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editorial
. 2018 Nov;10(Suppl 33):S4096–S4100. doi: 10.21037/jtd.2018.10.24

Table 1. PD-L1 testing methods.

PD-L1 antibody Platform Detection system Agent Cut-off
   NSCLC   HNSCC   UC
SP263 Ventana BenchMark Ultraa OptiView DAB IHC Detection Kita Durvalumabb    TC: ≥25%   TC: ≥25%   TC or IC: ≥25%
22C3 Dako Autostainer Link 48c EnVision FLEX visualization systemc Pembrolizumabd    TC: ≥1%, ≥50% TPS   TC or IC: >1%, >50%   TC and IC: ≥10% TPS
28-8 Dako Autostainer Link 48 EnVision FLEX visualization system Nivolumabe    TC: >1%, >5%   >1%, >5%   TC: >1%, >5%
SP142 Ventana BenchMark Ultra OptiView DAB IHC Detection Kit and OptiView Amplification Kita Atezolizumabf    TC: ≥10%, IC: ≥50%   TC: ≥5%, IC: ≥5%   IC: ≥5%
73-10 Dako Autostainer Link 48 EnVision FLEX visualization system Avelumabd,g    TC: ≥1%, 50%, 80%   NA   TC: ≥5%

a, Ventana Medical Systems, Tucson, AZ, USA; b, Agilent Technologies, Mississauga, ON; c, AstraZeneca, Cambridge, UK; d, Merck, Kenilworth, NJ, USA; e, Bristol-Myers Squibb, New York, NY, USA; f, Roche, Basel, Switzerland; g, Pfizer, New York, NY, USA. NSCLC, non-small cell lung cancer; HNSCC, head-and-neck squamous cell carcinoma; UC, urothelial carcinoma; IHC, immunohistochemistry; TC, tumour cell; IC, immune cell; TPS, tumour proportion score (PD-L1-expressing TCs and infiltrating ICs relative to the total number of TCs); NA, not applicable.