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40 trials tracked for Non-Small Cell Lung Cancer (NSCLC): 13 in phase 3 or 4 and 8 with published results. The most-cited published study has 6553 citations.
Showing the 40 most-cited and recently-updated of 40 trials. Browse the full registry →
Trial data sourced from ClinicalTrials.gov. Counts describe the research landscape and are not a treatment recommendation. Informational only — not medical advice.
Several immunotherapies have demonstrated clinical activity in NSCLC. Pembrolizumab showed significant improvements in both overall survival (OS) and progression-free survival (PFS) 7, with a high rate of adverse events reported across study arms 7. In other trials, Nivolumab was evaluated for safety and efficacy; while specific grade 3-5 treatment-related adverse events were recorded 8, the drug also showed consistent results in large-scale assessments regarding progression-free survival 11. Durvalumab demonstrated a measurable percentage of patients remaining progression-free at 12 months 22 and was evaluated for safety profiles involving high-grade treatment-related adverse events [20, 22].
Atezolizumab showed no statistically significant difference in PFS in the PD-L1 positive analysis set or the full analysis set 1. Tiragolumab demonstrated a statistically significant improvement in investigator-assessed PFS specifically in patients with PD-L1 expression at TPS/TC >=1% 2, though it did not reach significance in other primary endpoints like OS 2. Other targeted therapies included Crizotinib, which showed a significant improvement in PFS and objective response rate (ORR) compared to the control arm, despite no significant difference in overall survival 9.
Combination therapies also provided evidence for NSCLC management. The combination of cetuximab with cisplatin and vinorelbine significantly improved both OS and best overall response rate 14, whereas the addition of cetuximab to a platinum-based doublet chemotherapy did not show statistically significant improvements in OS or time to treatment failure 13. Other established agents include Osimertinib 4, Nivolumab 5, Gefitinib 6, and Eribulin, though the latter did not reach statistical significance for OS, PFS, or ORR 12.
AI synthesis of 15 cited trials, updated Jul 30, 2026. Informational only — not medical advice; trial data sourced from ClinicalTrials.gov. How we use AI.