Imatinib mesylate (Gleevec) induced unilateral optic disc edema

Optom Vis Sci. 2012 Oct;89(10):e16-22. doi: 10.1097/OPX.0b013e318269111d.

Abstract

Purpose: Imatinib mesylate (Gleevec) is a chemotherapy medication developed to treat chronic myelogenous leukemia as well as gastrointestinal stromal tumors (Savage, N Engl J Med 2002;346:683-93). Ocular side effects are commonly reported with the use of imatinib mesylate, such as periorbital edema and epiphora. More serious ocular side effects, such as optic disc edema, are rarely reported.

Case report: This case is of a patient who presented with monocular painless loss of vision in the left eye from a previously documented 20/20 to 20/70 shortly after starting treatment with imatinib mesylate.

Results: Every aspect of the ocular presentation and clinical history were addressed to unveil the cause of the disc edema. After ruling out all other causes, the patient was later diagnosed with unilateral optic disc edema as a related side effect of the toxicity from imatinib mesylate.

Conclusions: The properties of imatinib mesylate and the possible etiology of secondary optic disc edema are discussed. This study aims to highlight the importance of systemic medications review for possible etiology of ocular disease as well as the multidisciplinary approach to managing oncology patients with ocular side effects.

Publication types

  • Case Reports

MeSH terms

  • Aged
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / therapeutic use
  • Benzamides
  • Diagnosis, Differential
  • Follow-Up Studies
  • Gastrointestinal Neoplasms / drug therapy
  • Gastrointestinal Stromal Tumors / drug therapy
  • Humans
  • Imatinib Mesylate
  • Male
  • Optic Disk / drug effects
  • Optic Disk / pathology*
  • Papilledema / chemically induced*
  • Papilledema / diagnosis
  • Piperazines / adverse effects*
  • Piperazines / therapeutic use
  • Protein-Tyrosine Kinases / antagonists & inhibitors
  • Pyrimidines / adverse effects*
  • Pyrimidines / therapeutic use

Substances

  • Antineoplastic Agents
  • Benzamides
  • Piperazines
  • Pyrimidines
  • Imatinib Mesylate
  • Protein-Tyrosine Kinases