Cell Mediated Immunity for Secondary Prophylaxis in CMV SOT Patients

Cytomegalovirus Viraemia Clinical Trial

— Q-CMV  

Official title:

Cell Mediated Immunity as a Guide for Secondary Prophylaxis in SOT Patients With CMV Infection

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02370758
• Other study ID #: UHN-CMV-001
• Status: Completed
• Phase: N/A
• First received: February 18, 2015
• Last updated: September 20, 2017
• Start date: November 2014
• Est. completion date: June 16, 2017

Study information

• Verified date: September 2017
• Source: University Health Network, Toronto
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study will evaluate whether a test for Cytomegalovirus (CMV) specific cell-mediated immunity can be used to determine whether patients who complete a course of therapy for CMV viremia need secondary antiviral prophylaxis. Subjects that have negative CMV CMI will receive antiviral prophylaxis for 2 months and those with positive CMV CMI will have their prophylaxis stopped.

Description:

Cytomegalovirus (CMV) is the most important infection in transplant patients and it is a common cause of illness in patients who have undergone a transplant. Serious infections due to CMV can affect many parts of the body including the lungs, the gut, and the liver; when CMV infection becomes serious enough to cause symptoms, it is called CMV disease. Some patients require treatment while others will clear the virus on their own.

QuantiFERON-CMV (QFT-CMV) is a blood test that measures CMV-specific cell-mediated immunity. This test was able to predict that patients with low cell-mediated immunity are at greater risk for developing CMV disease. In this study, QFT-CMV will be used to make a decision regarding CMV treatment. The QFT-CMV test will be performed at the first detection of CMV, at end of antiviral therapy and one month post-therapy. The end-of-therapy results will be available to clinicians and study investigators within one week of collection. Based on the result, a decision will be made to continue with prolonged antiviral therapy. Patients that show weak cell-mediated immunity against CMV will be given secondary antiviral prophylaxis, while patients with good cell-mediated immunity will have their therapy stopped. Patients will continue to be monitored three months after the last QFT-CMV test for recurrent CMV viremia.

This study will also attempt to evaluate the predictive value of the QuantiFERON-Monitor (QFT-Monitor) assay. QFT-Monitor is a recently developed non-pathogen specific immune assay: it is based on immune activation of both innate and adaptive immunity. The investigators hypothesize that stimulation of both the innate and adaptive immunity may predict global immune function and also be predictive of CMV reactivation. The investigators plan to perform the QFT-Monitor assay in parallel to the QFT-CMV test to determine the test characteristics and cut-off values in predicting global immune function. This test will be collected and tested in batches. Therefore, the results will not influence clinical decisions.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 32
• Est. completion date: June 16, 2017
• Est. primary completion date: September 2016
• Accepts healthy volunteers: No
• Gender: All
• Age group: N/A and older

Eligibility

Inclusion Criteria:

• Adult solid organ transplant (SOT) recipient on at least one immunosuppressive medication

• Starting therapy for new onset asymptomatic CMV viremia OR starting therapy for new onset CMV disease

• CMV viral load = 1000 IU/mL

Exclusion Criteria:

• Known ganciclovir-resistant CMV

• Known intolerance to valganciclovir or ganciclovir

• Unable to comply with protocol

Related Conditions & MeSH terms

• Cytomegalovirus Viraemia
• Viremia

Intervention

Drug:
• Valganciclovir or Ganciclovir

Locations

Country	Name	City	State
Canada	University Health Network, Toronto General Hospital, Multi-Organ Transplant	Toronto	Ontario

Sponsors (1)

Lead Sponsor	Collaborator
University Health Network, Toronto

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Virologic recurrence or disease recurrence		6 months