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Original Articles

Lifitegrast ophthalmic solution for treatment of ocular chronic graft-versus-host disease

, ORCID Icon, , , , & show all
Pages 869-874 | Received 14 Aug 2019, Accepted 13 Nov 2019, Published online: 25 Nov 2019
 

Abstract

Ocular chronic graft-versus-host disease (oGVHD) is a relatively common complication that occurs following allogeneic hematopoietic cell transplantation. Keratoconjunctivitis sicca (KCS) is the most common manifestation of oGVHD. Lifitegrast is a lymphocyte function-associated antigen-1 antagonist approved to reduce inflammation and symptoms in patients with dry eye disease. We evaluated the efficacy and safety of lifitegrast (5% ophthalmic solution) in patients with ocular GVHD in a single-institution retrospective cohort study of eighteen allogeneic transplant recipients who received topical lifitegrast for oGVHD treatment. The outcome of interest was improvement in oGVHD severity score by National Institutes of Health (NIH) criteria. Lifitegrast was well-tolerated and no serious adverse events were observed. Lifitegrast significantly improved NIH severity scores in 8 (44%) patients. The findings of this study suggest lifitegrast is safe, well-tolerated and is an effective option for oGVHD manifesting as KCS. Prospective evaluation is warranted to confirm efficacy of lifitegrast in this population.

    Highlights

  1. In this single-institution retrospective cohort study of eighteen patients who received allogeneic transplant between 2013 and 2018, and received topical lifitegrast for treatment of ocular GVHD, the results demonstrate that lifitegrast eye drops were well-tolerated and led to improvement in symptoms of KCS in 8 (44%) patients.

  2. Lifitegrast has the potential to fulfill an unmet need in allogeneic transplant patients with ocular GVHD. Further prospective study is warranted for confirmation.

Author contributions

SC and MH designed the study, SC and JHJ acquired the data, SC analyzed the data, and SC drafted the manuscript. JEC, KZ, NNS, PNH and MH reviewed and critically revised the manuscript. All authors approved the final manuscript.

Disclosure statement

No potential conflict of interest was reported by the authors.

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