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Ocular toxicity associated with high-dose carmustine

B J Shingleton, D C Bienfang, D M Albert

    Archives of Ophthalmology (Chicago, Ill. : 1960)
    |November 1, 1982
    PubMed
    Summary
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    Carmustine, a nitrosourea, can cause delayed ocular toxicity in patients undergoing high-dose chemotherapy. This includes vision loss and retinal changes, particularly with intra-arterial administration.

    Area of Science:

    • Ophthalmology
    • Oncology
    • Pharmacology

    Background:

    • Carmustine (BCNU) is a nitrosourea chemotherapy agent.
    • Ocular side effects of carmustine are not well-established.
    • High-dose carmustine is used with autologous bone marrow rescue.

    Observation:

    • Delayed bilateral ocular toxicity occurred in 2/50 patients receiving high-dose intravenous carmustine.
    • Delayed ocular toxicity occurred ipsilaterally in 7/10 patients receiving intra-arterial carotid carmustine.
    • Ocular toxicity symptoms appeared 4 weeks post-IV and 2-14 weeks post-intra-arterial treatment.

    Findings:

    • Funduscopic findings included arterial narrowing, nerve fiber-layer infarcts, and intraretinal hemorrhages.
    • Fluorescein angiography showed perivascular staining, capillary leakage, and optic disc hyperfluorescence.

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  • One patient experienced cilioretinal artery occlusion and choroidal fibrin thrombi.
  • Implications:

    • High-dose carmustine, especially via intra-arterial route, poses a risk of significant ocular toxicity.
    • Ocular toxicity can manifest as severe vision loss.
    • Further research is needed to understand and mitigate carmustine-induced ocular complications.