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Tumor necrosis correlates with PD-L1 and PD-1 expression in lung adenocarcinoma

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posted on 2019-04-19, 11:34 authored by Lilla Reiniger, Vanda Téglási, Orsolya Pipek, Lívia Rojkó, Tibor Glasz, Attila Vágvölgyi, Ilona Kovalszky, Márton Gyulai, Zoltán Lohinai, Erzsébet Rásó, József Tímár, Balázs Döme, Zoltán Szállási, Judit Moldvay

Background: Predictive biomarkers for immunotherapy in lung cancer are intensively investigated; however, correlations between PD-L1/PD-1 expressions and clinical features or histopathological tumor characteristics determined on hematoxylin and eosin stained sections have not extensively been studied.

Material and methods: We determined PD-L1 expression of tumor cells (TC) and immune cells (IC), and PD-1 expression of IC by immunohistochemistry in 268 lung adenocarcinoma (LADC) patients, and correlated the data with smoking, COPD, tumor grade, necrosis, lepidic growth pattern, vascular invasion, density of stromal IC, and EGFR/KRAS status of the tumors.

Results: There was a positive correlation between PD-L1 expression of TC and IC, as well as PD-L1 and PD-1 expression of IC. Tumor necrosis was associated with higher PD-L1 expression of TC and PD-1 expression of IC. A negative correlation was observed between lepidic growth pattern and PD-L1 expression of TC and PD-L1/PD-1 expression of IC. EGFR mutation seemed to negatively correlate with PD-1 expression of IC, but this tendency could not be verified when applying corrections for multiple comparisons. No significant effect of the KRAS mutation on any of the studied variables could be established.

Conclusion: Here we first demonstrate that the presence of necrosis correlates with higher PD-L1 expression of TC and PD-1 expression of IC in LADC. Further studies are required to determine the predictive value of this observation in LADC patients receiving immunotherapy.

Funding

This work was supported by the Research and Technology Innovation Fund (KTIA_NAP_13-2014-0021 to L.R., Z.S., and NAP2-2017-1.2.1-NKP-0002 to L.R., Z.S., J.T., J.M.); Hungarian Science Foundation (OTKA-PD115792 to L.R., OTKA-K116151 to L.R., J.T., B.D., OTKA-K112371 to J.T., OTKA-K129065 to D.B., J.M.); Breast Cancer Research Foundation and the Novo Nordisk Foundation Interdisciplinary Synergy Programme Grant (NNF15OC0016584 to Z.S.). For the remaining authors none were declared.

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