About this trial
Neoadjuvant immunotherapy followed by surgery has emerged as the standard treatment for locally advanced and resectable non-small cell lung cancer (NSCLC). However, conventional chemotherapy components may increase treatment-related toxicity, particularly in elderly populations. Additionally, the efficacy of preoperative immunochemotherapy for patients with PD-L1 expression \<1% remains to be improved. Emerging evidence has demonstrated that the combination of nivolumab (anti-PD-1) and ipilimumab (anti-CTLA-4) provides superior responses in the treatment of advanced NSCLC. However, the safety and efficacy of this strategy in the neoadjuvant setting remain controversial. Therefore, this single-arm clinical trial aims to evaluate the safety and feasibility of neoadjuvant nivolumab plus ipilimumab followed by surgery in treating locally advanced and resectable NSCLC.
Eligibility criteria
Qualifiers
Informed consent must be signed.
At least 18 years of age.
Histologically or cytologically confirmed non-small cell lung cancer (without EGFR, ALK mutation).
Have measurable and clinical stage II-IIIA with no known PD-L1 expression or PD-L1 ≤ 1%.
Disqualifiers
Patients with active autoimmune disease or history of autoimmune disease.
Patients have received other treatment for non-small cell lung cancer or for any other malignancy.
History of allergy to study drug components.
Pregnant or breast-feeding.
Trial design
Treatments tested in this trial
- Nivolumab & Ipilimumab