SOLUBLE FORMS OF PD-1 AND PD-L1 IN BLOOD PLASMA OF GASTRIC CANCER PATIENTS AND THEIR ASSOCIATIONS WITH CLINICAL AND MORPHOLOGICAL CHARACTERISTICS OF THE DISEASE
Authors:
- E. S. GershteinEGE. S. Gershtein
- N. A. OgnerubovNON. A. Ognerubov
- V. L. ChangVCV. L. Chang
- V. V. DelektorskayaVDV. V. Delektorskaya
- E. A. KorotkovaEKE. A. Korotkova
- N. Yu. SokolovNSN. Yu. Sokolov
- S. B. PolikarpovaSPS. B. Polikarpova
- I. S. StilidiISI. S. Stilidi
- Nikolay Evgenievich KushlinskiiNKNikolay Evgenievich Kushlinskii
Open Access
- 15 May 2020
- journal article
- abstracts
- Published by EKOlab in Russian Clinical Laboratory Diagnostics
- Vol. 65 (6) , 347-352
Abstract
Results of comparative ELISA investigation of pretreatment sPD-1 and sPD-L1 content in blood plasma of 100 gastric cancer patients at various disease stages aged 25 to 81 years are presented. Control group included 60 practically healthy donors aged 18 - 68 years. Plasma sPD-L1 concentrations did not differ between gastric cancer patients and control group, and sPD-1 levels were statistically significantly lower in patients than in healthy donors (p<0.0001). Positive correlation (R=0.38; p=0.003) was revealed between plasma sPD-1 and sPD-L1 levels in control group and negative (R= -0.26; p=0,009) - in gastric cancer patients. ROC curve revealed the best sPD-1 cut-off level (< 21 pg/ml) with 77% sensitivity and 63.3% specificity, which is not sufficient for its application as diagnostic marker. Statistically significant increase of plasma sPD-L1 from stage I to stage IIIC (R=0.50; p=0.000011) was found. Analysis of associations between the evaluated markers’ levels and indices of gastric cancer expansion according to TNM system revealed statistically significant positive associations of plasma sPD-L1 levels with T (tumor invasion depth) and N (number of affected lymph nodes) indices: R=0.33; p=0.00093, and R=0.27; p=0.0099 respectively. sPD-L1 level was significantly increased in patients with low differentiated adenocarcinoma and cricoid-cell cancer as compared to highly differentiated adenocarcinoma (p=0.02 and p=0.004 respectively); in patients with cricoid-cell cancer it was also higher than in those with moderately differentiated adenocarcinoma (p=0.043) and undifferentiated cancer (p=0.049). Plasma sPD-1 level did not depend on disease stage, TNM system indices and tumor histological structure. Thus, soluble ligand sPD-L1, but not its receptor sPD-1, plasma level is increased in patients with unfavorable clinical and morphological characteristics, may be regarded as potentially valuable prognostic factor for gastric cancer patients’ survival, and probably as a predictor of anti - PD-1/PD-L1 treatment efficiency.Keywords
This publication has 15 references indexed in Scilit:
- Antitumor Effect of Nivolumab on Subsequent Chemotherapy for Platinum-Resistant Ovarian CancerThe Oncologist, 2018
- Modern approaches to kidney cancer immunotherapyCancer Urology, 2018
- Evaluation of programmed cell death protein 1 (PD-1) expression as a prognostic biomarker in patients with clear cell renal cell carcinomaOncoImmunology, 2018
- Prognostic Value of Programmed Cell Death 1 Ligand-1 (PD-L1) or PD-1 Expression in Patients with Osteosarcoma: A Meta-AnalysisJournal of Cancer, 2018
- Prognostic significance of circulating soluble programmed death ligand-1 in patients with solid tumorsMedicine, 2018
- Soluble PD-1 and PD-L1: predictive and prognostic significance in cancerOncotarget, 2017
- Biomarkers to predict prognosis and response to checkpoint inhibitorsInternational Journal of Clinical Oncology, 2017
- Biomarkers for the Clinical Use of PD-1/PD-L1 Inhibitors in Non–Small-Cell Lung CancerJAMA Oncology, 2016
- Targeting immune checkpoints in unresectable metastatic cutaneous melanoma: a systematic review and meta‐analysis of anti‐CTLA‐4 and anti‐PD‐1 agents trialsCancer Medicine, 2016
- Prognostic Significance of Programmed Cell Death 1 (PD-1) or PD-1 Ligand 1 (PD-L1) Expression in Epithelial-Originated CancerMedicine, 2015