About this trial
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.
Eligibility criteria
Qualifiers
Age ≥ 18 years at time of signing the informed consent form (ICF).
Histologically or cytologically confirmed stage 3 B/C Non-Small Cell Lung Cancer (NSCLC) as assessed per the 8th American Joint Committee on Cancer (AJCC) with pathologically-confirmed contralateral mediastinal or ipsilateral supraclavicular (N3) lymph node involvement.
Primary tumor appropriate for resection with curative intent as assessed by the treating surgeon prior to study enrollment.
Absence of major associated pathologies and co-morbidities that elevate surgery risk to a prohibitive level, as assessed by treating surgeon prior to study enrollment.
Disqualifiers
NSCLC with histology containing any of the following: large cell neuroendocrine carcinoma, small cell lung cancer.
Primary tumor not deemed appropriate for surgical resection as assessed by treating surgeon.
Tumor with direct invasion of: mediastinum, diaphragm, heart, great vessels, trachea, esophagus, vertebral body, or carina.
Any other tumor characteristic making it not suitable for resection as determined by treating surgeon.
Trial design
Treatments tested in this trial
- Cemiplimab-Rwlc
Treatment groups
Sponsors and collaborators
Georgetown University
Lead sponsor
Regeneron Pharmaceuticals
Collaborator