PD-L1 expression on circulating tumor cells and platelets in patients with metastatic breast cancer

Immune checkpoint inhibition is effective in several cancers. Expression of programmed death-ligand 1 (PD-L1) on circulating tumor or immune effector cells could provide insights into selection of patients for immune checkpoint inhibition. Whole blood was collected at serial timepoints from metastat...

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Veröffentlicht in:PloS one 2021-11, Vol.16 (11), p.e0260124-e0260124
Hauptverfasser: Darga, Elizabeth P, Dolce, Emily M, Fang, Fang, Kidwell, Kelley M, Gersch, Christina L, Kregel, Steven, Thomas, Dafydd G, Gill, Anoop, Brown, Martha E, Gross, Steven, Connelly, Mark, Holinstat, Michael, Cobain, Erin F, Rae, James M, Hayes, Daniel F, Paoletti, Costanza
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Sprache:eng
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Zusammenfassung:Immune checkpoint inhibition is effective in several cancers. Expression of programmed death-ligand 1 (PD-L1) on circulating tumor or immune effector cells could provide insights into selection of patients for immune checkpoint inhibition. Whole blood was collected at serial timepoints from metastatic breast cancer patients and healthy donors for circulating tumor cell (CTC) and platelet PD-L1 analysis with a phycoerythrin-labeled anti-human PD-L1 monoclonal antibody (Biolegend clone 29E.2A3) using the CellSearch® assay. CTC PD-L1 was considered positive if detected on at least 1% of the cells; platelet PD-L1 was considered positive if ≥100 platelets per CellSearch frame expressed PD-L1. A total of 207 specimens from 124 metastatic breast cancer patients were collected. 52/124 (42%) samples at timepoint-1 (at or close to time of progressive disease) had ≥5 CTC/7.5ml whole blood. Of those, 21 (40%) had positive CTC PD-L1. In addition, platelet PD-L1 expression was observed in 35/124 (28%) at timepoint-1. Platelet PD-L1 was not detected in more than 70 specimens from 12 healthy donors. Platelet PD-L1 was associated with ≥5 CTC/7.5ml whole blood (p = 0.0002), less likely in patients with higher red blood cell counts (OR = 0.72, p
ISSN:1932-6203
1932-6203
DOI:10.1371/journal.pone.0260124