4.2 Article

Bandage Soft Contact Lenses for Ocular Graft-versus-Host Disease

Journal

BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION
Volume 21, Issue 11, Pages 2002-2007

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/j.bbmt.2015.07.013

Keywords

Contact lens; Dry eye disease; Graft-versus-host disease; Hematopoietic cell transplantation; Treatment

Funding

  1. NIH [U54 CA163438]
  2. initiative of the Office of Rare Diseases Research (ORDR), NCATS
  3. JSPS KAKENHI [15K19563]
  4. Friends of Leukemia Research Fund
  5. Grants-in-Aid for Scientific Research [15K19563] Funding Source: KAKEN

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To examine safety and efficacy of bandage soft contact lenses (BSCLs) for ocular chronic graft-versus host disease (GVHD), we conducted a phase II clinical trial. Extended-wear BSCLs were applied under daily topical antibiotic prophylaxis. Patients completed standardized symptom questionnaires at enrollment and at 2 weeks, 4 weeks, and 3 months afterward. Ophthalmologic assessment was performed at enrollment, at 2 weeks, and afterward as medically needed. Assessments at follow-up were compared with baseline by paired t-test. Nineteen patients with ocular GVHD who remained symptomatic despite conventional treatments were studied. The mean Lee eye subscale score was 75.4 at enrollment and improved significantly to 63.2 at 2 weeks (P=.01), to 61.8 at 4 weeks (P=.005), and to 56.3 at 3 months (P=.02). The ocular surface disease index score and 11-point eye symptom ratings also improved significantly. According to the Lee eye subscale, clinically meaningful improvement was observed in 9 patients (47%) at 2 weeks, in 11 patients (58%) at 4 weeks, and in 9 patients (47%) at 3 months. Visual acuity improved significantly at 2 weeks compared with enrollment values. Based on slit lamp exam at 2 weeks, punctate epithelial erosions improved in 58% of the patients, showed stability in 16%, and worsened in 5%. No corneal ulceration or ocular infection occurred. BSCLs are a widely available, safe, and effective treatment option that improves manifestations of ocular GVHD in approximately 50% of patients. (C) 2015 American Society for Blood and Marrow Transplantation.

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