Diagnosis of Acute Rejection in Renal Transplant Patients by Urine Mass Spectrometry

Rejection of Renal Transplant Clinical Trial

Official title:

Non-invasive Diagnosis of Acute Rejection in Renal Transplant Patients Using Mass Spectrometry of Urine Samples - a Multicentre Diagnostic Phase III Trial

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT01315067
• Other study ID #: MS-GW4/6-1
• Status: Completed
• Phase: N/A
• First received: March 14, 2011
• Last updated: August 9, 2017
• Start date: October 2011
• Est. completion date: June 15, 2017

Study information

• Verified date: August 2017
• Source: Hannover Medical School
• Contact: n/a
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Reliable and timely detection of acute rejections in renal transplant patients is important to preserve the graft function and to prevent premature graft failure. The current gold standard for the rejection diagnosis is a renal biopsy which is usually performed upon an unexplained decline in the graft function (determined by serum creatinine or clearance). Because of the insensitivity of creatinine determinations and the invasiveness of renal biopsies, non-invasive tests have been suggested to diagnose acute rejection including mass spectrometry (MS) analysis of urine samples.

The ability of MS analysis to detect acute rejection has been demonstrated in small studies on selected patients but evidence is lacking that this test is efficacious in the routine setting of the post-transplant patient care. Based on our previous work that established urine peptide sets for acute rejection by MS, a prospective, multicentre diagnostic phase III study will be executed.

The aim of the study is to prove that this test is as equally effective as the allograft biopsy to detect acute rejection in patients that undergo a biopsy for unexplained renal dysfunction. The perspective of this approach is that the test could be used either in place of the biopsy or as decision guidance whether a biopsy is necessary to confirm the presence of rejection. Another perspective is that the MS test (respectively, a simplified test system derived from this method) could be used in the regular post-transplant surveillance for acute rejection, in place of the relatively insensitive procedure with periodic monitoring of the graft function by creatinine determinations.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 600
• Est. completion date: June 15, 2017
• Est. primary completion date: March 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Adult patients with a kidney or combined kidney/pancreas transplantation

• Unexplained renal allograft dysfunction within the first year of transplantation

• Renal allograft biopsy, which is clinically indicated to verify or exclude an acute rejection

Exclusion Criteria:

• Lacking consent of the patient to participate in the study

Related Conditions & MeSH terms

• Rejection of Renal Transplant

Locations

Country	Name	City	State
Germany	RTW University of Aachen	Aachen
Germany	Charite Universitätsmedizin Berlin	Berlin
Germany	University of Erlangen-Nuremberg	Erlangen
Germany	Universitätsklinikum Essen	Essen
Germany	Hannover Medical School	Hannover
Germany	Universitätsklinikum Jena	Jena
Germany	Kliniken der Stadt Köln gGmbH	Köln
Germany	Ludwig-Maximilians-Universitätsklinik München	München

Sponsors (1)

Lead Sponsor	Collaborator
Hannover Medical School

Country where clinical trial is conducted

Germany, 

References & Publications (2)

Metzger J, Chatzikyrkou C, Broecker V, Schiffer E, Jaensch L, Iphoefer A, Mengel M, Mullen W, Mischak H, Haller H, Gwinner W. Diagnosis of subclinical and clinical acute T-cell-mediated rejection in renal transplant patients by urinary proteome analysis. Proteomics Clin Appl. 2011 Jun;5(5-6):322-33. doi: 10.1002/prca.201000153. Epub 2011 Apr 29. — View Citation

Wittke S, Haubitz M, Walden M, Rohde F, Schwarz A, Mengel M, Mischak H, Haller H, Gwinner W. Detection of acute tubulointerstitial rejection by proteomic analysis of urinary samples in renal transplant recipients. Am J Transplant. 2005 Oct;5(10):2479-88. — View Citation

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Ability of the urine mass spectrometry test to diagnose acute renal allograft rejection, compared to the gold standard 'allograft biopsy'	In patients with unexplained renal allograft dysfunction who get an allograft biopsy to clarify if an acute rejection is present, a simultaneous urine sample will be taken.; The peptide pattern of this urine sample is analyzed by mass spectrometry and a diagnosis is made (rejection present/not present) based on a pre-defined peptide pattern which was established to detect acute allograft rejection.; In the primary outcome analysis, the sensitivity and specificity of the rejection diagnosis by the urine test is compared to the diagnosis made by the allograft biopsy.	Results of the urine test will be assessed in relation to the simultaneously performed allograft biopsy (1 day)
Secondary	Sensitivity and specificity of the urine test to diagnose acute renal allograft rejection in subgroups with different severity grades of the rejection	Sensitivity/specificity measures for the urine test will be determined in subgroups of patients with different severity of the rejection. Severity grading is based on the pathomorphological classification of the rejection (according to the BANFF classification) and on the functional impairment of the allograft at the time of rejection diagnosis.	Results of the urine test will be assessed in relation to the simultaneously performed allograft biopsy (1 day)
Secondary	Sensitivity and specificity of the urine test to diagnose acute renal allograft rejection in subgroups with kidney transplantation alone and with combined pancreas/kidney transplantation	Sensitivity/specificity measures for the urine test will be determined in subgroups of patients who have a kidney transplant or a combined pancreas/kidney transplant.	Results of the urine test will be assessed in relation to the simultaneously performed allograft biopsy (1 day)
Secondary	Sensitivity and specificity of the urine test to diagnose acute renal allograft rejection in subgroups with concurrent infection	Sensitivity/specificity measures for the urine test will be determined in subgroups of patients who have concurrent infections at the time of the biopsy and urine sampling such as cytomegaly virus, polyoma virus, and urinary tract infection. The analysis intends to identify potential interference of these conditions with the urine mass spectrometry test.	Results of the urine test will be assessed in relation to the simultaneously performed allograft biopsy (1 day)