Effectiveness of PD-L1 Tests Compared for Non-Small-Cell Lung Cancer

They found that one assay failed to result in comparable levels of PD-L1, while the three other assays resulted in comparable levels.

The assays are used to test expression of PD-L1 on a patient’s tumor to help customize treatment options using drugs that may be more effective against lung cancer than chemotherapy. Findings of the new study were presented September 26, 2016, by researchers from Yale Cancer Center (New Haven, CT, USA) at the International Association for the Study of Lung Cancer (IASLC) 2016 Chicago Multidisciplinary Symposium in Thoracic Oncology (Chicago, USA). The study was sponsored by Bristol Myers Squibb with the National Comprehensive Cancer Network (NCCN) Oncology Research Program.

The team reviewed 90 surgically resected NSCLC cases (stages I-III) and sent a sample of each to four facilities for staining. A group of 13 pathologists at 7 institutions then reviewed the samples, using 4 different assays on each case, and scored them using a unified scoring system. A comprehensive statistical analysis was then performed on the scores collected.

Currently available are four drugs with four PD-L1 assays: 22c3, 28-8, E1L3N, and SP142. However only the 22c3 test is required by the US Food & Drug Administration (FDA) for prescription of a targeted anti-PD-1 drug (pembrolizumab), while the other tests are not yet required for prescription of other PD-1 axis drugs. The study revealed that SP142 systematically returned statistically lower levels of PD-L1 expression than the other three tests. This was true in both tumor and immune cells using any test. The other three available assays (28-8, E1L3N, and 22c3) showed no significant difference between them.

“Our data shows that the SP142 assay shows significantly lower levels of PD-L1 expression. This observation may limit the use of this assay in PD-L1 testing moving forward,” said first author David L. Rimm, MD, PhD, professor at Yale School of Medicine, “However, the other three assays seem equivalent, which is good news for the future when other PD-1 axis drugs with assay-specific diagnostics gain FDA approval.”

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