteria for bariatric surgery, will undergo liver resection and sleeve gastrectomy with minimally-invasive technique in the same surgical procedure

Procedure: Liver 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.

Active Comparator: Patients with HCC related to metabolic syndrome as unique risk factor

Patients aged 18 years old and older, affected by HCC (hepatocellular carcinoma) with MS (metabolic syndrome) as unique risk factor who will undergo liver resection only

Procedure: Liver resection for HCC induced by metabolic syndrome
Patients in the active comparator arm will undergo liver resection for HCC

Outcome Measures

Primary Outcome Measures

  1. Overall Survival [1 year, 3 years, 5 years]

    Calculated from the date of diagnosis to the date of death from any cause

  2. Recurrence-free Survival [1 year, 3 years, 5 years]

    Calculated from the date of surgery to the date of recurrence

  3. 90-day mortality [90 post-operative days]

    Mortality from any cause

  4. Comprehensive Complication Index [90 post-operative days]

    Any deviation from the normal postoperative course measured on a scale from 0 (no complication) to 100 (death)

Secondary Outcome Measures

  1. Fibrosis-4 Index for Liver Fibrosis score [After 6 months, up to 5 years]

    Fibrosis-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)]

  2. Non-Alcoholic Fatty Liver Disease Fibrosis Score [After 6 months, up to 5 years]

    Non-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).

  3. Fibroscan stiffness [After 6 months, up to 5 years]

    The 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).

  4. Body Mass Index [After 3 months, up to 5 years]

    Body Mass Index (BMI) is combination of bodyweight and body height and presented as kg/m^2

  5. Weight loss [After 3 months, up to 5 years]

    Weight loss expressed in Kg

  6. Percent excess weight loss [After 3 months, up to 5 years]

    Percent excess weight loss (%EWL) is calculated as follows: [(initial weight - current weight) / (initial weight - ideal weight)] × 100

  7. Control of obesity-induced hypertension [After 3 months, up to 5 years]

    Change of antihypertensive therapy assessed by medical history questionnaire

  8. Control of obesity-induced comorbidities [After 3 months, up to 5 years]

    change of insulin therapy or oral hypoglycemics assessed by medical history questionnaire

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts 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

Contacts and Locations

Locations

Site City State Country Postal Code
1 Ospedale Vito Fazzi Lecce Italy 73100

Sponsors and Collaborators

  • Ospedale V. Fazzi

Investigators

  • Principal Investigator: Annarita Libia, Ospedale Vito Fazzi, Lecce

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Annarita Libia, Doctor, Ospedale V. Fazzi
ClinicalTrials.gov Identifier:
NCT06060847
Other Study ID Numbers:
  • 3/2023
First Posted:
Sep 29, 2023
Last Update Posted:
Sep 29, 2023
Last Verified:
Sep 1, 2023
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Annarita Libia, Doctor, Ospedale V. Fazzi
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 29, 2023