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TEST:
VENTANA PD-L1 (SP263) Assay

Company:
Roche
Type:
FDA Approved
Related tests:
VENTANA PD-L1 (SP263) Assay is an IVD qualitative immunohistochemical assay using rabbit monoclonal anti-PD-L1 clone SP263 intended for use in the assessment of the PD-L1 protein in formalin-fixed, paraffin-embedded (FFPE) urothelial carcinoma tissue stained with OptiView DAB IHC Detection Kit on a VENTANA BenchMark ULTRA instrument. PD-L1 status is determined by the percentage of tumor cells with any membrane staining above background or by the percentage of tumor-associated immune cells with staining (IC+) at any intensity above background. The percent of tumor area occupied by any tumor-associated immune cells (Immune Cells Present, ICP) is used to determine IC+, which is the percent area of ICP exhibiting PD-L1 positive immune cell staining. PD-L1 status is considered High if any of the following are met: ≥ 25% of tumor cells exhibit membrane staining; or, ICP > 1% and IC+ ≥ 25%; or, ICP = 1% and IC+ = 100%. PD-L1 High status as determined by VENTANA PD-L1 (SP263) Assay was associated with increased objective response rate (ORR) in a single arm study of IMFINZI™ (durvalumab).
Cancer:
Non Small Cell Lung Cancer, Urothelial Cancer
Gene:
PD-L1 (Programmed death ligand 1)
Drug:
Imfinzi (durvalumab), Libtayo (cemiplimab-rwlc), Tecentriq (atezolizumab)
Method:
Immunohistochemistry (IHC)
Approvals
Date
Cancer
Gene
Drug
By