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Current Medical Imaging

Editor-in-Chief

ISSN (Print): 1573-4056
ISSN (Online): 1875-6603

Research Article

Relationship with Programmed Cell Death Ligand 1 (PD-L1) and DTI Features in Brain Metastases of Non-small Cell Lung Cancer: A Preliminary Study

Author(s): Temel Fatih Yilmaz*, Ismail Yurtsever, Hacı Mehmet Turk, Mehmet Ali Gultekin, Mehmet Besiroglu, Dilek Hacer Cesme, Abdallah T M Shbair and Alpay Alkan

Volume 17, Issue 11, 2021

Published on: 17 February, 2021

Page: [1369 - 1373] Pages: 5

DOI: 10.2174/1573405617666210218095953

Price: $65

Abstract

Objective: The purpose of the study was to determine DTI properties of brain metastases in subjects with Non-Small Cell Lung Carcinoma (NSCLC) to evaluate whether there was a correlation between DTI findings and Programmed Cell Death Ligand-1 (PD-L1).

Methods: The study population (n:22) was assigned to PD-L1 negative (Group 1: PD-L1 expression<% 50) (n=11) or positive (Group 2: PD-L1 expression ≥%50) (n=11). We compared ADC and FA values measured from the enhanced solid metastases and peritumoral edema area with PD-L1 protein status.

Results: The mean ADC values were lower in group 2 compared to group 1. The peritumoral ADC values were higher in group 2 compared to group 1. Mean peritumoral edema FA values were lower in group 2 compared to group 1. The peritumoral edema nADC values were higher in group 2 compared to group 1. As PD-L1 expression frequency increased, ADC values in the peritumoral edema area increased and FA values decreased.

Conclusion: We thought that the existence of PD-L1 protein does not affect ADC and FA values of brain metastasis (BM) originating from NSCLC. DTI characteristics of the peritumoral edema area could be a guide in determining the PD-L1 protein status of brain metastases of NSCLC. The relationship between PD-L1 expression status and DTI features in BM from NSCLC could help us to have an idea regarding the response to immunotherapy.

Keywords: Programmed cell death ligand 1, diffusion tensor imaging, brain metastasis, non-small cell lung, immunotherapy, apparent diffusion coefficient.

Graphical Abstract

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