Jerry Hsu, Lena Dixit, Vishal Jhanji, Sumayya Ahmad
{"title":"角膜融化与癌症免疫治疗相关","authors":"Jerry Hsu, Lena Dixit, Vishal Jhanji, Sumayya Ahmad","doi":"10.1097/coa.0000000000000005","DOIUrl":null,"url":null,"abstract":"Purpose: The purpose of this study was to describe cases of corneal melt associated with systemic cancer immunotherapy. Methods: This is a case series of 6 patients. Results: Corneal melt was noted in all eyes, including 1 patient on an epidermal growth factor receptor (EGFR) inhibitor and another on a human epidermal growth factor 2 (HER2) inhibitor that resolved on serum tears; 1 patient on a fibroblast growth factor receptor (FGFR) inhibitor that stabilized on serum tears and amniotic membrane; 1 patient on a Bruton tyrosine kinase (BTK) inhibitor and another on a breakpoint cluster region protein-abelson murine leukemia viral oncogene homolog 1 (BCR-ABL) inhibitor that both had corneal thinning with perforation; and 1 patient with bilateral corneal thinning complicated by a fungal superinfection after long-term use of a programmed cell death protein 1 (PD-1) inhibitor. Conclusions: While primarily described with EGFR inhibitors, corneal melt may present with vision-threatening consequences in other classes of cancer immunotherapy including FGFR inhibitors, PD-1 inhibitors, and other tyrosine kinase inhibitors.","PeriodicalId":72708,"journal":{"name":"Cornea open","volume":"480 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Corneal Melt Associated With Cancer Immunotherapy\",\"authors\":\"Jerry Hsu, Lena Dixit, Vishal Jhanji, Sumayya Ahmad\",\"doi\":\"10.1097/coa.0000000000000005\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Purpose: The purpose of this study was to describe cases of corneal melt associated with systemic cancer immunotherapy. Methods: This is a case series of 6 patients. Results: Corneal melt was noted in all eyes, including 1 patient on an epidermal growth factor receptor (EGFR) inhibitor and another on a human epidermal growth factor 2 (HER2) inhibitor that resolved on serum tears; 1 patient on a fibroblast growth factor receptor (FGFR) inhibitor that stabilized on serum tears and amniotic membrane; 1 patient on a Bruton tyrosine kinase (BTK) inhibitor and another on a breakpoint cluster region protein-abelson murine leukemia viral oncogene homolog 1 (BCR-ABL) inhibitor that both had corneal thinning with perforation; and 1 patient with bilateral corneal thinning complicated by a fungal superinfection after long-term use of a programmed cell death protein 1 (PD-1) inhibitor. Conclusions: While primarily described with EGFR inhibitors, corneal melt may present with vision-threatening consequences in other classes of cancer immunotherapy including FGFR inhibitors, PD-1 inhibitors, and other tyrosine kinase inhibitors.\",\"PeriodicalId\":72708,\"journal\":{\"name\":\"Cornea open\",\"volume\":\"480 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-03-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cornea open\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1097/coa.0000000000000005\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cornea open","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1097/coa.0000000000000005","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Purpose: The purpose of this study was to describe cases of corneal melt associated with systemic cancer immunotherapy. Methods: This is a case series of 6 patients. Results: Corneal melt was noted in all eyes, including 1 patient on an epidermal growth factor receptor (EGFR) inhibitor and another on a human epidermal growth factor 2 (HER2) inhibitor that resolved on serum tears; 1 patient on a fibroblast growth factor receptor (FGFR) inhibitor that stabilized on serum tears and amniotic membrane; 1 patient on a Bruton tyrosine kinase (BTK) inhibitor and another on a breakpoint cluster region protein-abelson murine leukemia viral oncogene homolog 1 (BCR-ABL) inhibitor that both had corneal thinning with perforation; and 1 patient with bilateral corneal thinning complicated by a fungal superinfection after long-term use of a programmed cell death protein 1 (PD-1) inhibitor. Conclusions: While primarily described with EGFR inhibitors, corneal melt may present with vision-threatening consequences in other classes of cancer immunotherapy including FGFR inhibitors, PD-1 inhibitors, and other tyrosine kinase inhibitors.