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Prevalence and Clinical Patterns of Ocular Complications Associated With Anti-PD-1/PD-L1 Anticancer Immunotherapy
Karen Bitton1, Jean-Marie Michot2, Emmanuel Barreau3
1Service d'Ophtalmologie, DHU Vision & Handicaps, Centre de référence pour les maladies rares en ophtalmologie (OPHTARA), Hôpital Bicêtre, Assistance Publique Hôpitaux de Paris, Le Kremlin-Bicêtre, France; Université Paris-Sud, Le Kremlin-Bicêtre, France.
Purpose:
Immune checkpoint inhibitors (ICI) targeting the programmed cell death protein 1 (PD-1), or its ligand PD-L1, are the mainstay of metastatic cancer treatment. Patients receiving these treatments may develop immune-related adverse events (irAEs). This study aimed to estimate the prevalence and describe the clinical patterns of moderate-to-severe ocular irAEs-associated with anti-PD-(L)1 treatment.
Design:
Prospective case series.
Methods:
This study included patients recruited via (1) a single-center prospective cohort and (2) a national pharmacovigilance registry between June 2014 and March 2018, and focused on patients with moderate-to-severe ocular irAEs following anti-PD-(L)1. All patients underwent a comprehensive ophthalmologic assessment. The main outcome measure was the prevalence of moderate-to-severe ocular irAEs.
Results:
Of a total of 745 patients included in the prospective cohort, 3 developed moderate-to-severe ocular irAEs, providing a prevalence of 0.4% and an incidence of 0.7 per 1000 patient-months of treatment. An additional 5 cases of moderate-to-severe ocular irAEs were reported through the national registry. From these 8 patients, 5 presented with intraocular inflammation, 2 with ocular surface disease, and 1 with orbital myopathy. Five patients (62.5%) experienced additional extraophthalmologic irAEs. Ocular irAEs led to permanent discontinuation of anti-PD-(L)1 in 4 patients. Treatment by local and/or systemic corticosteroids allowed resolution or control of the ocular symptoms in 7 of 8 patients.
Conclusion:
Although uncommon, anti-PD-(L)1-associated ocular complications may be sight-threatening and lead to discontinuation of anti-PD-(L)1 treatments. Patients complaining of eye problems while receiving ICI treatment should immediately be seen by an ophthalmologist.
Insights
Immune checkpoint inhibitors (ICI) can cause rare but serious eye problems. Early ophthalmologic evaluation is crucial for patients experiencing vision changes during ICI therapy to prevent vision loss.
Area of Science:
- Oncology
- Ophthalmology
- Immunology
Background:
- Immune checkpoint inhibitors (ICIs) targeting programmed cell death protein 1 (PD-1) or its ligand PD-L1 are standard treatments for metastatic cancers.
- Patients undergoing ICI therapy are at risk of developing immune-related adverse events (irAEs).
Purpose of the Study:
- To determine the prevalence of moderate-to-severe ocular irAEs in patients treated with anti-PD-(L)1 therapy.
- To describe the clinical characteristics and outcomes of these ocular irAEs.
Main Methods:
- A prospective case series design was employed, combining data from a single-center prospective cohort and a national pharmacovigilance registry.
- Patients with moderate-to-severe ocular irAEs following anti-PD-(L)1 treatment underwent comprehensive ophthalmologic assessments.
- Data were collected between June 2014 and March 2018.
Main Results:
- The prevalence of moderate-to-severe ocular irAEs was 0.4% in the prospective cohort (3 out of 745 patients).
- Eight patients in total presented with various ocular conditions, including intraocular inflammation, ocular surface disease, and orbital myopathy.
- Ocular irAEs necessitated permanent discontinuation of anti-PD-(L)1 treatment in 4 patients, though 7 out of 8 patients responded to corticosteroid treatment.
Conclusions:
- Anti-PD-(L)1-associated ocular complications, while uncommon, can be sight-threatening and may lead to treatment cessation.
- Prompt ophthalmologic consultation is essential for patients on ICI therapy who report eye-related symptoms.
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