Download PDFPDF

Long-term efficacy and tolerability of TNFα inhibitors in the treatment of non-infectious ocular inflammation: an 8-year prospective surveillance study
  1. Srilakshmi M Sharma1,
  2. Erika Damato2,
  3. Ann E Hinchcliffe3,4,
  4. Colm D Andrews5,6,
  5. Katie Myint7,
  6. Richard Lee4,8,
  7. Andrew D Dick4,9
  1. 1 Oxford Eye Hospital, Oxford, UK
  2. 2 Ophthalmology, Addenbrooke's Hospital, Cambridge, UK
  3. 3 Bristol Eye Hospital, Bristol, UK
  4. 4 National Institute of Health Research, Biomedical Research Centre in Ophthalmology, Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology, London, UK
  5. 5 Ophthalmology, John Radcliffe Hospital, Oxford, UK
  6. 6 Eye Research Group Oxford, Oxford Eye Hospital, John Radcliffe Hospital, Oxford, UK
  7. 7 UCL Institute of Ophthalmology, London, UK
  8. 8 School of Clinical Sciences, University of Bristol, Bristol, UK
  9. 9 Ophthalmology, University of Bristol, Bristol, UK
  1. Correspondence to Dr Srilakshmi M Sharma, Oxford Eye Hospital, Oxford OX3 2TD, UK; srilakshmi.sharma@ouh.nhs.uk

Abstract

Background/Aim To report the efficacy and tolerability of antitumour necrosis factor-alpha therapy (TNF inhibitors [TNFi]) in the management of non-infectious ocular inflammation, including uveitis and scleritis, in adult patients over an 8-year period.

Materials and methods This is a prospective cohort study of infliximab and adalimumab in the treatment of non-infectious ocular inflammatory disease. 43 of 85 adult patients on TNFi (34 infliximab, 9 adalimumab) for ≥1 year with non-infectious uveitis or scleritis were followed from 2006 to 2014. Clinical assessments, medication, adverse events and history of steroid rescues were collected at 6 monthly intervals. General quality of life (Short Form Health Survey (SF-36)) and visual quality of life (Vision-related quality of life Core Measure (VCM1)) were assessed annually. Outcome measures included rate of sustained remission, rate of relapse, systemic corticosteroid reduction, adverse events, and VCM1 and SF-36 scores.

Results The median time on infliximab was 3.2 years (IQR 4.3) and on adalimumab was 2.4 years (IQR 1.8). Sustained remission was induced in 39 patients (91%) (0.5 per patient year) after a median of 1.2 years on a TNFi. 22 (51%) experienced one relapse, and 5 (12%) had two relapses. 23 (54%) had at least one adverse event; serious adverse events necessitating hospitalisation or cessation of medication occurred in four (9%) patients. 10 patients (23%) switched from the initiation of TNFi, at 1.7 years after starting, to another TNFi or another class of biologic therapy.

Conclusion TNFi treatment is associated with long-term drug-induced remission of ocular inflammation, visual stability and corticosteroid reduction. Adverse events were common and no new safety signals occurred. Relapse of inflammation occurs in half of the treated population.

  • inflammation
  • immunology
  • drugs
http://creativecommons.org/licenses/by-nc/4.0/

This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/.

Statistics from Altmetric.com

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Footnotes

  • Contributors CDA: Statistical analysis and assistance in preparation of the manuscript. ED: assisted in conducting the study, data collection and contributed to analysis. ADD: chief investigator of the study, contributed to the design of the study and edited the manuscript. AEH: coordinated the study. KM: quality of life data collation and assistance in preparation of the manuscript. RL: contributed to the design, collection of data and review of the manuscript. SMS: designed and conducted the study, was the PI of the study, interpreted the data and prepared the manuscript.

  • Funding This work was funded by Above & Beyond Charity, Bristol, UK.

  • Competing interests SMS has participated in advisory boards for AbbVie, outside the submitted work. ADD has been an external advisor for AbbVie, Novartis and Roche, outside the submitted work. ADD and SMS have participated in educational initiatives on behalf of AbbVie. SMS and ADD have received honoraria from AbbVie. All other authors have no competing interests to report.

  • Provenance and peer review Not commissioned; externally peer reviewed.

  • Data sharing statement To our knowledge, there are no unpublished data from this data set which may be made available to any other party.

Linked Articles

  • At a glance
    Frank Larkin