Relationship of tumor PD-L1 expression with EGFR wild-type status and poor prognosis in lung adenocarcinoma

Programmed death-ligand 1 is an immune modulator that promotes immunosuppression by binding to programmed death-1 of T-lymphocytes. Whereas programmed death-ligand 1 expression has been shown to be associated with the clinical response to anti-programmed death-ligand 1 antibody, the association of t...

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Veröffentlicht in:Japanese journal of clinical oncology 2016-10, Vol.46 (10), p.935-941
Hauptverfasser: Inamura, Kentaro, Yokouchi, Yusuke, Sakakibara, Rie, Kobayashi, Maki, Subat, Sophia, Ninomiya, Hironori, Nagano, Hiroko, Nomura, Kimie, Okumura, Sakae, Ishikawa, Yuichi
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Sprache:eng
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Zusammenfassung:Programmed death-ligand 1 is an immune modulator that promotes immunosuppression by binding to programmed death-1 of T-lymphocytes. Whereas programmed death-ligand 1 expression has been shown to be associated with the clinical response to anti-programmed death-ligand 1 antibody, the association of tumor programmed death-ligand 1 expression with clinicopathological/molecular features and with prognosis remains inconclusive in lung adenocarcinoma. We therefore examined the association of programmed death-ligand 1 expression with the clinicopathological/molecular features and prognosis of lung adenocarcinoma. Using tissue microarrays of 268 consecutive cases of lung adenocarcinoma, we evaluated programmed death-ligand 1 expression by immunohistochemistry. We examined the association of programmed death-ligand 1 expression with clinicopathological and molecular features. We also examined the prognostic association of programmed death-ligand 1 expression, using the log-rank test as well as Cox proportional hazards regression models to compute the mortality hazard ratio (HR). Programmed death-ligand 1 immunoreactivity (at least 5% of the tumor cells) was observed in 43 (16%) of 268 cases of lung adenocarcinoma. Programmed death-ligand 1 positivity was associated with less tumor differentiation (P 
ISSN:0368-2811
1465-3621
DOI:10.1093/jjco/hyw087