Table 1.
Prospective trials in neoadjuvant immuno(chemo)therapy.
| Trial | Stage | Neoadjuvant treatment | Duration (cycles) | n | Resected | MPR (%) | cPR (%) |
|---|---|---|---|---|---|---|---|
| Phase II | |||||||
| CheckMate-1596,7 | I-IIIA | Nivolumab | 2 | 22 | 20 | 45 | 15 |
| LCMC3 8 | IB-IIIB | Atezolizumab | 2 | 93 | 82 | 18 | 5 |
| IONESCO 9 | IB-IIB | Durvalumab | 3 biweekly | 50 | 43 a | 19 | 7 |
| NEOMUN 10 | II-IIIA | Pembrolizumab | 2 | 15 | 15 | 27 | 18 |
| Reuss 11 | IB-IIIA | Ipilimumab and nivolumab | 3 biweekly | 9 | 6 b | NA | 33 |
| NEOSTAR 12 | I-IIIA | Ipilimumab and nivolumab versus nivolumab | 3 biweekly | 44 | 34 | 29 versus 17 | 19 versus 9 |
| Shu 13 | IB-IIIA | Atezolizumab, carboplatin, and nab-paclitaxel | 4 | 30 | 29 | 57 | 33 |
| NADIM14,15 | Nivolumab, carboplatin, and paclitaxel | 3 | 46 | 41 | 80 | 63 | |
| Phase III: | |||||||
| CheckMate-81616,17 | IB-IIIA | Platinum-doublet and nivolumab versus platinum-doublet | 3 | 2 × 158 | 149 versus 135 | 36.9 versus 8.9% | 24.2% versus 2.2% |
MPR, major pathological response.
Early termination because of five post-operative deaths.
Terminated early due to toxicity.