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. Author manuscript; available in PMC: 2016 Jun 6.
Published in final edited form as: Cancer J. 2014 Jul-Aug;20(4):272–280. doi: 10.1097/PPO.0000000000000055

TABLE 4.

Summary of PD-L1 Expression and Correlation With Objective Responses in the RCC and Melanoma Trials

Tumor
Type
Agent No. With
Tissue
Definition
of PD-L1+ *
% PD-L1+ (n) ORR
PD-L1+ (n)
ORR
PD-L1- (n)
IHC
Antibody/
Miscellaneous
Brahmer et al46 Solid tumors Nivolumab 9 ≥5% 44% (4/9) 75% (3/4) 0% (0/5) L. Chen
Topalian et al47 Solid tumors Nivolumab 42 (5 RCC, 18 melanoma) ≥5% 60% (25/42) 36% (9/25) 0% (0/17) L. Chen
Cho et al58 RCC MPDL3280A 31 ≥5% 33% (10/31) 20% (2/10) 10% (2/21) Genentech Ab
Hamid et al59 Melanoma MPDL3280A 38 ≥5% 39% (15/38) 27% (4/15) 20% (3/15) Genentech Ab
Weber et al51 Melanoma Nivolumab 44 >5% 27% (12/44) 67% (8/12) 19% (6/32) P = 0.004
>1% 54% (23/44) 39% (9/23) 23% (5/21)
Wolchok et al55 Melanoma Nivolumab + ipilimumab 56 ≥5% 38% (21/56) Clone 28-8§
Concurrent 46% (6/13) 41% (9/22) P > 0.99, NSS
Sequential 50% (4/8) 8% (1/13)
*

PD-L1 testing was generally done on the tumor cells with the exception of MPDL3280A in which case the investigators reported the PD-L1 positivity of the tumor infiltrating immune cells.

Murine anti-human B7-H1 (PD-L1) monoclonal antibody clone 5H1.

Statistically significant.

§

Rabbit monoclonal antihuman PD-L1 antibody known as clone 28-8 and Dako’s automated assay.

Ab indicates antibody; IHC, immunohistochemistry; NSS, not statistically significant.