Non Small Cell Lung Cancer Patients Treated With Erlotinib Six Months or Longer
Completed
Conditions studied: Non Small Cell Lung Cancer
In brief
With roughly 80% of cancer patients receiving their oncology care in the community setting, the investigators are proposing to sample from a community-based center to evaluate the percentage of epidermal growth factor receptor (EGFR)-wild type patients that gain benefit from erlotinib and assess the clinical characteristics that are associated with erlotinib-responders. Additionally, biopsy specimens from enrolled patient cases that are EGFR-wt will be evaluated via exploratory genetic analysis for correlated markers.
Key facts
- Study ID
- NCT01522833
- Run by
- SCRI Development Innovations, LLC
- People needed
- 27
- Starts
- 2012-10-01
- Expected to finish
- 2015-02-01
- Last updated by the study team
- 2016-03-07
Who can join
Age: any. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients must have had NSCLC.
- Patients must have received erlotinib (single-agent) for six months or longer for NSCLC in the second/third line setting or as maintenance therapy.
- Patients must have tissue available for EGFR-mutation status testing (if not previously performed) or EGFR-mutation status test results available.
- Patients must have tissue available for exploratory genetic analysis.
- Patients must have all clinical information, treatment response data and outcomes data available for review.
- Patients must be deceased.
Where it is running
- Tennessee Oncology, PLLC — Nashville, Tennessee, United States
Full record on ClinicalTrials.gov
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