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Biomarkers in Predicting Response in Patients With Graft-Versus-Host Disease Undergoing Extracorporeal Photophoresis | Clinical Trials | Clareo Health

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Biomarkers in Predicting Response in Patients With Graft-Versus-Host Disease Undergoing Extracorporeal Photophoresis

T-regulatory Homing Subsets as a Predictor of Response in GVHD Treated With Extracorporeal Photopheresis

NCT01324908•Vanderbilt-Ingram Cancer Center

View on ClinicalTrials.gov

Summary

This clinical trial studies biomarkers in predicting response in patients with graft-versus-host disease (GVHD) undergoing extracorporeal photopheresis (ECP). ECP treats the patient's blood with ultraviolet light outside the body and kills the white blood cells before returning blood back into the patient's body. Studying samples of blood from patients with GVHD may help doctors identify and learn more about biomarkers related to GVHD.

Detailed Description

PRIMARY OBJECTIVE: I. To show that extracorporeal photopheresis (ECP)increases skin and gut homing T regulatory (T-reg) cells in patients with GVHD clinically responding to ECP. SECONDARY OBJECTIVES: I. Response rates of GVHD with extracorporeal photopheresis(ECP)as measured by NIH response criteria II. Incidence of T-reg cell frequency(%)with various NIH subtypes of chronic graft-versus-host disease (GVHD) III. Incidence of T-reg homing subsets(%)with various NIH subtypes of chronic graft-versus-host disease (GVHD) OUTLINE: Patients undergo ECP twice a week for 4 weeks and then twice a week every 2 weeks for 8 weeks. After completion of study treatment, patients are followed up at 2, 4, and 6 months.

Eligibility

Age

18 - No limit years

Sex

ALL

Healthy Volunteers

Inclusion Criteria

•Patients with any NIH subtype of chronic GVHD that is being treated with ECP
•Karnofsky Performance Scale (KPS) \> 60% at time of study enrollment
•Life expectancy \> 3 months
•Steroid dose not greater than 2 mg/kg prednisone equivalent at time of study enrollment
•If patient has steroid refractory GVHD (defined as worsening of GVHD after 3 days of 2 mg/kg prednisone equivalent or no improvement after 7 days of 2 mg/kg prednisone equivalent), time interval from start of steroids to initiation of ECP should not be \> 14 days
•No use of an investigational agent within 2 weeks of starting ECP
•No uncontrolled bacterial, fungal or viral disease (therapy for cytomegalovirus \[CMV\] viremia is permitted)
•No evidence of relapse or progression of underlying disease (molecular evidence of relapse/progression or mixed chimerism is permitted)
•Women of childbearing potential (WOCBP) should be willing to use 2 forms of contraception; male patients should be willing to use contraception
•Voluntary written informed consent before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the subject at any time without prejudice to future medical care

Exclusion Criteria

•Female patients who are breastfeeding or pregnant
•Patients known to be human immunodeficiency virus (HIV) positive
•Bronchiolitis obliterans as the sole indication of ECP
•Serious medical or psychiatric illness likely to interfere with participation in this clinical study
•Mechanical ventilation, renal replacement therapy, admitted in intensive care until at time of enrollment
•Stage 4 gastrointestinal GVHD as per Seattle-Glucksberg criteria

Locations (4)

Emory University

Atlanta, Georgia, United States

Dana Farber Cancer Center

Boston, Massachusetts, United States

Vanderbilt-Ingram Cancer Center

Nashville, Tennessee, United States

Virginia Commonwealth University, Massey Cancer Center

Richmond, Virginia, United States

Key Dates

Start Date

July 1, 2011

Primary Completion Date

July 28, 2017

Completion Date

November 16, 2020

Last Updated

January 14, 2021

Enrollment

ACTUAL participants

Conditions

Graft Versus Host Disease (GVHD)

Interventions

extracorporeal photopheresis

PROCEDURE

laboratory biomarker analysis

OTHER

Treatment of GVHD in Hematopoietic Stem Cell Transplant (HSCT) Recipients Using AAT Plus Corticosteroids (CS) Compared With Corticosteroids Alone

NCT04167514

Graft Versus Host Disease (GVHD)

View study

Data Source & Attribution

This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.

ClinicalTrials.gov last update: January 14, 2021Data synced to Clareo: March 29, 2026

Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.

Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.

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