Cargando…

PD-L2 amplification and durable disease stabilization in patient with urothelial carcinoma receiving pembrolizumab

We report the immunological profile of a patient with upper-tract urothelial carcinoma experiencing stable disease on pembrolizumab for 20 months. The tumor exhibited extensive infiltration by CD8(+) cytotoxic T lymphocytes, low-to-moderate mutational burden, no PD-L1 staining by commercially availa...

Descripción completa

Detalles Bibliográficos
Autores principales: George, Saby, Papanicolau-Sengos, Antonios, Lenzo, Felicia L., Conroy, Jeffrey M., Nesline, Mary, Pabla, Sarabjot, Glenn, Sean T., Burgher, Blake, Andreas, Jonathan, Giamo, Vincent, Qin, Moachun, Wang, Yirong, Galluzzi, Lorenzo, Morrison, Carl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279415/
https://www.ncbi.nlm.nih.gov/pubmed/30524881
http://dx.doi.org/10.1080/2162402X.2018.1460298
_version_ 1783378502465093632
author George, Saby
Papanicolau-Sengos, Antonios
Lenzo, Felicia L.
Conroy, Jeffrey M.
Nesline, Mary
Pabla, Sarabjot
Glenn, Sean T.
Burgher, Blake
Andreas, Jonathan
Giamo, Vincent
Qin, Moachun
Wang, Yirong
Galluzzi, Lorenzo
Morrison, Carl
author_facet George, Saby
Papanicolau-Sengos, Antonios
Lenzo, Felicia L.
Conroy, Jeffrey M.
Nesline, Mary
Pabla, Sarabjot
Glenn, Sean T.
Burgher, Blake
Andreas, Jonathan
Giamo, Vincent
Qin, Moachun
Wang, Yirong
Galluzzi, Lorenzo
Morrison, Carl
author_sort George, Saby
collection PubMed
description We report the immunological profile of a patient with upper-tract urothelial carcinoma experiencing stable disease on pembrolizumab for 20 months. The tumor exhibited extensive infiltration by CD8(+) cytotoxic T lymphocytes, low-to-moderate mutational burden, no PD-L1 staining by commercially available immunohistochemical assays, but amplification of CD274 (coding for PD-L1) and/or PDCD1LG2 (encoding PD-L2) by fluorescence in situ hybridization. RNA-seq revealed multiple biomarkers of an ongoing immune response and compensatory immune evasion, including moderate PD-L1 levels coupled with robust PD-L2 expression. Pending validation in additional patients, these findings suggest that PD-L2 expression levels may constitute a biomarker of response to immune checkpoint blockade in urothelial carcinoma.
format Online
Article
Text
id pubmed-6279415
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher Taylor & Francis
record_format MEDLINE/PubMed
spelling pubmed-62794152018-12-06 PD-L2 amplification and durable disease stabilization in patient with urothelial carcinoma receiving pembrolizumab George, Saby Papanicolau-Sengos, Antonios Lenzo, Felicia L. Conroy, Jeffrey M. Nesline, Mary Pabla, Sarabjot Glenn, Sean T. Burgher, Blake Andreas, Jonathan Giamo, Vincent Qin, Moachun Wang, Yirong Galluzzi, Lorenzo Morrison, Carl Oncoimmunology Brief Report We report the immunological profile of a patient with upper-tract urothelial carcinoma experiencing stable disease on pembrolizumab for 20 months. The tumor exhibited extensive infiltration by CD8(+) cytotoxic T lymphocytes, low-to-moderate mutational burden, no PD-L1 staining by commercially available immunohistochemical assays, but amplification of CD274 (coding for PD-L1) and/or PDCD1LG2 (encoding PD-L2) by fluorescence in situ hybridization. RNA-seq revealed multiple biomarkers of an ongoing immune response and compensatory immune evasion, including moderate PD-L1 levels coupled with robust PD-L2 expression. Pending validation in additional patients, these findings suggest that PD-L2 expression levels may constitute a biomarker of response to immune checkpoint blockade in urothelial carcinoma. Taylor & Francis 2018-05-29 /pmc/articles/PMC6279415/ /pubmed/30524881 http://dx.doi.org/10.1080/2162402X.2018.1460298 Text en © 2018 The Author(s). Published with license by Taylor & Francis Group, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way.
spellingShingle Brief Report
George, Saby
Papanicolau-Sengos, Antonios
Lenzo, Felicia L.
Conroy, Jeffrey M.
Nesline, Mary
Pabla, Sarabjot
Glenn, Sean T.
Burgher, Blake
Andreas, Jonathan
Giamo, Vincent
Qin, Moachun
Wang, Yirong
Galluzzi, Lorenzo
Morrison, Carl
PD-L2 amplification and durable disease stabilization in patient with urothelial carcinoma receiving pembrolizumab
title PD-L2 amplification and durable disease stabilization in patient with urothelial carcinoma receiving pembrolizumab
title_full PD-L2 amplification and durable disease stabilization in patient with urothelial carcinoma receiving pembrolizumab
title_fullStr PD-L2 amplification and durable disease stabilization in patient with urothelial carcinoma receiving pembrolizumab
title_full_unstemmed PD-L2 amplification and durable disease stabilization in patient with urothelial carcinoma receiving pembrolizumab
title_short PD-L2 amplification and durable disease stabilization in patient with urothelial carcinoma receiving pembrolizumab
title_sort pd-l2 amplification and durable disease stabilization in patient with urothelial carcinoma receiving pembrolizumab
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6279415/
https://www.ncbi.nlm.nih.gov/pubmed/30524881
http://dx.doi.org/10.1080/2162402X.2018.1460298
work_keys_str_mv AT georgesaby pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT papanicolausengosantonios pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT lenzofelicial pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT conroyjeffreym pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT neslinemary pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT pablasarabjot pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT glennseant pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT burgherblake pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT andreasjonathan pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT giamovincent pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT qinmoachun pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT wangyirong pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT galluzzilorenzo pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab
AT morrisoncarl pdl2amplificationanddurablediseasestabilizationinpatientwithurothelialcarcinomareceivingpembrolizumab