Table 2.
Phase 3 clinical trials that includes Immunotherapy for NSCLC in the first line.
Pathology | PDL-1 | Arm I (OS) | Arm II (OS) | HR | |
---|---|---|---|---|---|
KEYNOTE-024 | squamous (18%) and nonsquamous (82%) | ≥50% | Pembrolizumab | Investigator’s choice of platinum-based chemotherapy | |
30 months | 14.2 months | 0.63 | |||
KEYNOTE-042 | squamous (38%) and nonsquamous (62%) | ≥1% | Pembrolizumab | Investigator’s choice of platinum-based chemotherapy doublet | |
16.7 months | 12.1 months | 0.81 | |||
KEYNOTE-189 | nonsquamous | Any level | Pembrolizumab & Pemetrexed + Cisplatin/Carboplatin |
Pemetrexed + Cisplatin/Carboplatin | |
22 months | 10.7 month | 0.56 | |||
KEYNOTE-407 | squamous | Any level | Pembrolizumab & Carboplatin + paclitaxel or nab–paclitaxel |
Carboplatin + paclitaxel or nab–paclitaxel | |
15.9 months | 11.3 months | 0.64 | |||
CHECKMATE-227 | squamous (28%) and nonsquamous (72%) | Any level ≥1% <1% |
Nivolumab and Ipilimumab | Cisplatin/Carboplatin + Gemcitabine (for squamous) or pemetrexed (nonsquamous) |
|
17.1 months | 14.9 months | 0.79 | |||
17.2 months | 12.2 months | 0.62 | |||
CHECKMATE 9LA | squamous and nonsquamous | Any level | Nivolumab & Ipilimumab + Cisplatin/Carboplatin + Pemetrexed/Paclitaxel |
Cisplatin/Carboplatin + Pemetrexed/Paclitaxel |
|
15.6 months | 10.9 months | 0.66 | |||
IMpower110 | squamous (25%) and nonsquamous (75%) | ≥50% | Atezolizumab | Cisplatin/Carboplatin + Gemcitabine (for squamous) or pemetrexed (nonsquamous) |
|
20.2 months | 13.1 months | 0.59 | |||
IMpower130 | non-squamous | Any level | Atezolizumab & Carboplatin +nab-paclitaxel | Carboplatin +nab-paclitaxel | |
18.6 months | 13.9 months | 0.79 | |||
IMpower150 | non-squamous | Any level | Atezolizumab + Bevacizumab + Carboplatin, and Paclitaxel | Bevacizumab + Carboplatin, and Paclitaxel | |
19.8 months | 14.9 months | 0.76 |