Related Experiment Video
Updated: Mar 8, 2026

Testing Targeted Therapies in Cancer using Structural DNA Alteration Analysis and Patient-Derived Xenografts
Published on: July 25, 2020
Tissue is the issue and tissue competition. Re-biopsy for mutation T790: where and why?
Paul Zarogoulidis1, Mina Gaga2, Haidong Huang3
1Pulmonary Department-Oncology Unit, ``G. Papanikolaou`` General Hospital, Aristotle University of Thessaloniki, Thessaloniki, Greece. pzarog@hotmail.com.
Abstract:
Lung cancer is still the leading cause of death among all cancers. During the last 15 years, pharmacogenomics of lung cancer have established targeted therapy with tyrosine kinase inhibitors (TKIs) for epidermal growth factor receptor (EGFR) positive patients in adenocarcinoma or mixed adenosquamus lung cancer patients. However; while novel drugs are released in the market, at the same time novel mutations are observed after tyrosine kinase inhibitor administration. Recently the novel mutation T790 was observed and is highly prevalent in patients already treated with a TKI. A new drug targeting this mutation is already on the market, however; the most important factor for successful treatment in these patients, is adequate tissue re-sampling so that novel mutations can be detected.
Insights
Lung cancer treatment advances with targeted therapies like tyrosine kinase inhibitors (TKIs) for EGFR-positive patients. Detecting new mutations, such as T790, through adequate tissue re-sampling is crucial for successful treatment.
Area of Science:
- Oncology
- Pharmacogenomics
- Molecular Biology
Background:
- Lung cancer remains a leading cause of cancer-related mortality worldwide.
- Pharmacogenomics has enabled targeted therapies, specifically tyrosine kinase inhibitors (TKIs), for patients with epidermal growth factor receptor (EGFR) mutations in lung adenocarcinoma.
- The emergence of novel mutations after TKI treatment presents a significant clinical challenge.
More Related Videos
11:20Simple and Rapid Method to Obtain High-quality Tumor DNA from Clinical-pathological Specimens Using Touch Imprint Cytology
Published on: March 21, 2018
13:24Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
Published on: April 11, 2016