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Clinical Trial Summary

This study is a prospective cohort study to evaluate the peripheral blood lymphocyte subsets as predicative biomarkers reflecting the efficacy and toxicity in patients with locally advanced non-small cell lung cancer (NSCLC) received chemoradiotherapy (CRT) with or without immune checkpoint inhibitors (ICIs).


Clinical Trial Description

All patients had a pathologically confirmed locally advanced NSCLC according to the 8th AJCC staging system and received definitive radiotherapy, concurrently or sequentially combined with platinum-based doublet chemotherapy. The peripheral blood samples at various time points including before radiation, 4 weeks after beginning of radiation, the end of radiation, 1 month post radiation, and 1 month post consolidation immunotherapy were collected for lymphocyte subsets detection. The subjects will be divided into two groups according to whether patients received ICIs, namely, NSCLC patients received CRT plus ICIs and NSCLC patients received CRT. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06287320
Study type Observational
Source Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Contact Nan Bi, MD
Phone 8601087788799
Email binan_email@163.com
Status Recruiting
Phase
Start date March 1, 2024
Completion date February 28, 2026

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