Comparison of Hypothermic Versus Normothermic Ex-vivo Preservation.

End Stage Liver DIsease Clinical Trial

— DCDNet  

Official title:

Optimization of an Evidence-based Organizational Model of Liver and Pancreas Transplant Using Cardiac Death Donors: a Pilot, Prospective, Randomized, Multicenter Study for the Comparison of Hypothermic Versus Normothermic Ex-vivo Preservation.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04744389
• Other study ID #: D52F20000740002
• Status: Recruiting
• Phase: N/A
• Start date: December 15, 2020
• Est. completion date: March 31, 2023

Study information

• Verified date: July 2022
• Source: Azienda Ospedaliero, Universitaria Pisana
• Contact: Davide Ghinolfi, MD, PhD
• Phone: 00393282185278
• Email: d.ghinolfi[@]ao-pisa.toscana.it
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Study groups: The study is a multicenter (Pisa and Milan), prospective, randomized study comparing D-HOPE (HMP) vs NMP in DCD and ECD-DBD (extended criteria brain-dead donors). Once a DCD or a DBD with extended criteria (ECD-DBD) meets the inclusion criteria, they are randomized as follow: 1. 20 liver grafts from DCD after normothermic regional perfusion (NRP) matching the inclusion criteria are randomized 1:1 to hypothermic machine perfusion (HMP) vs normothermic machine perfusion (NMP) and then transplanted. 2. 40 liver grafts from ECD-DBD matching the inclusion criteria are randomized 1:1 to hypothermic machine perfusion (HMP) vs normothermic machine perfusion (NMP) and then transplanted

Description:

The persistent mismatch between patients waiting for a liver transplant (LT) and grafts availability promoted the use of donation after circulatory death (DCD). Italian law requires 20 minutes of continous flatline electrocardiogram to declared individual's circulatory death and such a long period of warm ischemia time forced the development of protocols using abdominal normothermic regional perfusion (NRP) followed by ex-vivo graft reperfusion by means of machine perfusion technology (MP) for its potential to minimize ischemia/reperfusion damage and promote organ repair and reconditioning prior to transplantation. An extensive evaluation of all DCD donors might increase donation rate by 30%, but, while kidney transplant from DCD donors is well implemented, no definitive data exist on the optimal use of NRP and MP in liver and pancreas transplantation and an organizational model is far to be implemented. Moreover, a randomized trial comparing hypothermic vs normothermic ex-vivo perfusion has never been performed. The proposed project will perform a pilot, open, randomized, prospective trials to evaluate the sequential use of NRP followed by ex-vivo MP (hypothermic (HMP) vs normothermic (NMP)) by measuring several indicators of organ damage and recovery with the target to set up the optimal organizational model for DCD donation: 1. Twenty LT from DCD donors after NRP (considered transplantable for the acceptance criteria in use) will be randomized 1:1 to ex-vivo HMP or NMP (multicenter study together with the center in Milan) 2. 40 liver grafts from ECD-DBD matching the inclusion criteria are randomized 1:1 to hypothermic machine perfusion (HMP) vs normothermic machine perfusion (NMP) and then transplanted To assess organ damage and repair capacity, the following investigations will be performed: -biomarkers of apoptosis, necrosis, innate-mediated inflammation and its resolution, angiogenesis and thrombosis during NRP -circulating biomarkers indicating damage, proliferation, angiogenetic and tissue remodelling factors; a targeted-metabolomic and lipidomic profiling during ex-vivo HMP or NMP in the perfusate and on blood samples in the peri and post-operative period; bile composition on graft subjected to NMP. Evaluation of necrosis, apoptosis and proliferation, immunohistochemical analysis, a targeted-metabolomic and lipidomic profiling, ATP measurement, and electronic microscopy investigations will be performed on liver tissue and bile duct biopsies after NRP, before and after ex-vivo reperfusion, and immediately after reperfusion in the recipient (only for transplantable grafts) Based on the collected data a new algorithm of organ evaluation, procurement, preservation and reconditioning will be formulated and disseminated.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 60
• Est. completion date: March 31, 2023
• Est. primary completion date: September 30, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years to 75 Years

Eligibility

GRAFT:

Inclusion criteria:

DCD:

• no absolute contraindications as per Italian National Transplant center (CNT)
• donor age =70 years
• witnessed and documented cardiac arrest
• macro-vescicular steatosis <30% at liver biopsy
• necrosis <5% at liver biopsy
• fibrosis <2 as per Ishak's score at liver biopsy
• arteriolar thickening <60% at liver biopsy
• WIT =160 minutes
• ALT <1000 UI/L during NRP
• downward trend lactate during NRP

DBD:

• no absolute contraindications as per Italian National Transplant center (CNT)
• donor age > 70 years
• macro-steatosis between 30 and 50% at liver biopsy Exclusion criteria:

DCD:

• absolute contraindications as per Italian National Transplant center (CNT)
• donor age >70 years
• macro-vescicular steatosis >30% at liver biopsy
• necrosis >5% at liver biopsy
• fibrosis >2 as per Ishak's score at liver biopsy
• severe macroangiopathy (arteriolar thickening >60% at liver biopsy)
• WIT >160 minutes
• ALT >1000 UI/L during NRP
• uptrend lactate during NRP

DBD:

• absolute contraindications as per Italian National Transplant center (CNT)
• donor age < 70 years
• macro-steatosis between > 50% at liver biopsy RECIPIENTS

Inclusion criteria:

• Subject must be greater than or equal to 18 years of age.
• Subject with end-stage liver disease who is actively listed for primary liver transplantation
• Subject, or a legally authorized representative, has given informed consent to participate in the study

Exclusion criteria:

• Subject is currently listed as a UNOS status 1A.
• Subject is requiring oxygen therapy via ventilator/respiratory support.
• Subject is planned to undergo simultaneous solid organ transplant.
• Subject is pregnant at the time of transplant.
• Subject MELD score 25 or higher
• Subject receives re-transplantation of liver.
• Any medical conditions contro-indicating the use of DCD grafts at transplant surgeon/hepatologist evaluation

Related Conditions & MeSH terms

• End Stage Liver DIsease
• Hypothermia
• Liver Diseases

Intervention

Device:
• Hypothermic Machine Perfusion
The perfusion system was primed with 4 L of Belzer machine perfusion solution University of Wisconsin Machine Perfusion Solution (Bridge for Life, Ltd., Columbia, SC). The arterial and portal pressures were set at 25 mm Hg with a flow and at 3-4 mm Hg with a continuous flow, respectively. The oxygen flow was set at 0.25 L/minute. The target liver temperature was between 4°C and 10°C.
• Normothermic Machine Perfusion
Grafts were perfused at 37°C in an OR next to the transplant OR and under medical supervision using a blood-based perfusate. Initial perfusate temperature was set at 20°C and raised by 1°C every 2 minutes. Oxygenation was provided by an anesthesia ventilator initially set at 4 L/minute with 30% fraction of inspired oxygen, and later adjusted based on perfusate pH, partial pressure of oxygen, and partial pressure of carbon dioxide. Blood gas analyses were drawn every 20 minutes during the first hour and every 30 minutes thereafter with the aim to maintain a physiological pH and ionogram result, and a partial pressure of oxygen between 200 and 250 mm Hg. Perfusate glucose, transaminases, and lactate were measured during NMP as were bile production and quality (pH, sodium, glycemia, lactate, and HCO3)

Locations

Country	Name	City	State
Italy	UO Chirurgia Epatica e del Trapianto di Fegato	Pisa

Sponsors (3)

Lead Sponsor	Collaborator
Azienda Ospedaliero, Universitaria Pisana	Fondazione C.N.R./Regione Toscana "G. Monasterio", Pisa, Italy, Fondazione IRCCS Ca' Granda, Ospedale Maggiore Policlinico

Country where clinical trial is conducted

Italy, 

References & Publications (2)

Ghinolfi D, Dondossola D, Rreka E, Lonati C, Pezzati D, Cacciatoinsilla A, Kersik A, Lazzeri C, Zanella A, Peris A, Maggioni M, Biancofiore G, Reggiani P, Morganti R, De Simone P, Rossi G. Sequential Use of Normothermic Regional and Ex Situ Machine Perfusion in Donation After Circulatory Death Liver Transplant. Liver Transpl. 2021 Feb;27(3):385-402. doi: 10.1002/lt.25899. Epub 2020 Nov 8. — View Citation

Ghinolfi D, Rreka E, De Tata V, Franzini M, Pezzati D, Fierabracci V, Masini M, Cacciatoinsilla A, Bindi ML, Marselli L, Mazzotti V, Morganti R, Marchetti P, Biancofiore G, Campani D, Paolicchi A, De Simone P. Pilot, Open, Randomized, Prospective Trial for Normothermic Machine Perfusion Evaluation in Liver Transplantation From Older Donors. Liver Transpl. 2019 Mar;25(3):436-449. doi: 10.1002/lt.25362. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Rate of graft loss	Death of patient, relisting or Retransplantation. Composite Outcome	at 6 months postoperatively
Primary	Rate of Ischemic Type Biliary Lesions (ITBL)	ITBL as assessed by MRI / MRCP. Composite Outcome	at 6 months postoperatively
Secondary	1-year graft survival		1-year postoperatively
Secondary	1-year patients survival		1-year postoperatively
Secondary	level of BCL-2/BAX at the liver histology	BCL-2/BAX is members of the Bcl-2 family of regulator proteins that regulate cell death and correlates with graft loss	after 2 hours of perfusion
Secondary	level of Soluble Keratin 18 in the perfusate	Soluble Keratin 18 is a marker of necrosis and apoptosis and correlates with graft loss	after 2 hours of perfusion
Secondary	level of HMGB1in the perfusate	HMGB1 Acts as danger associated molecular pattern (DAMP) molecule that amplifies immune responses during tissue injury and correlates with graft loss	after 2 hours of perfusion