CTRI/2018/08/015290
Completed
未知
An observational, multicentre, Prospective study to evaluate concordance of detecting EGFR mutation by circulating tumour free DNA versus tissues biopsy in NSCLC (CONCORDANCE) - CONCORDANCE
Overview
- Phase
- 未知
- Status
- Completed
- Sponsor
- AstraZeneca Pharma India Ltd
- Enrollment
- 245
Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Observational
Eligibility Criteria
Inclusion Criteria
- •1\. Patients who provide written informed consent
- •2\. Patients aged 18 years and older
- •3\. Newly diagnosed patients with Metastatic (stage IV) NSCLC.
- •4\. Histologically confirmed Adenocarcinoma NSCLC patients as per tissue biopsy and the sample sent for EGFR mutation analysis.
- •5\. Patient should be naïve for any systemic treatment (i.e. no chemotherapy or EGFR\-TKI)
- •6\. Provision of a routine blood (plasma) sample
- •The prescription of any medicinal product is clearly separated from the decision to include the subject in the study.
Exclusion Criteria
- •1\. Patient with any medical condition that, in the opinion of the investigator, would interfere with outcome of the study
- •2\. Patient participating in any other interventional clinical study/trial.
Investigators
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