Table 4.
NCT Number/Trial Name | Study Phase | Patients | IO Agent | Trial Design | RT Dose | RT and IO Timing | Status |
---|---|---|---|---|---|---|---|
NCT03237377 | II Single arm |
Resectable Stage IIIA NSCLC | Durvalumab ± tremelimumab | Neoadjuvant IO + RT, followed by surgery | 45 Gy/25 fx | Concurrent | Recruiting |
NCT04245514 | II Single arm with 3 radiotherapy cohorts |
Resectable Stage IIIA NSCLC | Durvalumab | Neoadjuvant IO + RT followed by surgery | Allocated in a 1:1:1 ratio: Arm A: 20 × 2 Gy Arm B: 5 × 5 Gy Arm C: 3 × 8 Gy |
Concurrent | Recruiting |
NCT02987998 | I | Resectable Stage IIIA NSCLC | Pembrolizumab | Neoadjuvant chemoRT (cisplatin-etoposide) + IO, followed by surgery, followed by consolidation IO | 45 Gy/25 fx | Concurrent | Active, not recruiting |
NCT02904954 | II Randomised |
Resectable Stage I-IIIA NSCLC |
Durvalumab | Neoadjuvant IO ± SBRT, followed by surgery, followed by postoperative maintenance IO | SBRT to 24 Gy/3 fx | Concurrent | Active, not recruiting |
NCT03871153 | II Single arm |
Resectables Stage IIIA NSCLC | Durvalumab | Neoadjuvant chemoRT (carboplatin–paclitaxel) + IO followed by surgery | 45–61.2 Gy 1.8–2.0 Gy per day |
Recruiting |
IO = immunotherapy; RT = radiotherapy; NSCLC = non-small-cell lung cancer; Gy = grays; fx = fractions; SBRT = stereotactic body radiation therapy.