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Clinical Trial Summary

This study is designed to identify the predictive biomarker for immunotherapy using patient samples (tumor tissue, blood, fecal material) who treated with immune checkpoint inhibitor.


Clinical Trial Description

[Sample acquisition]

- Informed consent is waived for those who agree to donate samples left over from other clinical trials or acquired for other purposes to be used for other research by the sign to master agreement in advance.

- The study will be conducted based on the purposes indicated in the master agreement signed by tissue donator [Clinical data acquisition]

- Baseline demographics: Sex, Birth date, expire date (last follow-up date for the survivals)

- Lung cancer treatment history: diagnosed date, treatment history (surgery, radiation therapy, chemotherapy, immunotherapy treatment history, and responses), general performance, metastatic sites

- Lung cancer histologic information: pathology, histologic subtype, EGFR mutation profile, ALK-rearrangement result ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03578185
Study type Observational
Source Samsung Medical Center
Contact Se-hoon Lee, MD
Phone +82-10-4759-7640
Email sehoon.lee@samsung.com
Status Recruiting
Phase
Start date April 11, 2018
Completion date December 31, 2020

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