{"title":"肺癌发生阿法替尼相关皮肤反应","authors":"E. Karaman, A. Ulaş, Ayça ADIACAR SEZER","doi":"10.37047/jos.2022-92025","DOIUrl":null,"url":null,"abstract":"ABS TRACT Afatinib is an irreversible second-generation tyrosine kinase inhibitor. It is used to treat epidermal growth factor receptor (EGFR) mutation-positive lung adenocarcinoma. The most well-known side effects associated with afatinib are diarrhea, rashes or acne and stomatitis. Herein, we present a case of skin toxicity that developed in the late phase of afatinib treatment. A 51-year-old, non-smoker woman diagnosed with EGFR deletion-19 mutant advanced lung adenocarcinoma. Afatinib was initiated as the first-line treatment. At the twelfth treatment month, Grade-2 acneiform dermatitis, paronychia, and hand-foot syndrome developed. Despite the interruption or discontinuation of afatinib treatment and local/systemic steroid treatments, the lesions did not regress. The patient was responsive to afatinib; however, the treatment was discontinued in the eighteenth month of treatment. The treatment response may be predicted by the severity of skin toxicities owing to afa-tinib. They occur in the early treatment phase and are commonly observed at the Grade 1-2 level.","PeriodicalId":31838,"journal":{"name":"Journal of Oncological Sciences","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Lung Carcinoma Developing Afatinib-Associated Skin Reactions\",\"authors\":\"E. Karaman, A. Ulaş, Ayça ADIACAR SEZER\",\"doi\":\"10.37047/jos.2022-92025\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"ABS TRACT Afatinib is an irreversible second-generation tyrosine kinase inhibitor. It is used to treat epidermal growth factor receptor (EGFR) mutation-positive lung adenocarcinoma. The most well-known side effects associated with afatinib are diarrhea, rashes or acne and stomatitis. Herein, we present a case of skin toxicity that developed in the late phase of afatinib treatment. A 51-year-old, non-smoker woman diagnosed with EGFR deletion-19 mutant advanced lung adenocarcinoma. Afatinib was initiated as the first-line treatment. At the twelfth treatment month, Grade-2 acneiform dermatitis, paronychia, and hand-foot syndrome developed. Despite the interruption or discontinuation of afatinib treatment and local/systemic steroid treatments, the lesions did not regress. The patient was responsive to afatinib; however, the treatment was discontinued in the eighteenth month of treatment. The treatment response may be predicted by the severity of skin toxicities owing to afa-tinib. They occur in the early treatment phase and are commonly observed at the Grade 1-2 level.\",\"PeriodicalId\":31838,\"journal\":{\"name\":\"Journal of Oncological Sciences\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Oncological Sciences\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.37047/jos.2022-92025\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Oncological Sciences","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.37047/jos.2022-92025","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
ABS TRACT Afatinib is an irreversible second-generation tyrosine kinase inhibitor. It is used to treat epidermal growth factor receptor (EGFR) mutation-positive lung adenocarcinoma. The most well-known side effects associated with afatinib are diarrhea, rashes or acne and stomatitis. Herein, we present a case of skin toxicity that developed in the late phase of afatinib treatment. A 51-year-old, non-smoker woman diagnosed with EGFR deletion-19 mutant advanced lung adenocarcinoma. Afatinib was initiated as the first-line treatment. At the twelfth treatment month, Grade-2 acneiform dermatitis, paronychia, and hand-foot syndrome developed. Despite the interruption or discontinuation of afatinib treatment and local/systemic steroid treatments, the lesions did not regress. The patient was responsive to afatinib; however, the treatment was discontinued in the eighteenth month of treatment. The treatment response may be predicted by the severity of skin toxicities owing to afa-tinib. They occur in the early treatment phase and are commonly observed at the Grade 1-2 level.