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Clinical Trial
. 2021 Apr;128(4):624-626.
doi: 10.1016/j.ophtha.2020.08.026. Epub 2020 Sep 1.

Ocular Adverse Effects of Infigratinib, a New Fibroblast Growth Factor Receptor Tyrosine Kinase Inhibitor

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Clinical Trial

Ocular Adverse Effects of Infigratinib, a New Fibroblast Growth Factor Receptor Tyrosine Kinase Inhibitor

M Teresa Magone et al. Ophthalmology. 2021 Apr.
No abstract available

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Figures

Figure 2.
Figure 2.
A, Photograph of the right cornea of patient number 4 showing basement membrane haze grade 1 (white arrows) localized to the anterior Basement membrane (BM) (inset) with clear stroma underneath. The patient also had mild punctate keratopathy (center) and deep epitheliopathy with a demarcation line (black horizontal arrow), which appeared 87 days after starting infigratinib and only resolved after discontinuation of the study drug as seen in B. B, Same eye of patient number 4 at 1 month after discontinuation of infigratinib. The demarcation line resolved, but permanent nasal anterior basement membrane haze remained (arrow). C, Photograph of cornea of patient number 1 showing small areas of opacification (arrows main photograph) localized to the deep corneal stroma and Descemets membrane (DM) on cross-beam view (left inset white arrows) and high-resolution OCT (right inset white arrows). The patient did not have overlying corneal edema or anterior chamber inflammation. This grade 2 keratitis adverse event (AE) occurred 64 days after starting infigratinib and led to drug interruption. D, Photograph of cornea of patient number 1 on study day 140 showing grade 2 symptomatic infigratinib-related epitheliopathy causing blurry vision. Symptomatic epitheliopathy occurred on average 91 ± 53 days (mean ± standard deviation) after starting infigratinib in patients with healthy baseline examination results.

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References

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