Evaluating the Implementation and Effectiveness of the Pink and Pearl Campaign on Lung Cancer Screening at Christian Hospital
NCT07146568
Cancer of the Lung, Lung Cancer
St Louis, Missouri, United States
View Trial DetailsNCT Number: NCT03578185
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.
Interested in participating?
Request Info18 year and older
All sexes
Observational
Samsung Medical Center, Seoul, Gangnam-gu, South Korea
[Sample acquisition]
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exculsion Criteria:
NA
Time frame: Baseline
Neoantigen, tumor mutation burden, MHC compatibility, T-cell receptor and associated immune gene signature (IFN-r, interferons such as IL-2 and interleukin family), T-cell subset (T cell surface marker such as CD4+, CD7+, CD8+, CD16, CD34+, CD38+, CD56+, etc.), PD-1/PD-L1 expression, etc.
Contact information is provided by the study sponsor or research team.
Jinhee Seo
CONTACT
Se-hoon Lee, MD
CONTACT
Samsung Medical Center
Other
Acronym: LC_Biomarker
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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