Identifier | Trials | Phase | Indication | Population | Intervention | mORR | mPFS | 1-year PFS rate | mOS | 1-year OS rate | Any cause of AE rates ≥grade 3 |
---|---|---|---|---|---|---|---|---|---|---|---|
NCT02578680 | Keynote-189 | III | First-line | Treatment-naive metastatic non-squamous NSCLC without EGFR/ALK alteration | Platinum-based CT | 18.9% | 4.9 months | 17.3% | 11.3 months | 49.4% | 65.8% |
Platinum-based CT plus pembrolizumab | 47.6% | 8.8 months | 34.1% | NR | 69.2% | 67.2% | |||||
NCT02775435 | Keynote-407 | III | First-line | Untreated metastatic squamous NSCLC without EGFR/ALK alteration | Carboplatin-based CT | 38.4% | 4.8 months | NA | 11.3 months | 48.3% | 68.2% |
Carboplatin-based CT plus pembrolizumab | 57.9% | 6.4 months | NA | 15.9 months | 65.2% | 69.8% | |||||
NCT02477826 | Checkmate-227 | III | First-line | Untreated recurrent NSCLC of high mutation burden without EGFR/ALK alteration | Platinum-based CT | 26.9% | 5.5 months | 13.2% | NA | NA | 36.0%* |
Nivolumab plus Ipilimumab | 45.3% | 7.2 months | 42.6% | NA | NA | 37.0%* | |||||
NCT02366143 | IMpower150 | III | First-line | Untreated metastatic non-squamous NSCLC (wild type group) | Bevacizumab plus carboplatin plus paclitaxel (BCP) | 48.0% | 6.8 months | 18.0% | 14.7 months# | 60.6%# | 50.0%+ |
Atezolizumab plus BCP | 63.5% | 8.3 months | 36.5% | 19.2 months# | 67.3%# | 58.5%+ | |||||
NCT02657434 | IMpower131 | III | First-line | Untreated metastatic squamous cell NSCLC without EGFR/ALK alteration | Carboplatin-based CT | 41.0% | 5.6 months | 12.0% | 13.9 months# | 56.9%# | 58.0%* |
Carboplatin-based CT plus atezolizumab | 49.0% | 6.3 months | 24.7% | 14.0 months# | 55.6%# | 69.0%* | |||||
NCT02657434 | IMpower132 | III | First-line | Untreated metastatic non-squamous NSCLC without EGFR/ALK alteration | Platinum-based CT | 32.0% | 5.2 months | 17.0% | 13.6 months# | 55.4%# | 59.0% |
Platinum-based CT plus atezolizumab | 47.0% | 7.6 months | 33.7% | 18.1 months# | 59.6%# | 69.0% |