{"title":"Accelerated Onset of Liver Failure after Prolonged Adjuvant Tamoxifen Use in Breast Cancer Patients","authors":"H. Heers, L. Mina, S. Bahadur, S. Lim","doi":"10.31487/j.cor.2020.04.11","DOIUrl":null,"url":null,"abstract":"Use of adjuvant endocrine therapy for women with hormone-receptor (HR)-positive breast cancer has\nbecome the standard of care. Tamoxifen, an orally available selective estrogen receptor modulator (SERM),\nis a commonly used endocrine therapy agent currently recommended for use in pre- or post-menopausal\nwomen with HR-positive breast cancer. Current evidence suggests that prolonged tamoxifen use may be\nimplicated in causing hepatotoxicity which may manifest as non-alcoholic steatohepatitis (NASH),\ncholestasis, cirrhosis, or hepatic necrosis. We herein present two cases of suspected tamoxifen-induced\nNASH resulting in fulminant liver failure. We also discuss literature surrounding tamoxifen-related\nhepatoxicity and implications in clinical practice.","PeriodicalId":10487,"journal":{"name":"Clinical Oncology and Research","volume":"10 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical Oncology and Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31487/j.cor.2020.04.11","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Use of adjuvant endocrine therapy for women with hormone-receptor (HR)-positive breast cancer has
become the standard of care. Tamoxifen, an orally available selective estrogen receptor modulator (SERM),
is a commonly used endocrine therapy agent currently recommended for use in pre- or post-menopausal
women with HR-positive breast cancer. Current evidence suggests that prolonged tamoxifen use may be
implicated in causing hepatotoxicity which may manifest as non-alcoholic steatohepatitis (NASH),
cholestasis, cirrhosis, or hepatic necrosis. We herein present two cases of suspected tamoxifen-induced
NASH resulting in fulminant liver failure. We also discuss literature surrounding tamoxifen-related
hepatoxicity and implications in clinical practice.