A randomized phase 2 trial of oral vitamin A for graft-versus-host disease in children and young adults

Author:

Khandelwal Pooja12ORCID,Langenberg Lucille12,Luebbering Nathan12,Lake Kelly E.12ORCID,Butcher Abigail1,Bota Kylie12,Ramos Kristie N.12,Taggart Cynthia12,Choe Hannah3,Vasu Sumithira3,Teusink-Cross Ashley24,Koo Jane12ORCID,Wallace Gregory12,Romick-Rosendale Lindsey25,Watanabe-Chailland Miki25,Haslam David B.26ORCID,Lane Adam12,Davies Stella M.12

Affiliation:

1. 1Division of Bone Marrow Transplant and Immune Deficiency, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH

2. 2Department of Pediatrics, University of Cincinnati College of Medicine, Cincinnati OH

3. 3Division of Hematology, The Ohio State Comprehensive Cancer Center, Columbus OH

4. 4Division of Pharmacy, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH

5. 5Division of Pathology, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH

6. 6Divison of Infectious Diseases, Cincinnati Children’s Hospital Medical Center, Cincinnati, OH

Abstract

Abstract Vitamin A plays a key role in the maintenance of gastrointestinal homeostasis and promotes a tolerogenic phenotype in tissue resident macrophages. We conducted a prospective randomized double-blinded placebo-controlled clinical trial in which 80 recipients of hematopoietic stem cell transplantation (HSCT) were randomized 1:1 to receive pretransplant high-dose vitamin A or placebo. A single oral dose of vitamin A of 4000 IU/kg, maximum 250 000 IU was given before conditioning. The primary end point was incidence of acute graft-versus-host disease (GVHD) at day +100. In an intent-to-treat analysis, incidence of acute GVHD was 12.5% in the vitamin A arm and 20% in the placebo arm (P = .5). Incidence of acute gastrointestinal (GI) GVHD was 2.5% in the vitamin A arm (P = .09) and 12.5% in the placebo arm at day +180. Incidence of chronic GVHD was 5% in the vitamin A arm and 15% in the placebo arm (P = .02) at 1 year. In an “as treated” analysis, cumulative incidence of acute GI GVHD at day +180 was 0% and 12.5% in recipients of vitamin A and placebo, respectively (P = .02), and cumulative incidence of chronic GVHD was 2.7% and 15% in recipients of vitamin A and placebo, respectively (P = .01). The only possibly attributable toxicity was asymptomatic grade 3 hyperbilirubinemia in 1 recipient of vitamin A at day +30, which self-resolved. Absolute CCR9+ CD8+ effector memory T cells, reflecting gut T-cell trafficking, were lower in the vitamin A arm at day +30 after HSCT (P = .01). Levels of serum amyloid A-1, a vitamin A transport protein with proinflammatory effects, were lower in the vitamin A arm. The vitamin A arm had lower interleukin-6 (IL-6), IL-8, and suppressor of tumorigenicity 2 levels and likely a more favorable gut microbiome and short chain fatty acids. Pre-HSCT oral vitamin A is inexpensive, has low toxicity, and reduces GVHD. This trial was registered at www.ClinicalTrials.gov as NCT03202849.

Publisher

American Society of Hematology

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1. Vitamin A keeps the GVHD away?;Blood;2024-03-21

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