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Expression of PD-1 and PD-L1 in Anaplastic Thyroid Cancer Patients Treated With Multimodal Therapy: Results From a Retrospective Study.

Authors :
Chintakuntlawar AV
Rumilla KM
Smith CY
Jenkins SM
Foote RL
Kasperbauer JL
Morris JC
Ryder M
Alsidawi S
Hilger C
Bible KC
Source :
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2017 Jun 01; Vol. 102 (6), pp. 1943-1950.
Publication Year :
2017

Abstract

Context: Anaplastic thyroid cancer (ATC) is rare and a highly fatal malignancy. The role of programmed death-1 (PD-1) and programmed death ligand-1 (PD-L1) as prognostic and/or predictive markers in ATC is unknown.<br />Objective: Multimodal therapy offers the best chance at tumor control. The objective of this study was to detect potential associations of PD-1/PD-L1 axis variables with outcome data in ATC.<br />Design: Retrospective study of a uniformly treated cohort.<br />Setting: Single institution retrospective cohort study.<br />Patients or Other Participants: Sixteen patients who received intensity-modulated radiation therapy (15 had preceding surgery) were studied.<br />Main Outcome Measure: Patients treated with multimodal therapy were followed and assessed for overall survival (OS) and progression-free survival (PFS).<br />Results: All samples demonstrated PD-1 expression in inflammatory cells whereas tumor cells were primarily negative. PD-L1 was expressed on ATC tumor cells in most samples and showed mainly membranous staining. High PD-1 expression (>40% staining) in inflammatory cells was associated with worse overall survival (OS; hazard ratio, 3.36; 95% confidence interval, 1.00 to 12.96; P < 0.05) and trended toward worse PFS, whereas high PD-L1 expression in tumor cells (>33% staining) trended toward worse PFS and OS.<br />Conclusion: PD-1/PD-L1 pathway proteins are highly expressed in ATC tumor samples and appear to represent predictive markers of PFS and OS in multimodality-treated ATC patients.<br /> (Copyright © 2017 Endocrine Society)

Details

Language :
English
ISSN :
1945-7197
Volume :
102
Issue :
6
Database :
MEDLINE
Journal :
The Journal of clinical endocrinology and metabolism
Publication Type :
Academic Journal
Accession number :
28324060
Full Text :
https://doi.org/10.1210/jc.2016-3756