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Ocular surface toxicity of depatuxizumab mafoditin (ABT-414): case reports
Carlos Rocha-de-Lossada1, Carmen Alba Linero1, Álvaro Santos Ortega1
1Ophthalmology Department, Hospital Regional Universitario de Málaga, Málaga, Spain.
Abstract:
The purpose of this study is to report the clinical features and outcomes of ocular surface toxicity following depatuxizumab mafoditin (ABT-414) therapy for unresectable glioblastoma. Ocular signs and symptoms of three patients treated with ABT-414 during a phase III trial for glioblastoma multiforme were evaluated. Both eyes of all patients were damaged during the week after the first infusion of the ABT-414 molecule. In all patients, mild-to-moderate keratitis could be ascertained, along with decreased visual acuity and blurred vision, as well as foreign-body sensation and redness. Symptoms and visual acuity improved 4 weeks. In conclusion, ABT-414 therapy may cause transient ocular surface toxicity. The initiation of artificial tears and lubricant ointment was enough to control the ocular surface signs and symptoms. A multidisciplinary approach, complete ophthalmologic monitorization, and elaboration of protocols are required to adequately manage these patients.
Insights
Depatuxizumab mafoditin (ABT-414) therapy for glioblastoma can cause temporary ocular surface toxicity, including keratitis and blurred vision. Symptoms resolved within four weeks with artificial tears and lubricant ointment.
Area of Science:
- Ophthalmology
- Oncology
- Pharmacology
Background:
- Glioblastoma multiforme is an aggressive brain tumor.
- Depatuxizumab mafoditin (ABT-414) is an investigational antibody-drug conjugate targeting EGFR. It is used in treating unresectable glioblastoma.
Observation:
- Three patients receiving ABT-414 for glioblastoma experienced ocular surface toxicity.
- Ocular symptoms including keratitis, decreased visual acuity, blurred vision, foreign-body sensation, and redness appeared within a week of the first infusion.
Findings:
- The ocular toxicity was mild-to-moderate and transient, with symptoms and visual acuity improving within four weeks.
- Artificial tears and lubricant ointment were sufficient to manage the ocular surface signs and symptoms.
Implications:
- ABT-414 therapy may induce transient ocular surface toxicity.
- Ophthalmologic monitoring and established management protocols are crucial for patients undergoing ABT-414 treatment.
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