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RECRUITINGOBSERVATIONAL

Predicting the Quality of Response to Specific Treatments in Patients With cGVHD, PQRST Study

Predicting the Quality of Response to Specific Treatments (PQRST)

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

This trial collects clinical data and blood samples to predict the quality of response to specific treatments in patients with chronic graft-versus-host disease (cGVHD) who are about to start a new therapy. Collecting and analyzing clinical data and blood samples from patients with cGVHD before and after treatment initiation may help doctors identify changes that may predict treatment response.

Who May Be Eligible (Plain English)

Who May Qualify: - Adults age 18 or older - Prior allogeneic stem cell transplant, with any graft source, donor type, and GVHD prophylaxis - No evidence of persistent or progressive malignancy at the time of enrollment - Agrees to be evaluated at the transplant center before a new line of treatment is started (may be concurrent with the enrollment visit), and later between 2-6 weeks, 3 months and 6 months after index treatment is started or if an additional new therapy is started before 6 months - Signed, willing to sign a consent form Who Should NOT Join This Trial: - Inability to comply with study procedures - Uncontrolled psychiatric disorder - Anticipated survival \< 6 months Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Adults age 18 or older * Prior allogeneic stem cell transplant, with any graft source, donor type, and GVHD prophylaxis * No evidence of persistent or progressive malignancy at the time of enrollment * Agrees to be evaluated at the transplant center before a new line of treatment is started (may be concurrent with the enrollment visit), and later between 2-6 weeks, 3 months and 6 months after index treatment is started or if an additional new therapy is started before 6 months * Signed, informed consent Exclusion Criteria: * Inability to comply with study procedures * Uncontrolled psychiatric disorder * Anticipated survival \< 6 months

Treatments Being Tested

PROCEDURE

Biospecimen Collection

Undergo collection of blood sample

OTHER

Medical Chart Review

Review of medical chart

OTHER

Quality-of-Life Assessment

Ancillary studies

OTHER

Questionnaire Administration

Complete questionnaire

Locations (10)

University of Florida
Gainesville, Florida, United States
Moffitt Cancer Center
Tampa, Florida, United States
Dana-Farber Harvard Cancer Center
Boston, Massachusetts, United States
University of Minnesota/Masonic Cancer Center
Minneapolis, Minnesota, United States
Roswell Park Cancer Institute
Buffalo, New York, United States
Cleveland Clinic Foundation
Cleveland, Ohio, United States
UPMC Hillman Cancer Center
Pittsburgh, Pennsylvania, United States
Vanderbilt University/Ingram Cancer Center
Nashville, Tennessee, United States
Fred Hutch/University of Washington Cancer Consortium
Seattle, Washington, United States
Vancouver General Hospital/BC Cancer
Vancouver, British Columbia, Canada