Patient-reported quality of life is associated with severity of chronic graft-versus-host disease as measured by NIH criteria: report on baseline data from the Chronic GVHD Consortium

Author:

Pidala Joseph1,Kurland Brenda2,Chai Xiaoyu2,Majhail Navneet3,Weisdorf Daniel J.3,Pavletic Steven4,Cutler Corey5,Jacobsohn David6,Palmer Jeanne7,Arai Sally8,Jagasia Madan9,Lee Stephanie J.2

Affiliation:

1. Moffitt Cancer Center, Tampa, FL;

2. Fred Hutchinson Cancer Research Center, Seattle, WA;

3. University of Minnesota, Minneapolis, MN;

4. National Cancer Institute, Bethesda, MD;

5. Dana-Farber Cancer Institute, Boston, MA;

6. Children's Memorial Hospital, Chicago, IL;

7. Medical College of Wisconsin, Milwaukee, WI;

8. Stanford University, Stanford, CA; and

9. Vanderbilt University, Nashville, TN

Abstract

Abstract Quality of life (QOL) after hematopoietic cell transplantation (HCT) is compromised by chronic GVHD. In a prospectively assembled multicenter cohort of adults with chronic GVHD (n = 298), we examined the relationship between chronic GVHD severity defined by National Institutes of Health (NIH) criteria and QOL as measured by the SF-36 and FACT-BMT instruments at time of enrollment. Chronic GVHD severity was independently associated with QOL, adjusting for age. Compared with population normative data, SF-36 scores were more than a SD (10 points) lower on average for the summary physical component score (PCS) and role-physical subscale, and significantly lower (with magnitude 4-10 points) for several other subscales. Patients with moderate and severe cGVHD had PCS scores comparable with scores reported for systemic sclerosis, systemic lupus erythematosus, and multiple sclerosis, and greater impairment compared with common chronic conditions including diabetes, hypertension, and chronic lung disease. Moderate to severe cGVHD as defined by NIH criteria is associated with significant compromise in multiple QOL domains, with PCS scores in the range of other systemic autoimmune diseases. Compromised QOL provides a functional assessment of the effects of chronic GVHD, and may be measured in cGVHD clinical studies using either the SF-36 or the FACT-BMT.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

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