Search for Transcriptional Biomarkers in a Conversion Protocol From Calcineurin Inhibitors to Mycophenolate Mofetil

NCT ID: NCT01321112

Last Updated: 2012-05-10

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: NA
• Total Enrollment: 40 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2011-02-28
• Study Completion Date: 2014-03-31

Brief Summary

As is well known, immunosuppressive treatment (IS) after liver transplantation has several and frequents adverse effects that limit the survival of the graft and recipients. Because of that, it is desirable that these recipients were able to receive a mild IS regime with a better safety profile. An attempt to get that aim has been evaluated in several trials in the past, and consist in to change the IS regime from an calcineurin inhibitors (CNI) based to another less intense and with less adverse effects based on mycophenolate mofetil (MMF), which is known to have a better safety profile. The success rate of this strategy(i.e. complete conversion in absence of rejection) has a wide range from 100% to 50% approximately. However it is accepted that this strategy is associated with the improvement of several adverse effects of CNIs such as renal failure and dyslipemia. This study's aim is to perform IS conversion from CNI to MMF monotherapy and look for transcriptional biomarkers employing a whole genome expression study performed with microarrays at baseline on liver tissue and/or PBMCs to try to find a differential gene expression able to correlate with a successful conversion and thus, to generate a set of transcriptional biomarkers potentially able to predict the result of the IS conversion on an independent cohort of liver recipients.

Detailed Description

Introduction: Immunosuppressive treatment (IS) has several and frequents adverse effects; among them are: severe infections, diabetes mellitus, arterial hypertension, osteoporosis, neurologic disorders, renal failure, dyslipemias, increased cardiovascular risk, cancer, etc. After 5 years, 18% of liver receptors develop renal failure, the risk of developing cancer is three times higher after LT and 30% of liver graft receptors previously infected by hepatitis C virus (HCV) have cirrhosis 5 years after LT, probably because of the effect of IS on viral kinetics. An ideal situation would be that liver transplant recipients receive enough IS to inhibit the immune response against the allograft, while avoiding an excessive effect over the capacity of the immune system to recognize pathogens, tumoral cells and minimizing the adverse effects or even more, the indefinite graft acceptance in the complete absence of IS, concept that in clinic in called operational tolerance (OT). OT occurs in around 20% of liver recipients. So although the potential benefit is important it affects just a small fraction of liver recipients. A different but related strategy has been evaluated in several trials in the past, and consist in to change from an IS based on calcineurin inhibitors (CNI) to another less intense based on mofetil mycophenolate (MMF), which is known to have less adverse effects, preserve renal function and do not affect the function and proliferation of T regulatory cells, which are involved in the development of OT. In a recent study (in press), the investigators performed an IS withdrawal to over a hundred liver recipients and the investigators found that those who were classified as operationally tolerant (40%) where those with a longer time elapsed since LT to IS withdrawal, those who received lower doses of CNI and those who received MMF monotherapy. The investigators were able also to discriminate between operationally tolerant liver recipients and those who developed a rejection based on its differential gene expression (evaluated by whole genome microarray) just before the ISwithdrawal.

Study's aim: to perform IS conversion from CNI to MMF monotherapy and look for transcriptional biomarkers employing whole a genome expression study performed with microarrays at baseline on liver tissue and PBMCs to try to find a set differentially expressed genes able to correlate with a successful conversion and thus, to generate a set of transcriptional biomarkers potentially able to predict the result of the IS conversion on an independent cohort of liver recipients.

Methods: Forty patients will be recruited among our cohort of liver transplant recipients. The study will last 48 weeks. Inclusion criteria will be a) liver transplantation more than 2 years ago, b) stable graft function, b) no history of autoimmune liver disease, c) absence of rejection in the last 12 months, d) Use of calcineurin inhibitors (CNI) as monotherapy, e)absence of rejection on baseline liver biopsy, d) tacrolimus trough levels > 3 ng/ml or cyclosporine C2 levels > 30 ng/ml, e) signature of the informed consent form. After screening procedure mycophenolate mofetil will be started (week -4) at a dose of 500 mg twice a day for two weeks and then (week -2) increased to 1000 mg twice a day and CNI will be reduced at the 50% of the initial dose. After two weeks (week 0) CNI will be completely discontinued(complete IS conversion). The investigators will follow up patients every 4 weeks up to 48 weeks after the complete IS conversion. The complete study period will last 52 weeks. At baseline mRNA fron liver samples and peripheral blood mononuclear cells will be isolated. This mRNA will be used to evaluate whole genome expression using Affimetrix microarrays. Besides, T regulatory cells frequency will be measured using peripheral blood cell immunophenotyping at baseline and at the end of the follow up. Clinical variables will be evaluated to determined the evolution of renal function and other cardiovascular risk factors.

Expected results: The investigators expect that at the end of the study most of the recipients will have been able to have a successful rejection and a minor group (around 30%) will not be able to do it because of rejection. Then baseline mRNA samples will be used to perform whole genome microarrays. Using bioinformatics procedures the investigators will make an attempt to establish a differential gene expression among those with a successful conversion and those that develop rejection. This will allow the investigators to determine the smallest set of genes able to discriminate between those patients. Gene expression will be also correlated with peripheral blood cell immunophenotyping and clinical variables.

Conditions

Gene Expression; Immunosuppression Conversion; Liver Transplantation

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: DIAGNOSTIC
• Blinding Strategy: NONE

Study Groups

Conversion arm

After screening procedure mycophenolate mofetil will be started (week -4) at a dose of 500 mg twice a day for two weeks and then (week -2) increased to 1000 mg twice a day and CNI will be reduced at the 50% of the initial dose. After two weeks (week 0) CNI will be completely discontinued (complete IS conversion). The investigators will follow up patients every 4 weeks up to 48 weeks after the complete IS conversion.

Group Type: EXPERIMENTAL

conversion from CNI to MMF

Intervention Type: DRUG

After screening procedure mycophenolate mofetil will be started (week -4) at a dose of 500 mg twice a day for two weeks and then (week -2) increased to 1000 mg twice a day and CNI will be reduced at the 50% of the initial dose. After two weeks (week 0) CNI will be completely discontinued (complete IS conversion). The investigators will follow up patients every 4 weeks up to 48 weeks after the complete IS conversion.

Interventions

conversion from CNI to MMF

After screening procedure mycophenolate mofetil will be started (week -4) at a dose of 500 mg twice a day for two weeks and then (week -2) increased to 1000 mg twice a day and CNI will be reduced at the 50% of the initial dose. After two weeks (week 0) CNI will be completely discontinued (complete IS conversion). The investigators will follow up patients every 4 weeks up to 48 weeks after the complete IS conversion.

Intervention Type: DRUG

Other Intervention Names

Conversion

Eligibility Criteria

Inclusion Criteria

• Liver transplantation more than 2 years ago
• Stable graft function
• No history of autoimmune liver disease
• Absence of rejection in the last 12 months
• IS regime: calcineurin inhibitors (CNI) as monotherapy
• Absence of rejection in the baseline liver biopsy
• Signature of the informed consent form

Exclusion Criteria

• total white cell count ≤ 2 x 109/L
• hemoglobin < 7.0 g/L
• platelet count ≤ 50x x 109/L
• systemic infection requiring therapy
• pregnancy

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Pontificia Universidad Catolica de Chile

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Carlos E Benitez, MD

Role: PRINCIPAL_INVESTIGATOR

Gastroenterology Department. Pontificia Universidad Católica de Chile

Locations

Gastroenterology Department, Pontificia Universidad Catolica de Chile

Santiago, Santiago, RM, Chile

Site Status: RECRUITING

Countries

Chile

Central Contacts

Carlos E Benitez, MD

Role: CONTACT

cbenitez@med.puc.cl

56-02-3543820 ext. 3880

Facility Contacts

Carlos E Benitez, MD

Role: primary

cbenitezc@med.puc.cl

56-02-3543820 ext. 3880

References

Mells G, Neuberger J. Long-term care of the liver allograft recipient. Semin Liver Dis. 2009 Feb;29(1):102-20. doi: 10.1055/s-0029-1192059. Epub 2009 Feb 23.

Reference Type: BACKGROUND

PMID: 19235663 (View on PubMed)

Fishman JA. Infection in solid-organ transplant recipients. N Engl J Med. 2007 Dec 20;357(25):2601-14. doi: 10.1056/NEJMra064928. No abstract available.

Reference Type: BACKGROUND

PMID: 18094380 (View on PubMed)

Martinez-Llordella M, Lozano JJ, Puig-Pey I, Orlando G, Tisone G, Lerut J, Benitez C, Pons JA, Parrilla P, Ramirez P, Bruguera M, Rimola A, Sanchez-Fueyo A. Using transcriptional profiling to develop a diagnostic test of operational tolerance in liver transplant recipients. J Clin Invest. 2008 Aug;118(8):2845-57. doi: 10.1172/JCI35342.

Reference Type: BACKGROUND

PMID: 18654667 (View on PubMed)

Demirkiran A, Sewgobind VD, van der Weijde J, Kok A, Baan CC, Kwekkeboom J, Tilanus HW, Metselaar HJ, van der Laan LJ. Conversion from calcineurin inhibitor to mycophenolate mofetil-based immunosuppression changes the frequency and phenotype of CD4+FOXP3+ regulatory T cells. Transplantation. 2009 Apr 15;87(7):1062-8. doi: 10.1097/TP.0b013e31819d2032.

Reference Type: BACKGROUND

PMID: 19352129 (View on PubMed)

Farkas SA, Schnitzbauer AA, Kirchner G, Obed A, Banas B, Schlitt HJ. Calcineurin inhibitor minimization protocols in liver transplantation. Transpl Int. 2009 Jan;22(1):49-60. doi: 10.1111/j.1432-2277.2008.00796.x.

Reference Type: BACKGROUND

PMID: 19121146 (View on PubMed)

Norero B, Serrano CA, Sanchez-Fueyo A, Duarte I, Torres J, Ocquetau M, Barrera F, Arrese M, Soza A, Benitez C. Conversion to mycophenolate mofetil monotherapy in liver recipients: Calcineurin inhibitor levels are key. Ann Hepatol. 2017 Jan-Feb 2017;16(1):94-106. doi: 10.5604/16652681.1226820.

Reference Type: DERIVED

PMID: 28051798 (View on PubMed)

Other Identifiers

10-071

Identifier Type: -

Identifier Source: org_study_id