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2016 DEPARTMENT OF MEDICINE RESEARCH DAY Title of Poster: Evaluation of PD-L1 expression on vortex-isolated circulating tumor cells and comparison to response Presenter: Rajan Kulkarni Division: Dermatology ☒ Faculty ☐ Fellow ☐ Resident ☐ Post-doc Research Fellow ☐ Graduate Student ☐ Medical Student ☐Other Principal Investigator/Mentor: Rajan Kulkarni Co-Investigators: Manjima Dhar, James Che, Edward Garon, Melissa Matsumoto, Brian Wolf, Steven Dubinett, James Carroll, Jonathan Goldman, Elodie Sollier, Dino Di Carlo Thematic Poster Category: Development, Morphogenesis, Cell Growth and Differentiation, Apoptosis, Stem Cell Biology, Carcinogenesis and Cancer Biology Abstract Metastatic non-small cell lung cancer (NSCLC) is a highly fatal and immunogenic malignancy. Although the immune system is known to recognize these tumor cells, one mechanism by which NSCLC can evade the immune system is via overexpression of programmed cell death ligand 1 (PD-L1). Recent clinical trials investigating efficacy of PD-1 and PD-L1 inhibitors have returned promising clinical responses. Important for personalizing therapy, patients with higher intensity staining for PD-L1 on tumor biopsies responded better than others. Thus there has been interest in using PD-L1 tumor expression as a selection criteria. Currently available methods of screening involve invasive tumor biopsy followed by histological grading of PD-L1 levels. Since biopsies only allow sampling from limited sections of the tumor, which may not reflect overall tumor heterogeneity, circulating tumor cell (CTC) PD-L1 levels could aid in screening patients, and could supplement tissue PD-L1 biopsy results by testing PD-L1 expression from disseminated tumor sites. Towards establishing the use of CTCs as a screening tool, we developed a protocol to isolate at high purity and immunostain for PD-L1 on CTCs. We compared CTC expression of PD-L1 with corresponding tumor expression and with treatment response evaluated by immune related response criteria (irRC). Monitoring of PD-L1 expression on CTCs could be an additional biomarker for precision medicine that may help in determining response to immunotherapies.