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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.