Your browser doesn't support javascript.
loading
Potentially life­threatening severe cutaneous adverse reactions associated with tyrosine kinase inhibitors (Review).
Coleman, Emily L; Olamiju, Brianna; Leventhal, Jonathan S.
Affiliation
  • Coleman EL; Yale School of Medicine, New Haven, CT 06510, USA.
  • Olamiju B; Yale School of Medicine, New Haven, CT 06510, USA.
  • Leventhal JS; Yale School of Medicine, New Haven, CT 06510, USA.
Oncol Rep ; 45(3): 891-898, 2021 03.
Article in En | MEDLINE | ID: mdl-33650659
ABSTRACT
Tyrosine kinase inhibitors (TKIs) have emerged as a new frontier of cancer therapy. These agents include inhibitors of epidermal growth factor receptor (EGFR), human epidermal growth factor receptor 2 (HER2), BRAF, mitogen­activated protein kinase kinase (also referred to as MEK), bcr­abl, c­KIT, platelet­derived growth factor (PDGFR), fibroblast growth factor receptor (FGFR), anaplastic lymphoma kinase (ALK) and vascular endothelial growth factor (VEGF). Along with the evolving applications of TKIs, there has been an increased recognition of the breadth of potential cutaneous toxicities to these agents. In this review, we provide an overview of potentially life­threatening severe cutaneous adverse reactions (SCARs) that may occur during therapy with TKIs. These toxicities include Stevens­Johnson Syndrome (SJS), toxic epidermal necrolysis (TEN), drug reaction with eosinophilia and systemic symptoms (DRESS), and acute generalized exanthematous pustulosis (AGEP).
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein-Tyrosine Kinases / Drug Eruptions / Protein Kinase Inhibitors Type of study: Diagnostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Oncol Rep Journal subject: NEOPLASIAS Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Protein-Tyrosine Kinases / Drug Eruptions / Protein Kinase Inhibitors Type of study: Diagnostic_studies / Risk_factors_studies Limits: Humans Language: En Journal: Oncol Rep Journal subject: NEOPLASIAS Year: 2021 Document type: Article Affiliation country: