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Author(s):
Julie R. Brahmer, MD, associate professor of oncology, co-director of the Upper Aerodigestive Department, Bloomberg Kimmel Institute for Cancer Immunotherapy, Johns Hopkins Medicine, discusses biomarkers for immune response in non–small cell lung cancer.
Julie R. Brahmer, MD, associate professor of oncology, co-director of the Upper Aerodigestive Department, Bloomberg Kimmel Institute for Cancer Immunotherapy, Johns Hopkins Medicine, discusses biomarkers for immune response in non—small cell lung cancer (NSCLC).
Data from the KEYNOTE-024 study demonstrated that patients with high tumor proportion score and a PD-L1 status of >50% seemed more likely to derive clinical benefit from single-agent pembrolizumab (Keytruda). Brahmer says although PD-L1 expression is an effective biomarker with immunotherapy alone, it becomes more inconsistent when checkpoint inhibitors are combined with chemotherapy. Another challenge with detecting PD-L1 expression is having enough tissue available to test for it, she adds.
In that regard, tumor mutational burden (TMB) may be a little more advantageous as a biomarker in the space. If TMB can easily be detected with a liquid biopsy, that can lead to advances in turnaround time and allow for a more personalized treatment approach for patients.