Table 1.
Checkpoint | Blocking agent | IgG isotype and characteristics | Clinical stage | Manufacturer |
---|---|---|---|---|
PD-1 | Pembrolizumab | Humanized IgG4 mAb | EMA, FDA approved for first-line and second-line NSCLC treatment | Merck |
Nivolumab | Humanized IgG4 mAb | FDA approved for second-line NSCLC | Bristol-Myers Squibb | |
Toripalimab | Humanized IgG4 mAb | Clinical trial ongoing | Shanghai Junshi | |
Sintilimab | Fully human IgG4 mAb | Clinical trial ongoing | Innovent Biologics | |
Camrelizumab | Humanized IgG4 mAb | Clinical trial ongoing | Hengrui Medicine | |
Tislelizumab | Humanized IgG4 mAb | Clinical trial ongoing | BeiGene | |
PDR001 | Humanized IgG4 mAb | Clinical trial ongoing | Novartis | |
REGN2810 | Humanized IgG4 mAb | Clinical trial ongoing | Regeneron-Sanofi | |
PD-L1 | Atezolizumab | High-affinity human IgG1 | FDA approved for second-line NSCLC | Roche |
Durvalumab | Human IgG1 mAb | FDA approved for treatment of unresectable stage III NSCLC without relapse after chemoradiation | AstraZeneca | |
BMS-936559 | Fully high-affinity human IgG4 | Clinical trial ongoing | Bristol-Myers Squibb |
EMA, European Medicines Agency; FDA, US Food and Drug Administration; IgG, immunoglobulin G; mAb, monoclonal antibody; NSCLC, non-small-cell lung cancer; PD-1, programmed cell-death protein 1; PD-L1, programmed cell-death ligand 1.