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Pre-clinical Evaluation of Tyrosine Kinase Inhibitors for Treatment of Acute Leukemia
Published on: September 18, 2013
Ocular side-effects associated with imatinib mesylate (Gleevec)
Frederick W Fraunfelder1, Jonathan Solomon, Brian J Druker
1Casey Eye Institute, Portland OR 97201, USA. eyedrug@ohsu.edu
Abstract:
This retrospective case series describes ocular side-effects associated with imatinib mesylate (Gleevec) and the clinical characteristics of these adverse reactions. A chart review of 104 patients on imatinib mesylate therapy from Oregon Health & Science University's Cancer Center were studied with regard to ocular side-effects. In addition, spontaneous reports from the Food and Drug Administration, the World Health Organization, and the National Registry of Drug-Induced Ocular Side-Effects databases were reviewed, including a Medline literature search. Seventy-three (70%) of the patients at OHSU developed periorbital edema and 19 patients (18%) developed epiphora after receiving imatinib mesylate. Average dose was 407.5+/-60 mg. Periorbital edema occurred an average of 68+/-48 days after initiation of therapy. WHO classification of side-effects is as follows: certain: periorbital edema; probable: epiphora; possible: extraocular muscle palsy, ptosis, blepharoconjunctivitis; unlikely: glaucoma, papilledema, retinal hemorrhage, photosensitivity, abnormal vision, and increased intraocular pressure. Periorbital edema and epiphora are the two most common ocular side-effects related to imatinib mesylate therapy. Clinical characteristics of imatinib mesylate induced periorbital edema are described. Management of ocular side-effects is conservative except in very rare cases of visually significant periorbital edema.
Insights
Imatinib mesylate (Gleevec) commonly causes ocular side effects like periorbital edema and epiphora in cancer patients. Management is typically conservative for these Gleevec side effects.
Area of Science:
- Ophthalmology
- Pharmacology
- Oncology
Background:
- Imatinib mesylate (Gleevec) is a tyrosine kinase inhibitor used in cancer therapy.
- Ocular side effects associated with imatinib mesylate are not fully characterized.
- Understanding these adverse reactions is crucial for patient management.
Purpose of the Study:
- To describe ocular side effects of imatinib mesylate.
- To detail the clinical characteristics of these adverse reactions.
- To classify the likelihood of various ocular side effects.
Main Methods:
- Retrospective case series of 104 patients on imatinib mesylate.
- Chart review at Oregon Health & Science University's Cancer Center.
- Review of spontaneous reports (FDA, WHO) and Medline literature search.
Main Results:
- 70% of patients developed periorbital edema; 18% developed epiphora.
- Periorbital edema occurred at an average of 68 days post-initiation.
- WHO classification: Certain - periorbital edema; Probable - epiphora.
Conclusions:
- Periorbital edema and epiphora are the most frequent ocular side effects of imatinib mesylate.
- Clinical characteristics of imatinib-induced periorbital edema are described.
- Ocular side effect management is generally conservative.
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