Cytomegalovirus (CMV) Specific Cytotoxic T Lymphocytes (CTL) When Used for Prophylaxis Against CMV in Recipients of Allogeneic, T Cell Depleted Stem Cell Transplants

Cytomegalovirus Infections Clinical Trial

Official title:

A Phase I-II Randomized Trial to Examine the Clinical, Immunologic and Virologic Effects of CMV Specific CTL When Used for Prophylaxis Against CMV Disease in Recipients of Allogeneic, T Cell Depleted Stem Cell Transplants

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00673868
• Other study ID #: 26769
• Status: Completed
• Phase: Phase 1
• First received: May 1, 2008
• Last updated: June 30, 2017
• Start date: October 2007
• Est. completion date: August 6, 2008

Study information

• Verified date: June 2017
• Source: Milton S. Hershey Medical Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study examines the immunologic and virologic effects of prophylactic CMV specific CTL in recipients of T cell depleted stem cell transplant (TCD SCT) at Duke University Medical Center (DUMC), by measuring levels of CMV DNA and virus specific T cell precursors at intervals post-infusion.

Description:

Human cytomegalovirus (CMV) is a benign infectious agent in the normal host, but in immunocompromised individuals, such as recipients of stem cell or organ transplants, this virus is a major cause of morbidity and mortality. While pharmacologic agents exist to treat CMV disease, these medications have numerous side effects, the most serious of which is myelosuppression. Considering the risk associated with persistent infection and the potential for CMV specific CTL to restore immunity, we propose to study the immunologic and virologic effects of CMV pp65 specific CTL given to SCT recipients prophylactically, levels of CMV pp65 specific CTL and CMV DNA will be measured from CTL recipients and a control group randomized to not receive CTL.

All treatments will be given at Duke University Medical Center (DUMC).

1. Patients will have a complete set of vital signs and physical examination prior to each infusion. Pulse oximetry will be monitored prior to, during, and for 30 minutes after the T-cell infusion. Thirty minutes prior to the CTL infusion, patients will be pre-medicated with 15 mg/kg (maximum 1 g) of acetaminophen p.o. and 1.0 mg/kg diphenhydramine I.V. (maximum 50 mg). Cells will be thawed in the Cell Therapy lab at DUMC, an aliquot sent for gram stain and culture, and viability will be determined. Cells with > 70 % viability will be transferred to the clinical unit and infused over 5-10 minutes.

2. CMV CTL will be infused when available between days 30 and 40 post-transplant at a dose ranging from 2- 5 x 105 cells/kg. This dose range was established since there may be variability in the numbers of CTL expanded from these donors.

This trial intended to be a Phase 1/2 trial, but it never progressed to Phase 2 before completion.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 2
• Est. completion date: August 6, 2008
• Est. primary completion date: August 6, 2008
• Accepts healthy volunteers: No
• Gender: All
• Age group: 2 Years to 65 Years

Eligibility

Inclusion Criteria:

• Any allogeneic stem cell transplant recipient > 2 years of age who is CMV sero-positive and has a CMV sero-positive donor,

• Bilirubin < 2.0 mg/dl; SGOT/SGPT < 2.5 X normal.

• Creatinine clearance > 50 cc/min as estimated by patient's serum creatinine, weight, and age.

• Pulse oximetry > 95% on no supplemental oxygen.

• ECOG performance status < 2; for patients, 16 years of age, Lansky performance status >70%.

Exclusion Criteria:

• Sero-negative patients with a history of GVHD of grade II or greater by the Glucksberg crireria (protocol Appendix I) at or prior to day +30 of current stem cell transplant are excluded.

• Patients who have received a prior stem cell transplant are excluded.

• Patients who are moribund or who because of cardiac, pulmonary, renal, hepatic or neurologic dysfunction are not expected to survive one month.

• Subjects receiving systemic immunosuppressive agents for the treatment of GVHD at the time of the CTL infusion will be excluded from receiving CTL, and subjects randomized to not receive CTL will also be removed from study if at the time of the CTL infusion they require systemic immunosuppression for treatment of GVHD

• Donors must be negative for HIV-1, HIV-2, and HTLV-2, and have passed all screening tests for hepatitis.

Related Conditions & MeSH terms

• Cytomegalovirus Infections

Intervention

Biological:
• CMV Specific Cytotoxic T Lymphocytes
CMV Specific Cytotoxic T Lymphocytes will be infused between days 30 and 40 post-transplant at a dose ranging from 2- 5 x e5 cells/kg.

Locations

Country	Name	City	State
United States	Penn State University	Hershey	Pennsylvania

Sponsors (1)

Lead Sponsor	Collaborator
Milton S. Hershey Medical Center

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary objective is to characterize CMV specific immunity in subjects receiving and in those randomized to not receive CMV CTL. We will characterize CMV CTLp frequencies and bulk cytotoxicity at days 30 and 60 post infusion.		one year
Secondary	To characterize the time to develop CMV specific immunity in pts. receiving and not receiving CTL by assessing CMV CTL		one year
Secondary	To determine the CMV epitopes recognized by donors		one year
Secondary	To characterize the levels of CMV DNA in recipients of CMV CTL and non CTL		one year