Nivolumab |
CHECKMATE-577 |
Adjuvant (after neoadjuvant chemoradiation + surgery with residual pathological disease) |
2021 (FDA, EMA) |
Nivolumab |
CHECKMATE-577 |
Adjuvant (after neoadjuvant chemoradiation + surgery with residual pathological disease) |
2021 (FDA, EMA) |
Nivolumab + platine or fluoropyrimidine-based chemotherapy |
CHECKMATE-649 |
1st line, metastatic, recurrent or inoperable |
2021 (FDA) |
Pembrolizumab + platine or fluoropyrimidine-based chemotherapy |
KEYNOTE-590 |
1st line metastatic, recurrent or inoperable |
2021 (FDA, EMA for CPS ≥ 10) |
Pembrolizumab + platine or fluoropyrimidine-based chemotherapy |
KEYNOTE-590 |
1st line, metastatic, recurrent or inoperable |
2021 (FDA, EMA for CPS ≥ 10) |
Nivolumab |
ATTRACTION-3 |
2nd and further-line metastatic, recurrent or inoperable |
2020 (FDA, EMA) |
|
|
|
|
Pembrolizumab |
KEYNOTE-181 |
2nd and further-line metastatic, recurrent or inoperable, CPS ≥ 10 |
2019 (FDA) |