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. 2018 Jul 11;10:1758835918786228. doi: 10.1177/1758835918786228

Table 2.

Key examples of ICPI FDA companion diagnostic approvals.

IPCI Drug class PD-L1 antibody companion diagnostic FDA licensed indications Detection on immune cells/tumour cells Study references
Pembrolizumab PD-1 inhibitor 22C3 (DAKO) NSCLC first line TPS ⩾ 50% Reck et al.31
NSCLC ⩾ second line TPS ⩾ 1% Herbst et al.32
Metastatic OGJ/gastric cancer > second line CPS ⩾ 1% Fuchs et al.33
Companion diagnostic not required in license but benefit shown in stated subpopulations
Nivolumab PD-1 inhibitor 28-8 (DAKO) NSCLC ⩾ second line TC ⩾ 1% Borghaei et al.34
Atezolizumab PD-L1 inhibitor SP142 (Ventana) NSCLC ⩾ second line TC or TI ICs ⩾ 1% Rittmeyer et al.35
Urothelial cancer ⩾ second line or first line in those patients unfit for cisplatin ⩾ 5% TI ICs Powles et al.36
Durvalumab PD-L1 inhibitor SP263 (Ventana) Urothelial cancer ⩾ second line or first line in those patients unfit for cisplatin IC > 1%:
TC or IC ⩾ 25%
or
IC ⩽ 1%:
TC ⩾ 25% or IC = 100%
Powles et al.37

CPS = number of PD-L1 staining cells (tumour cells, lymphocytes, macrophages)/total cells × 100.

IC, immune cell; FDA, US Food and Drug Administration; NSCLC, non-small cell lung cancer; OGJ, oesophagogastric junction; PD-L1, programmed death ligand 1; TC, tumour cell; TI IC, tumour-infiltrating immune cell; TPS, tumour proportion score; CPS, combined proportion score.