Title |
Osimertinib making a breakthrough in lung cancer targeted therapy
|
---|---|
Published in |
OncoTargets and therapy, September 2016
|
DOI | 10.2147/ott.s114722 |
Pubmed ID | |
Authors |
Haijun Zhang |
Abstract |
Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are the evidence-based first-line treatment for advanced non-small-cell lung cancer that harbors sensitizing EGFR mutations (EGFRm(+)) such as exon 19 deletions and L858R substitutions in exon 21. However, acquired resistance to EGFR TKIs is mostly driven by a second-site EGFR T790M mutation, which negates their inhibitory activity. Osimertinib (AZD9291, Tagrisso™), an oral, third-generation EGFR TKI, has been designed to target the EGFR T790M mutation, while sparing wild-type EGFR. In this up-to-date review, focus is not only on the structure, mechanisms, and pharmacokinetics of osimertinib but also on summarizing clinical trials and making recommendations of osimertinib for patients with non-small-cell lung cancer. |
X Demographics
Geographical breakdown
Country | Count | As % |
---|---|---|
India | 1 | 33% |
Unknown | 2 | 67% |
Demographic breakdown
Type | Count | As % |
---|---|---|
Members of the public | 3 | 100% |
Mendeley readers
Geographical breakdown
Country | Count | As % |
---|---|---|
Korea, Republic of | 1 | <1% |
Unknown | 101 | 99% |
Demographic breakdown
Readers by professional status | Count | As % |
---|---|---|
Student > Bachelor | 19 | 19% |
Student > Master | 15 | 15% |
Student > Ph. D. Student | 11 | 11% |
Researcher | 8 | 8% |
Student > Doctoral Student | 6 | 6% |
Other | 11 | 11% |
Unknown | 32 | 31% |
Readers by discipline | Count | As % |
---|---|---|
Biochemistry, Genetics and Molecular Biology | 15 | 15% |
Medicine and Dentistry | 15 | 15% |
Pharmacology, Toxicology and Pharmaceutical Science | 12 | 12% |
Agricultural and Biological Sciences | 11 | 11% |
Chemistry | 11 | 11% |
Other | 6 | 6% |
Unknown | 32 | 31% |