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Published on: August 11, 2017
Relationship of thyroid transcription factor 1 to EGFR status in non-small-cell lung cancer
B S Sheffield1, I E Bosdet1, R H Ali2
1Department of Pathology and Laboratory Medicine, BC Cancer Agency. Vancouver, BC.
Background:
Activating mutations of the epidermal growth factor receptor (EGFR) gene are known to drive a proportion of non-small-cell lung cancers. Identification of lung cancers harbouring such mutations can lead to effective treatment using one of the agents that targets and blocks egfr-mediated signalling.
Methods:
All specimens received at the BC Cancer Agency (Vancouver) for EGFR testing were prospectively identified and catalogued, together with clinical information and EGFR status, over a 14-month period.
Results:
Specimens from 586 patients were received for EGFR testing, and EGFR status was reported for 509 patients. No relationship between specimen type or site of origin and EGFR test failure rate was identified. Concurrent immunohistochemical (ihc) status for thyroid transcription factor 1 (ttf1) was available for 309 patients. The negative predictive value of ttf1-negative status by ihc was 94.2% for predicting negative EGFR status.
Conclusions:
In patients with limited tissue available for testing, a surrogate for EGFR status would aid in timely management. Immunohistochemistry for ttf1 is readily available and correlates highly with EGFR status. In conjunction with genetic assays, ttf1 could be used to optimize an EGFR testing strategy.
Insights
Thyroid transcription factor 1 (TTF1) immunohistochemistry can predict epidermal growth factor receptor (EGFR) status in non-small-cell lung cancer. TTF1 negativity by IHC is highly predictive of negative EGFR status, aiding treatment decisions.
Area of Science:
- Oncology
- Molecular Diagnostics
- Cancer Biomarkers
Background:
- Activating mutations in the epidermal growth factor receptor (EGFR) gene drive a subset of non-small-cell lung cancers (NSCLC).
- Identifying EGFR mutations in NSCLC patients enables targeted therapy with EGFR-blocking agents.
- Accurate EGFR mutation status is crucial for effective NSCLC treatment strategies.
Purpose of the Study:
- To evaluate the utility of thyroid transcription factor 1 (TTF1) immunohistochemistry (IHC) as a surrogate marker for EGFR mutation status in NSCLC.
- To determine if TTF1 IHC can aid in optimizing EGFR testing strategies, especially in cases with limited tissue.
- To assess the correlation between TTF1 negativity and EGFR mutation status in a clinical setting.
Main Methods:
- Prospective collection and cataloging of all specimens submitted for EGFR testing at BC Cancer Agency over 14 months.
- Analysis of EGFR test results and associated clinical information.
- Concurrent immunohistochemical (IHC) analysis for TTF1 on available specimens.
Main Results:
- EGFR status was reported for 509 out of 586 patient specimens received for testing.
- No significant relationship was found between specimen type/origin and EGFR test failure rates.
- TTF1-negative status by IHC demonstrated a high negative predictive value (94.2%) for predicting negative EGFR status.
Conclusions:
- Immunohistochemistry for TTF1 is a readily available and reliable surrogate marker for EGFR status in NSCLC.
- TTF1 IHC can help optimize EGFR testing strategies, particularly when tissue is limited, facilitating timely patient management.
- Combining TTF1 IHC with genetic assays can enhance the efficiency of EGFR testing in NSCLC.
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