Condition: Non-small Cell Lung Cancer Stage III · Sponsor: Georgetown University
The goal of this clinical trial is to learn about neoadjuvant cemiplimab with histology-specific chemotherapy followed by resection and adjuvant cemiplimab in stage 3 non-small cell lung cancer (NSCLC) with contralateral mediastinal or ipsilateral supraclavicular lymph node (N3) involvement.. The main question it aims to answer is whether patients with stage 3 NSCLC with involvement of lymph nodes can undergo surgery to remove the cancer after receiving treatment with chemotherapy + immunotherapy. Participants will receive FDA-approved chemotherapy called platinum-doublet chemotherapy together with an immunotherapy drug targeting the immune marker PD-1 called cemiplimab. Patients will receive a 3 drug combination for 4 total treatments given every 3 weeks before surgery. After surgery, patients will have the option to undergo radiation therapy if it is recommended by their treatment team. After this, they will receive cemiplimab every 3 weeks for one year.
This description comes directly from the study's public registry record.
Joshua Reuss, MD · 202-444-2223 · Joshua.E.Reuss@gunet.georgetown.edu
Always discuss trial participation with your own doctor first.
| Lombardi Comprehensive Cancer Center, Georgetown University | Washington D.C., District of Columbia, United States | Recruiting |
| Washington University School of Medicine-Sitemen Cancer Center | St Louis, Missouri, United States | Recruiting |
| UVA Comprehensive Cancer Center | Charlottesville, Virginia, United States | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06449313