Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma

Autores
García, Alejandro; Recondo, Gonzalo; Greco, Martín; de la Vega, Máximo; Perazzo, Florencia; Avagnina, Alejandra; Denninghoff, Valeria Cecilia
Año de publicación
2020
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
Lung cancer is the leading cause of cancer-related death worldwide. Recent advances in the management of non-small cell carcinoma are focused on the discovery of targeted therapies and novel immunotherapy strategies for patients with advanced disease. Treatment with anti PD-(L)1 immune checkpoint inhibitors requires the development of predictive biomarkers to select those patients that can most benefit from these therapies. Several immunohistochemical biomarkers have been developed in different technological platforms. However, the most useful and accessible for the daily clinical practice need to be selected. The objective of this study was to compare PD-L1 expression by automated immunohistochemistry in lung adenocarcinoma (ADC) FFPE samples with clones 28-8 and SP263 performed with the BenchMark GX automated staining instrument. To further determine interobserver agreement between two pathologists, and to correlate the results with histologic and pathology variables. FFPE tissue from 40 samples obtained from patients with lung ADC were reviewed retrospectively. Among all studied specimens, 53% of samples presented <1% of positive tumor cells with the 28-8 clone and 50% had <1% of PD-L1 expression in tumor cells with the SP263 clone; PD-L1 expression between ≥1 and <5% was observed in 18% and 24%; ≥5 and <50% PD-L1 expression in 18% and 21%; and ≥50% PD-L1 expression in 11% and 5% of samples, respectively. Similar results between antibodies were observed in 84% of cases for each of the four PD-L1 cutoff groups (Pearson's score 0.90, p < 0.00001). The interobserver degree of agreement calculated with Kappa was 0.75 (95%CI: 0.57–0.93), z = 7.08; p < 0.001. Lepidic, acinar and mucinous patterns had predominantly <1% PD-L1 expression, and the solid pattern subtype had high levels of PD-L1 staining using both clones. PD-L1 expression in less than 1% of tumor cells was similar in stages I/II compared to III/IV. No significant differences were observed in PD-L1 staining and quantification pattern between IHC antibodies 28-8 and SP263.
Fil: García, Alejandro. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; Argentina
Fil: Recondo, Gonzalo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET; Argentina
Fil: Greco, Martín. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; Argentina
Fil: de la Vega, Máximo. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; Argentina
Fil: Perazzo, Florencia. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; Argentina
Fil: Avagnina, Alejandra. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; Argentina
Fil: Denninghoff, Valeria Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET; Argentina
Materia
28-8
BIOMARKERS
DIAGNOSTICS
HISTOPATHOLOGY
IMMUNOLOGY
LUNG ADENOCARCINOMA
ONCOLOGY
PATHOLOGY
PD-L1
SP263
Nivel de accesibilidad
acceso abierto
Condiciones de uso
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
Repositorio
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
oai:ri.conicet.gov.ar:11336/145938

id CONICETDig_d5aab7053f90b275c17e1e72cbe8358c
oai_identifier_str oai:ri.conicet.gov.ar:11336/145938
network_acronym_str CONICETDig
repository_id_str 3498
network_name_str CONICET Digital (CONICET)
spelling Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinomaGarcía, AlejandroRecondo, GonzaloGreco, Martínde la Vega, MáximoPerazzo, FlorenciaAvagnina, AlejandraDenninghoff, Valeria Cecilia28-8BIOMARKERSDIAGNOSTICSHISTOPATHOLOGYIMMUNOLOGYLUNG ADENOCARCINOMAONCOLOGYPATHOLOGYPD-L1SP263https://purl.org/becyt/ford/3.2https://purl.org/becyt/ford/3Lung cancer is the leading cause of cancer-related death worldwide. Recent advances in the management of non-small cell carcinoma are focused on the discovery of targeted therapies and novel immunotherapy strategies for patients with advanced disease. Treatment with anti PD-(L)1 immune checkpoint inhibitors requires the development of predictive biomarkers to select those patients that can most benefit from these therapies. Several immunohistochemical biomarkers have been developed in different technological platforms. However, the most useful and accessible for the daily clinical practice need to be selected. The objective of this study was to compare PD-L1 expression by automated immunohistochemistry in lung adenocarcinoma (ADC) FFPE samples with clones 28-8 and SP263 performed with the BenchMark GX automated staining instrument. To further determine interobserver agreement between two pathologists, and to correlate the results with histologic and pathology variables. FFPE tissue from 40 samples obtained from patients with lung ADC were reviewed retrospectively. Among all studied specimens, 53% of samples presented <1% of positive tumor cells with the 28-8 clone and 50% had <1% of PD-L1 expression in tumor cells with the SP263 clone; PD-L1 expression between ≥1 and <5% was observed in 18% and 24%; ≥5 and <50% PD-L1 expression in 18% and 21%; and ≥50% PD-L1 expression in 11% and 5% of samples, respectively. Similar results between antibodies were observed in 84% of cases for each of the four PD-L1 cutoff groups (Pearson's score 0.90, p < 0.00001). The interobserver degree of agreement calculated with Kappa was 0.75 (95%CI: 0.57–0.93), z = 7.08; p < 0.001. Lepidic, acinar and mucinous patterns had predominantly <1% PD-L1 expression, and the solid pattern subtype had high levels of PD-L1 staining using both clones. PD-L1 expression in less than 1% of tumor cells was similar in stages I/II compared to III/IV. No significant differences were observed in PD-L1 staining and quantification pattern between IHC antibodies 28-8 and SP263.Fil: García, Alejandro. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; ArgentinaFil: Recondo, Gonzalo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET; ArgentinaFil: Greco, Martín. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; ArgentinaFil: de la Vega, Máximo. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; ArgentinaFil: Perazzo, Florencia. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; ArgentinaFil: Avagnina, Alejandra. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; ArgentinaFil: Denninghoff, Valeria Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET; ArgentinaElsevier2020-06info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/145938García, Alejandro; Recondo, Gonzalo; Greco, Martín; de la Vega, Máximo; Perazzo, Florencia; et al.; Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma; Elsevier; Heliyon; 6; 6; 6-2020; 1-42405-8440CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S2405844020309610info:eu-repo/semantics/altIdentifier/doi/10.1016/j.heliyon.2020.e04117info:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-nd/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-10T13:10:33Zoai:ri.conicet.gov.ar:11336/145938instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-09-10 13:10:33.393CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse
dc.title.none.fl_str_mv Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma
title Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma
spellingShingle Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma
García, Alejandro
28-8
BIOMARKERS
DIAGNOSTICS
HISTOPATHOLOGY
IMMUNOLOGY
LUNG ADENOCARCINOMA
ONCOLOGY
PATHOLOGY
PD-L1
SP263
title_short Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma
title_full Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma
title_fullStr Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma
title_full_unstemmed Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma
title_sort Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma
dc.creator.none.fl_str_mv García, Alejandro
Recondo, Gonzalo
Greco, Martín
de la Vega, Máximo
Perazzo, Florencia
Avagnina, Alejandra
Denninghoff, Valeria Cecilia
author García, Alejandro
author_facet García, Alejandro
Recondo, Gonzalo
Greco, Martín
de la Vega, Máximo
Perazzo, Florencia
Avagnina, Alejandra
Denninghoff, Valeria Cecilia
author_role author
author2 Recondo, Gonzalo
Greco, Martín
de la Vega, Máximo
Perazzo, Florencia
Avagnina, Alejandra
Denninghoff, Valeria Cecilia
author2_role author
author
author
author
author
author
dc.subject.none.fl_str_mv 28-8
BIOMARKERS
DIAGNOSTICS
HISTOPATHOLOGY
IMMUNOLOGY
LUNG ADENOCARCINOMA
ONCOLOGY
PATHOLOGY
PD-L1
SP263
topic 28-8
BIOMARKERS
DIAGNOSTICS
HISTOPATHOLOGY
IMMUNOLOGY
LUNG ADENOCARCINOMA
ONCOLOGY
PATHOLOGY
PD-L1
SP263
purl_subject.fl_str_mv https://purl.org/becyt/ford/3.2
https://purl.org/becyt/ford/3
dc.description.none.fl_txt_mv Lung cancer is the leading cause of cancer-related death worldwide. Recent advances in the management of non-small cell carcinoma are focused on the discovery of targeted therapies and novel immunotherapy strategies for patients with advanced disease. Treatment with anti PD-(L)1 immune checkpoint inhibitors requires the development of predictive biomarkers to select those patients that can most benefit from these therapies. Several immunohistochemical biomarkers have been developed in different technological platforms. However, the most useful and accessible for the daily clinical practice need to be selected. The objective of this study was to compare PD-L1 expression by automated immunohistochemistry in lung adenocarcinoma (ADC) FFPE samples with clones 28-8 and SP263 performed with the BenchMark GX automated staining instrument. To further determine interobserver agreement between two pathologists, and to correlate the results with histologic and pathology variables. FFPE tissue from 40 samples obtained from patients with lung ADC were reviewed retrospectively. Among all studied specimens, 53% of samples presented <1% of positive tumor cells with the 28-8 clone and 50% had <1% of PD-L1 expression in tumor cells with the SP263 clone; PD-L1 expression between ≥1 and <5% was observed in 18% and 24%; ≥5 and <50% PD-L1 expression in 18% and 21%; and ≥50% PD-L1 expression in 11% and 5% of samples, respectively. Similar results between antibodies were observed in 84% of cases for each of the four PD-L1 cutoff groups (Pearson's score 0.90, p < 0.00001). The interobserver degree of agreement calculated with Kappa was 0.75 (95%CI: 0.57–0.93), z = 7.08; p < 0.001. Lepidic, acinar and mucinous patterns had predominantly <1% PD-L1 expression, and the solid pattern subtype had high levels of PD-L1 staining using both clones. PD-L1 expression in less than 1% of tumor cells was similar in stages I/II compared to III/IV. No significant differences were observed in PD-L1 staining and quantification pattern between IHC antibodies 28-8 and SP263.
Fil: García, Alejandro. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; Argentina
Fil: Recondo, Gonzalo. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET; Argentina
Fil: Greco, Martín. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; Argentina
Fil: de la Vega, Máximo. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; Argentina
Fil: Perazzo, Florencia. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; Argentina
Fil: Avagnina, Alejandra. Centro de Educación Médica e Investigaciones Clínicas "Norberto Quirno"; Argentina
Fil: Denninghoff, Valeria Cecilia. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. CEMIC-CONICET. Centro de Educaciones Médicas e Investigaciones Clínicas "Norberto Quirno". CEMIC-CONICET; Argentina
description Lung cancer is the leading cause of cancer-related death worldwide. Recent advances in the management of non-small cell carcinoma are focused on the discovery of targeted therapies and novel immunotherapy strategies for patients with advanced disease. Treatment with anti PD-(L)1 immune checkpoint inhibitors requires the development of predictive biomarkers to select those patients that can most benefit from these therapies. Several immunohistochemical biomarkers have been developed in different technological platforms. However, the most useful and accessible for the daily clinical practice need to be selected. The objective of this study was to compare PD-L1 expression by automated immunohistochemistry in lung adenocarcinoma (ADC) FFPE samples with clones 28-8 and SP263 performed with the BenchMark GX automated staining instrument. To further determine interobserver agreement between two pathologists, and to correlate the results with histologic and pathology variables. FFPE tissue from 40 samples obtained from patients with lung ADC were reviewed retrospectively. Among all studied specimens, 53% of samples presented <1% of positive tumor cells with the 28-8 clone and 50% had <1% of PD-L1 expression in tumor cells with the SP263 clone; PD-L1 expression between ≥1 and <5% was observed in 18% and 24%; ≥5 and <50% PD-L1 expression in 18% and 21%; and ≥50% PD-L1 expression in 11% and 5% of samples, respectively. Similar results between antibodies were observed in 84% of cases for each of the four PD-L1 cutoff groups (Pearson's score 0.90, p < 0.00001). The interobserver degree of agreement calculated with Kappa was 0.75 (95%CI: 0.57–0.93), z = 7.08; p < 0.001. Lepidic, acinar and mucinous patterns had predominantly <1% PD-L1 expression, and the solid pattern subtype had high levels of PD-L1 staining using both clones. PD-L1 expression in less than 1% of tumor cells was similar in stages I/II compared to III/IV. No significant differences were observed in PD-L1 staining and quantification pattern between IHC antibodies 28-8 and SP263.
publishDate 2020
dc.date.none.fl_str_mv 2020-06
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
http://purl.org/coar/resource_type/c_6501
info:ar-repo/semantics/articulo
format article
status_str publishedVersion
dc.identifier.none.fl_str_mv http://hdl.handle.net/11336/145938
García, Alejandro; Recondo, Gonzalo; Greco, Martín; de la Vega, Máximo; Perazzo, Florencia; et al.; Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma; Elsevier; Heliyon; 6; 6; 6-2020; 1-4
2405-8440
CONICET Digital
CONICET
url http://hdl.handle.net/11336/145938
identifier_str_mv García, Alejandro; Recondo, Gonzalo; Greco, Martín; de la Vega, Máximo; Perazzo, Florencia; et al.; Correlation between PD-L1 expression (clones 28-8 and SP263) and histopathology in lung adenocarcinoma; Elsevier; Heliyon; 6; 6; 6-2020; 1-4
2405-8440
CONICET Digital
CONICET
dc.language.none.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv info:eu-repo/semantics/altIdentifier/url/https://linkinghub.elsevier.com/retrieve/pii/S2405844020309610
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.heliyon.2020.e04117
dc.rights.none.fl_str_mv info:eu-repo/semantics/openAccess
https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
eu_rights_str_mv openAccess
rights_invalid_str_mv https://creativecommons.org/licenses/by-nc-nd/2.5/ar/
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:CONICET Digital (CONICET)
instname:Consejo Nacional de Investigaciones Científicas y Técnicas
reponame_str CONICET Digital (CONICET)
collection CONICET Digital (CONICET)
instname_str Consejo Nacional de Investigaciones Científicas y Técnicas
repository.name.fl_str_mv CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas
repository.mail.fl_str_mv dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar
_version_ 1842980532008255488
score 12.993085