Table 2.
Results about prognostic value of PD-L1 expression in HNSCC clinical trials
Reference |
Year |
Protocol |
Cells analyzed |
Clone of antibody |
Cutoff |
of PD-L1+ |
Correlation with anti-PD1 response |
Ferris et al. NEJM | 2017 | Checkmate 141 | TC | clone 28–8, Epitomics | ≥1% | 149 | + |
≥5% | 97 | + | |||||
≥10% | 77 | - | |||||
Ferris et al. OO | 2016 | Checkmate 141 | TC | clone 28–8, Epitomics | ≥1% | 55 | + |
≥5% | 34 | + | |||||
≥10% | 27 | - | |||||
Seiwert et al. | 2016 | KEYNOTE-012 | TC and IC | 22C3, Merck | ≥1 | 100% | NEV |
Chow et al. | 2016 | KEYNOTE-012 | TC | 22C3, Merck | ≥1% | 67% | - |
TC and IC | ≥1 | 81% | + | ||||
Bauml et al. | 2017 | KEYNOTE-055 | TC and IC | 22C3, Merck | ≥1 | 84% | + |
≥50 | 29% | + | |||||
Cohen et al. | 2018 | KEYNOTE-040 | TC and IC | 22C3, Merck | ≥1 | 78% | + |
Burtness et al. | 2018 | KEYNOTE-048 | TC and IC | 22C3, Merck | ≥1 | 85% | + |
≥20 | 40% | + |
IC, immune cells; TC, tumor cells