非小细胞肺癌中PD-L1免疫组化的可比性及其与临床特征的相关性

IF 2.6 4区 医学 Q3 CELL BIOLOGY
Analytical Cellular Pathology Pub Date : 2020-11-02 eCollection Date: 2020-01-01 DOI:10.1155/2020/3286139
Chiao-En Wu, Ching-Fu Chang, Liao Kou-Sheng, Ju Chiang, Shih-Wei Lee, Yu-Chi Chiu
{"title":"非小细胞肺癌中PD-L1免疫组化的可比性及其与临床特征的相关性","authors":"Chiao-En Wu,&nbsp;Ching-Fu Chang,&nbsp;Liao Kou-Sheng,&nbsp;Ju Chiang,&nbsp;Shih-Wei Lee,&nbsp;Yu-Chi Chiu","doi":"10.1155/2020/3286139","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>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.</p><p><strong>Materials and methods: </strong>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, 8<sup>th</sup> edition), and EGFR/ALK alterations, were analyzed for association with PD-L1 expression.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":49326,"journal":{"name":"Analytical Cellular Pathology","volume":"2020 ","pages":"3286139"},"PeriodicalIF":2.6000,"publicationDate":"2020-11-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2020/3286139","citationCount":"3","resultStr":"{\"title\":\"PD-L1 Immunohistochemistry Comparability and Their Correlation with Clinical Characteristics in NSCLC.\",\"authors\":\"Chiao-En Wu,&nbsp;Ching-Fu Chang,&nbsp;Liao Kou-Sheng,&nbsp;Ju Chiang,&nbsp;Shih-Wei Lee,&nbsp;Yu-Chi Chiu\",\"doi\":\"10.1155/2020/3286139\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>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.</p><p><strong>Materials and methods: </strong>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, 8<sup>th</sup> edition), and EGFR/ALK alterations, were analyzed for association with PD-L1 expression.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>\",\"PeriodicalId\":49326,\"journal\":{\"name\":\"Analytical Cellular Pathology\",\"volume\":\"2020 \",\"pages\":\"3286139\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2020-11-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1155/2020/3286139\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Analytical Cellular Pathology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1155/2020/3286139\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2020/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q3\",\"JCRName\":\"CELL BIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Cellular Pathology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1155/2020/3286139","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2020/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"CELL BIOLOGY","Score":null,"Total":0}
引用次数: 3

摘要

背景:PD-L1表达是免疫检查点抑制剂(ICIs)治疗反应的重要预测因素。本研究旨在回顾性分析三种不同检测方法(Dako22C3、Dako28-8和SP142)在非小细胞肺癌患者中PD-L1测量的一致性,并寻找PD-L1高表达的可能预测因素。材料与方法:回顾性分析桃园总医院2018 - 2019年收治的144例经组织学证实的非小细胞肺癌患者的PD-L1测量数据。分析患者的特征,包括年龄、性别、非小细胞肺癌(AJCC,第8版)的临床分期(T、N、M)和EGFR/ALK改变与PD-L1表达的关系。结果:测定Dako22C3和Dako28-8的PD-L1表达水平具有可比性,而SP142的PD-L1表达水平较低。Dako22C3和Dako28-8在1%和50% TPS临界值上的总体一致性分别为82.2%和91.6%。Cohen的kappa证实了上述发现。此外,我们发现PD-L1表达与晚期N期显著相关,而与T和M期无关。结论:Dako22C3和Dako28-8在评估PD-L1水平方面具有可比性。需要进一步的前瞻性研究来验证这些发现。N分期可能是PD-L1表达的良好预测因子。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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

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

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 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.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Analytical Cellular Pathology
Analytical Cellular Pathology ONCOLOGY-CELL BIOLOGY
CiteScore
4.90
自引率
3.10%
发文量
70
审稿时长
16 weeks
期刊介绍: Analytical Cellular Pathology is a peer-reviewed, Open Access journal that provides a forum for scientists, medical practitioners and pathologists working in the area of cellular pathology. The journal publishes original research articles, review articles, and clinical studies related to cytology, carcinogenesis, cell receptors, biomarkers, diagnostic pathology, immunopathology, and hematology.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信