A new medical therapy for Cushing disease?
other · Level V
Where this comes from
- Record sourced from PubMed, PMID 22105164.
- Also identified by DOI 10.1172/JCI61127 and PMC identifier 3226342.
- No licence information is recorded for this record.
- Because redistribution is not established, this page shows the abstract only. Follow the links below for the full text.
Abstract
Members of the ErbB family of cell surface tyrosine kinase receptors are important targets for cancer treatment because they frequently contribute to the pathogenesis of malignancy. In this issue of the JCI, Fukuoka et al. generate data that suggest that using a tyrosine kinase inhibitor (TKI) against epidermal growth factor receptor (EGFR; also known as ErbB1) may be a novel approach for treating patients with hypercortisolemia due to pituitary corticotroph adenomas (Cushing disease). While surgical resection remains the cornerstone of treatment for individuals with such tumors, this study suggests that TKIs could perhaps be used to reduce tumor size prior to surgery or to treat recurrent disease after surgery.
Medical subject headings
- ACTH-Secreting Pituitary Adenoma
- Adenoma
- ErbB Receptors
- Molecular Targeted Therapy
- Protein Kinase Inhibitors
- Quinazolines