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

成纤维细胞生长因子受体 医学 成纤维细胞生长因子受体1 癌症研究 酪氨酸激酶 生长因子受体 成纤维细胞生长因子受体2 成纤维细胞生长因子 受体酪氨酸激酶 成纤维细胞生长因子23 内科学 受体 甲状旁腺激素
作者
M. Teresa Magone,Iris R. Hartley,Edmond J. FitzGibbon,Rachel Bishop,Mike Arango,Susan Moran,Roo Vold,Jaydira Del Rivero,Karen Pozo,Jamie Streit,Kelly L. Roszko,Michael T. Collins,Rachel I. Gafni
出处
期刊:Ophthalmology [Elsevier BV]
卷期号:128 (4): 624-626 被引量:12
标识
DOI:10.1016/j.ophtha.2020.08.026
摘要

Fibroblast growth factor receptors (FGFRs) are expressed in all major organs, including the eye (Fig S1, available at www.aaojournal.org). 1 Chae Y.K. Ranganath K. Hammerman P.S. et al. Inhibition of the fibroblast growth factor receptor (FGFR) pathway: the current landscape and barriers to clinical application. Oncotarget. 2017; 8: 16052-16074 Crossref PubMed Scopus (183) Google Scholar Fibroblast growth factor receptor tyrosine kinase inhibitors (TKIs) are under investigation, targeting various cancer types. 1 Chae Y.K. Ranganath K. Hammerman P.S. et al. Inhibition of the fibroblast growth factor receptor (FGFR) pathway: the current landscape and barriers to clinical application. Oncotarget. 2017; 8: 16052-16074 Crossref PubMed Scopus (183) Google Scholar Furthermore, 2 FGFR-TKIs have recently been Food and Drug Administration-approved for treating advanced urothelial carcinoma and cholangiocarcinoma. Fibroblast growth factor receptor inhibition commonly leads to hyperphosphatemia, fatigue, stomatitis, alopecia, nail changes, dry eye, and blurred vision. 2 Javle M. Lowery M. Shroff R.T. et al. Phase II study of BGJ398 in patients with FGFR-altered advanced cholangiocarcinoma. J Clin Oncol. 2018; 36: 276-282 Crossref PubMed Scopus (300) Google Scholar Re: Magone et al.: Ocular adverse effects of infigratinib, a new fibroblast growth factor receptor tyrosine kinase inhibitor (Ophthalmology. 2021;128:624–626)OphthalmologyVol. 128Issue 9PreviewWe read the article by Magone et al.1 The authors provide a useful description of the anterior segment findings in a small cohort of patients. However, we suspect there may be a discrepancy in their description of the posterior segment findings of one patient. They state that “None of the patients developed retinal pathology, including patient number 5, who had a history of reversible ingrafitinib-related bilateral retinal pigment epithelium detachments.” Although no longer present, we feel it important to comprehend this fundus abnormality fully. Full-Text PDF

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