Cargando…

Programmed Cell Death-Ligand 1 Expression Status in Urothelial Carcinoma According to Clinical and Pathological Factors: A Multi-Institutional Retrospective Study

Purpose: To investigate programmed cell death-ligand 1 (PD-L1) expression status and the clinical and pathological factors related to its expression in urothelial carcinoma (UC) patients. Materials and Methods: Data from 761 UC patients who underwent testing for PD-L1 expression using the VENTANA (S...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Hyung Suk, Jang, Won Sik, Ham, Won Sik, Jung, Seung Il, Lee, Dong Hyun, Ku, Ja Hyeon, Ha, Hong Koo, Ku, Ja Yoon, Choi, Se Young, Chang, In Ho, Choi, Taesoo, Song, Wan, Jeon, Seong Soo, Jeong, Byong Chang, Kim, Sung Han, Seo, Ho Kyung
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562813/
https://www.ncbi.nlm.nih.gov/pubmed/33134169
http://dx.doi.org/10.3389/fonc.2020.568809
_version_ 1783595353615892480
author Kim, Hyung Suk
Jang, Won Sik
Ham, Won Sik
Jung, Seung Il
Lee, Dong Hyun
Ku, Ja Hyeon
Ha, Hong Koo
Ku, Ja Yoon
Choi, Se Young
Chang, In Ho
Choi, Taesoo
Song, Wan
Jeon, Seong Soo
Jeong, Byong Chang
Kim, Sung Han
Seo, Ho Kyung
author_facet Kim, Hyung Suk
Jang, Won Sik
Ham, Won Sik
Jung, Seung Il
Lee, Dong Hyun
Ku, Ja Hyeon
Ha, Hong Koo
Ku, Ja Yoon
Choi, Se Young
Chang, In Ho
Choi, Taesoo
Song, Wan
Jeon, Seong Soo
Jeong, Byong Chang
Kim, Sung Han
Seo, Ho Kyung
author_sort Kim, Hyung Suk
collection PubMed
description Purpose: To investigate programmed cell death-ligand 1 (PD-L1) expression status and the clinical and pathological factors related to its expression in urothelial carcinoma (UC) patients. Materials and Methods: Data from 761 UC patients who underwent testing for PD-L1 expression using the VENTANA (SP-142 immunohistochemistry assay) for measuring PD-L1 expression according to the manufacturer's protocol between February 2016 and July 2019 were retrospectively reviewed. Patients were categorized into three groups based on the percentage of tumor area covered by PD-L1-expressing tumor-infiltrating immune cells (ICs) as follows: IC0 (<1%), IC1 (≥1% and <5%), and IC2/3 (≥5%). Positive PD-L1 expression was defined as IC2/3 (≥5%). The factors related to positive PD-L1 expression were assessed by using unadjusted and adjusted logistic regression analyses. Results: In the entire cohort, 213 (28%) patients showed positive PD-L1 expression. Final adjusted regression analyses for positive PD-L1 expression revealed that several factors, including intravesical BCG prior to PD-L1 testing (odds ratio [OR] 0.57, 95% confidence interval [CI] 0.37–0.96), advanced tumor stage (stage III/IV) (OR 2.04, 95% CI 1.41–2.93), and high tumor grade (OR 5.31, 95% CI 2.38–11.83) were significantly associated with positive PD-L1 expression. Conclusions: This study showed that the PD-L1 expression is associated with several clinical and pathological factors for the first time in a real-world setting. Further follow-up clinical trials should consider adjusting these factors, including intravesical BCG treatment, tumor stage and grade to clarify the utility of PD-L1 as a biomarker.
format Online
Article
Text
id pubmed-7562813
institution National Center for Biotechnology Information
language English
publishDate 2020
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-75628132020-10-29 Programmed Cell Death-Ligand 1 Expression Status in Urothelial Carcinoma According to Clinical and Pathological Factors: A Multi-Institutional Retrospective Study Kim, Hyung Suk Jang, Won Sik Ham, Won Sik Jung, Seung Il Lee, Dong Hyun Ku, Ja Hyeon Ha, Hong Koo Ku, Ja Yoon Choi, Se Young Chang, In Ho Choi, Taesoo Song, Wan Jeon, Seong Soo Jeong, Byong Chang Kim, Sung Han Seo, Ho Kyung Front Oncol Oncology Purpose: To investigate programmed cell death-ligand 1 (PD-L1) expression status and the clinical and pathological factors related to its expression in urothelial carcinoma (UC) patients. Materials and Methods: Data from 761 UC patients who underwent testing for PD-L1 expression using the VENTANA (SP-142 immunohistochemistry assay) for measuring PD-L1 expression according to the manufacturer's protocol between February 2016 and July 2019 were retrospectively reviewed. Patients were categorized into three groups based on the percentage of tumor area covered by PD-L1-expressing tumor-infiltrating immune cells (ICs) as follows: IC0 (<1%), IC1 (≥1% and <5%), and IC2/3 (≥5%). Positive PD-L1 expression was defined as IC2/3 (≥5%). The factors related to positive PD-L1 expression were assessed by using unadjusted and adjusted logistic regression analyses. Results: In the entire cohort, 213 (28%) patients showed positive PD-L1 expression. Final adjusted regression analyses for positive PD-L1 expression revealed that several factors, including intravesical BCG prior to PD-L1 testing (odds ratio [OR] 0.57, 95% confidence interval [CI] 0.37–0.96), advanced tumor stage (stage III/IV) (OR 2.04, 95% CI 1.41–2.93), and high tumor grade (OR 5.31, 95% CI 2.38–11.83) were significantly associated with positive PD-L1 expression. Conclusions: This study showed that the PD-L1 expression is associated with several clinical and pathological factors for the first time in a real-world setting. Further follow-up clinical trials should consider adjusting these factors, including intravesical BCG treatment, tumor stage and grade to clarify the utility of PD-L1 as a biomarker. Frontiers Media S.A. 2020-10-02 /pmc/articles/PMC7562813/ /pubmed/33134169 http://dx.doi.org/10.3389/fonc.2020.568809 Text en Copyright © 2020 Kim, Jang, Ham, Jung, Lee, Ku, Ha, Ku, Choi, Chang, Choi, Song, Jeon, Jeong, Kim and Seo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Oncology
Kim, Hyung Suk
Jang, Won Sik
Ham, Won Sik
Jung, Seung Il
Lee, Dong Hyun
Ku, Ja Hyeon
Ha, Hong Koo
Ku, Ja Yoon
Choi, Se Young
Chang, In Ho
Choi, Taesoo
Song, Wan
Jeon, Seong Soo
Jeong, Byong Chang
Kim, Sung Han
Seo, Ho Kyung
Programmed Cell Death-Ligand 1 Expression Status in Urothelial Carcinoma According to Clinical and Pathological Factors: A Multi-Institutional Retrospective Study
title Programmed Cell Death-Ligand 1 Expression Status in Urothelial Carcinoma According to Clinical and Pathological Factors: A Multi-Institutional Retrospective Study
title_full Programmed Cell Death-Ligand 1 Expression Status in Urothelial Carcinoma According to Clinical and Pathological Factors: A Multi-Institutional Retrospective Study
title_fullStr Programmed Cell Death-Ligand 1 Expression Status in Urothelial Carcinoma According to Clinical and Pathological Factors: A Multi-Institutional Retrospective Study
title_full_unstemmed Programmed Cell Death-Ligand 1 Expression Status in Urothelial Carcinoma According to Clinical and Pathological Factors: A Multi-Institutional Retrospective Study
title_short Programmed Cell Death-Ligand 1 Expression Status in Urothelial Carcinoma According to Clinical and Pathological Factors: A Multi-Institutional Retrospective Study
title_sort programmed cell death-ligand 1 expression status in urothelial carcinoma according to clinical and pathological factors: a multi-institutional retrospective study
topic Oncology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7562813/
https://www.ncbi.nlm.nih.gov/pubmed/33134169
http://dx.doi.org/10.3389/fonc.2020.568809
work_keys_str_mv AT kimhyungsuk programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT jangwonsik programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT hamwonsik programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT jungseungil programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT leedonghyun programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT kujahyeon programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT hahongkoo programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT kujayoon programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT choiseyoung programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT changinho programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT choitaesoo programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT songwan programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT jeonseongsoo programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT jeongbyongchang programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT kimsunghan programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy
AT seohokyung programmedcelldeathligand1expressionstatusinurothelialcarcinomaaccordingtoclinicalandpathologicalfactorsamultiinstitutionalretrospectivestudy