Registry Measuring the Impact of Adding RNA Expression Testing on Referral Decisions in Early Stage Lung Cancer Patients and Assessing the Disease-free Survival With Long-term Follow-up
Status: | Recruiting |
---|---|
Conditions: | Lung Cancer, Cancer |
Therapuetic Areas: | Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 4/21/2016 |
Start Date: | May 2014 |
End Date: | December 2018 |
Contact: | Kristen Rushton |
Email: | krushton@myriad.com |
LUNG CAncerREgistry: An Open Registry to Measure the Impact of Adding RNA Expression Testing (myPlan Lung Cancer) on Referral Decisions and to Assess Disease-free Survival With Long-term Follow-up in Newly Diagnosed Early Stage Lung Adenocarcinoma Patients
This registry is intended to measure the effect of myPlan Lung Cancer™ test has on treatment
decisions of Surgeons when added to standard clinical-pathological parameters in patients
with early stage NSCLC.The sponsor is conducting two parallel registries, with one directed
at Surgeons (ONC003) and the other at Oncologists (ONC006).This registry is specific to
Surgeons (ONC003). Outcomes measures on lung cancer relapse and death from any cause will be
collected.
decisions of Surgeons when added to standard clinical-pathological parameters in patients
with early stage NSCLC.The sponsor is conducting two parallel registries, with one directed
at Surgeons (ONC003) and the other at Oncologists (ONC006).This registry is specific to
Surgeons (ONC003). Outcomes measures on lung cancer relapse and death from any cause will be
collected.
Inclusion Criteria:
- Diagnosis of early stage non-small cell lung adenocarcinoma
- Sub-population staging (IA, IB or IIA) as judged by the standard of practice at the
investigational site
- Resection of tumor within previous 2 months of enrollment
- ECOG performance of 0-2
- A minimum life expectancy of six months
Exclusion Criteria:
- Pre-operative radiation or chemotherapy for NSCLC
- Post-operative radiation or chemotherapy for NSCLC
- Enrollment in a separate clinical trial restricting treatment options
- Unable to provide informed consent
We found this trial at
1
site
Seattle, Washington 98105
Principal Investigator: Vallieres
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