PD-L1 Immunohistochemistry Comparability and Their Correlation with Clinical Characteristics in NSCLC

Background. PD-L1 expression is an important predictive factor of response to therapy with immune checkpoint inhibitors (ICIs). This study was designed to retrospectively analyze the concordance of PD-L1 measurements using three different assays (Dako22C3, Dako28-8, and SP142) in NSCLC patients and...

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Main Authors: Chiao-En Wu, Ching-Fu Chang, Liao Kou-Sheng, Ju Chiang, Shih-Wei Lee, Yu-Chi Chiu
Format: Article
Language:English
Published: Wiley 2020-01-01
Series:Analytical Cellular Pathology
Online Access:http://dx.doi.org/10.1155/2020/3286139
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author Chiao-En Wu
Ching-Fu Chang
Liao Kou-Sheng
Ju Chiang
Shih-Wei Lee
Yu-Chi Chiu
author_facet Chiao-En Wu
Ching-Fu Chang
Liao Kou-Sheng
Ju Chiang
Shih-Wei Lee
Yu-Chi Chiu
author_sort Chiao-En Wu
collection DOAJ
description Background. PD-L1 expression is an important predictive factor of response to therapy with immune checkpoint inhibitors (ICIs). This study was designed to retrospectively analyze the concordance of PD-L1 measurements using three different assays (Dako22C3, Dako28-8, and SP142) in NSCLC patients and to find possible predictors of high PD-L1 expression. Materials and Methods. Data of 144 patients with histologically confirmed NSCLC and available PD-L1 measurements treated at the Taoyuan General Hospital from 2018 to 2019 were retrospectively reviewed in the study. Patients’ characteristics, including age, sex, clinical stage (T, N, and M) of NSCLC (AJCC, 8th edition), and EGFR/ALK alterations, were analyzed for association with PD-L1 expression. Results. Measurements of PD-L1 expression levels with Dako22C3 and Dako28-8 were comparable while SP142 showed lower levels of PD-L1 expression. The overall agreement between Dako22C3 and Dako28-8 was 82.2% and 91.6% for both 1% and 50% TPS cut-offs, respectively. The above findings were confirmed by Cohen’s kappa. In addition, we found that PD-L1 expression was significantly associated with advanced N stage but not with T and M stages. Conclusion. Dako22C3 and Dako28-8 showed comparable results in assessing PD-L1 levels. Future prospective studies are needed to validate these findings. N stage may be a good predictor for PD-L1 expression.
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spelling doaj-art-28ba5343ed1047a58a1ba37da04a57df2025-02-03T06:45:50ZengWileyAnalytical Cellular Pathology2210-71772210-71852020-01-01202010.1155/2020/32861393286139PD-L1 Immunohistochemistry Comparability and Their Correlation with Clinical Characteristics in NSCLCChiao-En Wu0Ching-Fu Chang1Liao Kou-Sheng2Ju Chiang3Shih-Wei Lee4Yu-Chi Chiu5Division of Haematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, TaiwanDivision of Haematology-Oncology, Department of Internal Medicine, Chang Gung Memorial Hospital at Linkou, Chang Gung University College of Medicine, Taoyuan, TaiwanDepartment of Pathology, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan, TaiwanDepartment of Internal Medicine, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan, TaiwanDepartment of Internal Medicine, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan, TaiwanDepartment of Internal Medicine, Taoyuan General Hospital, Ministry of Health and Welfare, Taoyuan, TaiwanBackground. PD-L1 expression is an important predictive factor of response to therapy with immune checkpoint inhibitors (ICIs). This study was designed to retrospectively analyze the concordance of PD-L1 measurements using three different assays (Dako22C3, Dako28-8, and SP142) in NSCLC patients and to find possible predictors of high PD-L1 expression. Materials and Methods. Data of 144 patients with histologically confirmed NSCLC and available PD-L1 measurements treated at the Taoyuan General Hospital from 2018 to 2019 were retrospectively reviewed in the study. Patients’ characteristics, including age, sex, clinical stage (T, N, and M) of NSCLC (AJCC, 8th edition), and EGFR/ALK alterations, were analyzed for association with PD-L1 expression. Results. Measurements of PD-L1 expression levels with Dako22C3 and Dako28-8 were comparable while SP142 showed lower levels of PD-L1 expression. The overall agreement between Dako22C3 and Dako28-8 was 82.2% and 91.6% for both 1% and 50% TPS cut-offs, respectively. The above findings were confirmed by Cohen’s kappa. In addition, we found that PD-L1 expression was significantly associated with advanced N stage but not with T and M stages. Conclusion. Dako22C3 and Dako28-8 showed comparable results in assessing PD-L1 levels. Future prospective studies are needed to validate these findings. N stage may be a good predictor for PD-L1 expression.http://dx.doi.org/10.1155/2020/3286139
spellingShingle Chiao-En Wu
Ching-Fu Chang
Liao Kou-Sheng
Ju Chiang
Shih-Wei Lee
Yu-Chi Chiu
PD-L1 Immunohistochemistry Comparability and Their Correlation with Clinical Characteristics in NSCLC
Analytical Cellular Pathology
title PD-L1 Immunohistochemistry Comparability and Their Correlation with Clinical Characteristics in NSCLC
title_full PD-L1 Immunohistochemistry Comparability and Their Correlation with Clinical Characteristics in NSCLC
title_fullStr PD-L1 Immunohistochemistry Comparability and Their Correlation with Clinical Characteristics in NSCLC
title_full_unstemmed PD-L1 Immunohistochemistry Comparability and Their Correlation with Clinical Characteristics in NSCLC
title_short PD-L1 Immunohistochemistry Comparability and Their Correlation with Clinical Characteristics in NSCLC
title_sort pd l1 immunohistochemistry comparability and their correlation with clinical characteristics in nsclc
url http://dx.doi.org/10.1155/2020/3286139
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