Liver Metastasis Colon Cancer
Conditions
Keywords
Liver, Interventional radiology, Portal vein embolization, Portal and hepatic vein embolization, Future liver remnant, Surgery, Non-cirrhotic liver, Liver metastases, Colorectal cancer, Liver Regeneration, Liver resection
Brief summary
The hypothesis is that liver venous deprivation (LVD) could strongly improve hypertrophy of the future remnant liver (FRL) at 3 weeks, as compared to portal vein embolization (PVE) in patient with liver metastases from colo-rectal origin considered as resectable.
Detailed description
Portal vein embolization (PVE) has been widely used to generate hypertrophy of the nonembolized lobe in patients undergoing major hepatectomy in order to prevent small-for-size remnant liver resulting in post-operative liver insufficiency. Although PVE is a safe and effective procedure, it does not always induce sufficient hypertrophy of the future remnant liver (FRL) even after a long time. In case of insufficient liver regeneration following PVE, some authors suggested to embolize hepatic vein(s) (Hwang, Ann Surg 2009). Interestingly, the sequential right hepatic vein embolization (HVE) after right PVE demonstrated an incremental effect on the FRL. Although attractive, this approach requires two different procedures and does not spare time as compared to PVE alone. To shorten and optimize the phase of liver preparation before surgery,the so-called liver venous deprivation (LVD) technique that combines both PVE and HVE during the same procedure was developed. The aim of this randomized phase II trial is to compare the percentage of change in FRL volume at 3 weeks after LVD or PVE using MRI or CT-scan.
Interventions
PROCEDURELiver preparation before major hepatectomy
Simultaneous portal and hepatic vein embolization versus Portal vein embolization, also called venous deprivation OR portal vein embolization.
Sponsors
Federation Francophone de Cancerologie Digestive
University Hospital, Montpellier
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Liver metastases from colo-rectal origin considered as resectable (as validated by a multidisciplinary committee with at least one senior hepatic surgeon) provided sufficient FRL volume * Percentage of FRL volume \< 30% * Age ≥ 18 years * General health status World Health Organisation 0,1 * Estimated life expectancy \> 3 months * Patients whose biological parameters are : * Platelets ≥100,000/mm3, * Polynuclear neutrophils ≥ 1000/mm3, * Hemoglobin≥ 9g/dL (even transfused patients can be included) * Creatininemia \< 1.5 times the normal value * Creatinine clearance \> 30 milliliters (mL)/min * Bilirubinemia ≤ 1,5 times the normal value * liver transaminases ≤ 5 times the normal value * prothrombin rate \> 70% * Reference liver CT-Scan or MRI done during the 30 days preceding PVE or LVD. * Written informed consent * National health insurance cover
Exclusion criteria
* Patient with cirrhosis * Presence of clinical ascites * Ongoing participation or participation within the 21 days prior to inclusion in the study in another therapeutic trial with an experimental drug * Serious non-stabilized disease, active uncontrolled infection or other serious underlying disorder likely to prevent the patient from receiving the treatment * Pregnancy (betaHCG positive), breast-feeding or the absence of effective contraception for women of child-bearing age * Contraindication for the MRI : Pacemaker or neurosensorial stimulator or implantable defibrillator, cochlear implant, ferromagnetic foreign body similar to the nervous structure. * Allergy or contra-indication to iodine contrast agents (thyrotoxicosis, allergy to the active substance or excipients) * Treatment with anticoagulants (heparin or AVK) that cannot be interrupted for 48 hours * Treatment with anti-platelets that cannot be interrupted for 5 days for aspirin or Plavix * Legal incapacity (persons in custody or under guardianship) * Deprived of liberty Subject (by judicial or administrative decision) * Impossibility to sign the informed consent document or to adhere to the medical follow-up of the trial for geographical, social or psychological reasons
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| increase in volume of the future remnant liver (FRL) | at 3 weeks after liver venous deprivation (LVD) or portal vein embolization (PVE) using MRI or CT-scan | The primary outcomes is to compare the increase in volume of the future remnant liver (FRL) |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Post-operative mortality | 90 days after surgery | Post-operative mortality defined as any death within 90 days after surgery or within the hospital stay |
| Post-operative morbidity | 90 days after surgery | Post-operative morbidity defined as the percentages of grade I/II/III/IV/V complications according to Clavien-Dindo classification within the 90 days after surgery or within the hospital stay. |
| Post-hepatectomy liver failure | between the day of the surgery and 90 days after surgery | Post-hepatectomy liver failure defined according to the 50-50 criteria or peak bilirubin \>7mg/dL. |
| Rate of non-resectability due to insufficient FRL | between the day of the treatment and the day of the surgery | Rate of non-resectability due to insufficient FRL defined as the percentage of patients for whom resection will be not attempted due to insufficient FRL |
| Rate of non-resectability due to tumor progression | between the day of the treatment and the day of the surgery | Rate of non-resectability due to tumor progression defined as the percentage of patients for whom resection will not be attempted due to tumor progression. |
| Rate of per-operative difficulties | between the day of the surgery and 90 days after surgery | Rate of per-operative difficulties defined as the percentage of patients for whom per-operative difficulties are encountered by the surgeon |
| Blood loos, operating time, transfusion | the day of the surgery | Blood loss are evaluated in mL. Operating time avec evaluated in minutes and transfusion are evaluated by number of packed red blood cells |
| Tolerance | between the day of liver preparation and 90 days after surgery | Toxicities are evaluated according to NCI-CTCAE version 4.03 published 14 June 2010 |
| R1 resection rate | the day of the surgery | Rate of R1 resection defined as the percentage of patients resected with margin \<1mm |
| Pre and post-operative liver volumes | Baseline, week 1, week 3 then every 2 weeks until surgery or week 7 and 4 weeks after surgery | Pre and post-operative liver volumes will be evaluated through CT or MRI acquisitions by calculating whole liver, tumor and FRL volumes |
| Recurrence-free survival | 90 days after surgery | Recurrence-free survival defined as the time from date of randomization to date of recurrence or death from their tumor. Patients alive will be censored at the date of last news. |
| Overall survival | Between the liver preparation and 90 days after surgery | Overall survival defined as the time from date of randomization to date of death from any cause. Patients alive will be censored at the date of last news. |
| Evaluation of pre and post-operative liver function | Baseline, week 1, week 3 then every 2 weeks until surgery or week 7 and 4 weeks after surgery | Evaluation of pre and post-operative liver function will be evaluated using 99mTc mebrofenine scintigraphy through SPECT/CT acquisitions by calculating mebrofenin clearance in %/min/m² of whole liver and FRL at the same time points as CT/MRI |
| To search for biomarkers predictive of liver hypertrophy/regeneration and immune cell response | The day of liver preparation, on day 1, day 2 and day 3 after liver preparation and the day of surgery | Biomarkers predictive of liver hypertrophy/regeneration are evaluated by blood samples and liver biopies |
| R0 resection rate | the day of the surgery | Rate of R0 resection defined as no microscopic tumor residual |
Countries
France
Outcome results
None listed