Abstract
Epidermal growth factor receptor (EGFR) mutation analysis is recommended for lung cancer patients prior to the prescription of first-line EGFR tyrosine kinase inhibitors in order to predict response to treatment. There are many methods available to identify mutations in the EGFR gene; a large number of clinical laboratories use the therascreen EGFR RGQ PCR kit (Qiagen). We report a case where this kit detected an exon 19 deletion, predicting sensitivity to tyrosine kinase inhibitors (TKIs), which on further analysis was found to be a 2?bp indel (c.2239_2240delinsCC, p.(Leu747Pro)). Two of four published cases with this mutation were found to be associated with resistance to EGFR TKI. The sample was also tested using two other commercial kits, one of which indicated a deletion. This is a rare mutation making the erroneous detection of a deletion unlikely; however, it is important that clinical laboratories are aware of the potential failings of two commercial kits for EGFR mutation analysis.
| Original language | English |
|---|---|
| Pages (from-to) | 734-735 |
| Number of pages | 2 |
| Journal | Journal of Clinical Pathology |
| Volume | 67 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - Aug 2014 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Adenocarcinoma
- Antineoplastic Agents
- DNA Mutational Analysis
- Humans
- Lung Neoplasms
- Protein Kinase Inhibitors
- Receptor, Epidermal Growth Factor
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