The VENTANA PD-L1 (SP142) Assay is a CDx that’s FDA approved to help identify triple-negative breast cancer (TNBC) patients eligible for TECENTRIQ® (atezolizumab).1,2 You can run this assay on your BenchMark ULTRA system or send it to one of our testing centers.
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Learn about the tumor microenvironment, PD-L1 expression on immune and tumor cells and the development process for companion diagnostic tests.
Watch our online microscopy training, “Scoring the VENTANA PD-L1 (SP142) Assay for the TNBC indication,” hosted by Roche Medical and Scientific Affairs Pathologists.
Find online training courses for the VENTANA PD-L1 (SP142) Assay. Topics include PD-L1 expression, the tumor microenvironment and information on the other cancer indications.
The VENTANA PD-L1 (SP142) Assay* is an FDA-approved test predictive for TECENTRIQ® (atezolizumab) in urothelial carcinoma (UC) patients. It is also the first to evaluate patient PD-L1 expression using immune cell staining and scoring within the tumor microenvironment, providing you with information that can guide immunotherapy decisions.
*In the US available only on the VENTANA BenchMark ULTRA automated slide staining instrument.
The VENTANA PD-L1 (SP142) Assay gives you confidence to reliably identify non-small cell lung cancer patients eligible for TECENTRIQ.®
