4.4 Article

PD-L1 Expression of Lung Cancer Cells, Unlike Infiltrating Immune Cells, Is Stable and Unaffected by Therapy During Brain Metastasis

Journal

CLINICAL LUNG CANCER
Volume 20, Issue 5, Pages 363-+

Publisher

CIG MEDIA GROUP, LP
DOI: 10.1016/j.cllc.2019.05.008

Keywords

Immune checkpoint; Immune environment; Lung adenocarcinoma; Programmed death ligand 1

Categories

Funding

  1. Hungarian Brain Research Program [2017-1.2.1-NKP-2017-00002]
  2. Breast Cancer Research Foundation [BCRF-17-156]
  3. Novo Nordisk Foundation Interdisciplinary Synergy Programme [NNF15OC0016584]
  4. Hungarian National Research, Development and Innovation Office [NVKP_16-1-2016-0004]
  5. Hungarian Science Foundation [OTKA-K116151]
  6. Hungarian National Research, Development and Innovation (NRDI) Office [K109626, SNN114490]
  7. Austrian Science Fund [FWF I 3977]
  8. Hungarian NRDI Office [K129065]

Ask authors/readers for more resources

Patient selection criteria for immune checkpoint inhibitor therapy is still debated. We compared the immune cell infiltration and programmed cell death 1 (PD-1)/programmed death ligand 1 (PD-L1) expression of primary lung adenocarcinoma with their corresponding brain metastasis and found a strong correlation of PD-L1- positive tumor cells not influenced by oncotherapies. PD-L1 positivity in the primary tumor could serve as a therapeutic criterion even for brain metastases. Background: Approximately 50% of brain metastases originate from non-small-cell lung cancer. The median survival of patients with brain metastases is 1 month without treatment. Novel immunotherapeutic strategies, such as those targeting the programmed death ligand 1 (PD-L1)/programmed cell death 1 (PD-1) axis, are promising in patients with advanced systemic disease but are often preferentially administered to patients with tumors showing PD-L1 positivity. Patients and Methods: Surgically resected paired primary lung adenocarcinoma and brain metastasis samples of 61 patients were analyzed. We compared the paired samples regarding the amount of peritumoral and stromal mononuclear infiltration, PD-L1 expression of tumor and immune cells, and PD-1 expression of immune cells. We investigated the effect of radiotherapy, chemotherapy, and steroid therapy on PD-L1 expression in brain metastases. Results: There was significant positive correlation regarding the PD-L1 expression of tumor cells between the paired primary lung adenocarcinoma and brain metastatic samples with the use of different cutoff levels (1%, 5%, 50%). We found no impact of chemotherapy or steroid therapy on the changes of PD-L1 expression of tumor cells between the 2 sites. There is no or only limited concordance of the proportion of PD-1- or PD-L1-positive tumor-associated immune cells between the paired tumor samples, which suggests that brain metastases develop their own immune environment. Conclusion: We observed a strong correlation of PD-L1 positive tumor cells between primary lung adenocarcinoma cases and their corresponding brain metastases, which is not significantly influenced by chemotherapy or steroid therapy. (C) 2019 Elsevier Inc. All rights reserved.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.4
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available