| Literature DB >> 21689773 |
Andrew L Gilman1, Kirk R Schultz, Frederick D Goldman, George E Sale, Mark D Krailo, Zhengjia Chen, Bryan Langholz, David A Jacobsohn, Ka-Wah Chan, Robin E Ryan, Michael Kellick, Steven M Neudorf, Kamar Godder, Eric S Sandler, Indira Sahdev, Stephan A Grupp, Jean E Sanders, Donna A Wall.
Abstract
The Children's Oncology Group conducted a multicenter Phase III trial for chronic graft-versus-host disease (cGVHD). The double-blind, placebo-controlled, randomized study evaluated hydroxychloroquine added to standard therapy for children with newly diagnosed cGVHD. The study also used a novel grading and response scoring system and evaluated clinical laboratory correlates of cGVHD. The primary endpoint was complete response (CR) after 9 months of therapy. Fifty-four patients (27 on each arm) were enrolled before closure because of slow accrual. The CR rate was 28% in the hydroxychloroquine arm versus 33% in the placebo arm (odds ratio [OR] = 0.77, 95% confidence interval [CI]: 0.20-2.93, P = .75) for 42 evaluable patients. For 41 patients with severity assessment at enrollment, 20 (49%) were severe and 18 (44%) moderate according to the National Institutes of Health Consensus Conference global scoring system. The CR rate was 15% for severe cGVHD and 44% for moderate cGVHD (OR = 0.24, 95% CI: 0.05-1.06, P = .07). Although the study could not resolve the primary question, it provided important information for future cGVHD study design in this population.Entities:
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Year: 2011 PMID: 21689773 PMCID: PMC4627789 DOI: 10.1016/j.bbmt.2011.05.016
Source DB: PubMed Journal: Biol Blood Marrow Transplant ISSN: 1083-8791 Impact factor: 5.742