VENTANA PD-L1 (SP263) Assay (FDA Approved)

Predictive IHC assay

PD-L1 SP263 Assay UC stain image
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Empowering pathologists to answer PD-L1 questions
VENTANA PD-L1 (SP263) Assay guides immunotherapy decisions by identifying:

 

  • Non-small cell carcinoma (NSCLC) patients eligible for treatment with TECENTRIQ® (atezolizumab)
  • NSCLC patients eligible for treatment with LIBTAYO® (cemiplimab)
VENTANA PD-L1 (SP263) Assay further benefits patients by:

 

  • Providing robust PD-L1 staining in both tumor cells (TC) and tumor-infiltrating immune cells (IC)
  • Allowing optimal lung tissue management through PD-L1 testing of archived unstained slides within 12 months
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Reagent and ancillary product information

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VENTANA PD-L1 (SP263) Assay is a qualitative immunohistochemistry assay using rabbit monoclonal anti-PD-L1 clone SP263 intended for use in the assessment of the programmed death ligand-1 (PD-L1) protein in formalin-fixed, paraffin-embedded (FFPE) non-small cell lung carcinoma (NSCLC) tissue specimens by light microscopy. The VENTANA PD-L1 (SP263) Assay is used with the OptiView DAB IHC Detection Kit for staining on the BenchMark ULTRA instrument.

NSCLC:

PD-L1 expression in tumor cell (TC) membrane as detected by VENTANA PD-L1 (SP263) Assay in NSCLC is indicated as an aid in identifying patients for treatment with TECENTRIQ® (atezolizumab).

PD-L1 expression in tumor cell (TC) membrane as detected by VENTANA PD-L1 (SP263) Assay in NSCLC is indicated as an aid in identifying patients for treatment with LIBTAYO® (cemiplimab).

Table 1. Therapy and associated indication.

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Table 1. Therapy and associated indication.

Indication for use Therapy PD-L1 Expression
NSCLC TECENTRIQ® ≥1 % TC
LIBTAYO® ≥50 % TC
*Please refer to the VENTANA PD-L1 (SP263) Assay method sheet for the full intended use statement and approved therapeutic labeling.
IC staining with this assay is not used to assess PD-L1 status in NSCLC.