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Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer

BACKGROUND: Immunotherapies targeting the PD-1 checkpoint pathway have recently gained regulatory approval in numerous cancer types. With the widespread use of immune checkpoint therapies, varying patterns of responses and immune-related adverse events are being observed. CASE PRESENTATION: In this...

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Autores principales: Sweis, Randy F., Zha, Yuanyuan, Pass, Lomax, Heiss, Brian, Chongsuwat, Tara, Luke, Jason J., Gajewski, Thomas F., Szmulewitz, Russell
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883337/
https://www.ncbi.nlm.nih.gov/pubmed/29618376
http://dx.doi.org/10.1186/s40425-018-0334-x
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author Sweis, Randy F.
Zha, Yuanyuan
Pass, Lomax
Heiss, Brian
Chongsuwat, Tara
Luke, Jason J.
Gajewski, Thomas F.
Szmulewitz, Russell
author_facet Sweis, Randy F.
Zha, Yuanyuan
Pass, Lomax
Heiss, Brian
Chongsuwat, Tara
Luke, Jason J.
Gajewski, Thomas F.
Szmulewitz, Russell
author_sort Sweis, Randy F.
collection PubMed
description BACKGROUND: Immunotherapies targeting the PD-1 checkpoint pathway have recently gained regulatory approval in numerous cancer types. With the widespread use of immune checkpoint therapies, varying patterns of responses and immune-related adverse events are being observed. CASE PRESENTATION: In this case, we highlight a patient who developed recurrent, large-volume ascites, while simultaneously having a 49% reduction in peritoneal tumor lesion size by RECIST criteria. Sampling of the fluid revealed high levels of IL-6 and IL-15. Cytology revealed no malignant cells on 4 separate paracenteses over a period of 6 weeks. Cell counts revealed that 45% of cells were lymphocytes, and further analysis was performed by fluorescence-activated cell sorting (FACS). The majority of lymphocytes were CD8(+), of which 78% were PD-1(+) and 43% were HLA-DR(+) indicating an activated phenotype. CONCLUSIONS: In summary, treatment with anti-PD-1 therapy may result in pseudoprogression manifested by ascitic fluid accumulation due to the influx of activated T cells. Since worsening of ascites is typically associated with disease progression, it is important to consider the possibility of pesudoprogression in such patients undergoing therapy with immune checkpoint inhibitors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40425-018-0334-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-58833372018-04-10 Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer Sweis, Randy F. Zha, Yuanyuan Pass, Lomax Heiss, Brian Chongsuwat, Tara Luke, Jason J. Gajewski, Thomas F. Szmulewitz, Russell J Immunother Cancer Case Report BACKGROUND: Immunotherapies targeting the PD-1 checkpoint pathway have recently gained regulatory approval in numerous cancer types. With the widespread use of immune checkpoint therapies, varying patterns of responses and immune-related adverse events are being observed. CASE PRESENTATION: In this case, we highlight a patient who developed recurrent, large-volume ascites, while simultaneously having a 49% reduction in peritoneal tumor lesion size by RECIST criteria. Sampling of the fluid revealed high levels of IL-6 and IL-15. Cytology revealed no malignant cells on 4 separate paracenteses over a period of 6 weeks. Cell counts revealed that 45% of cells were lymphocytes, and further analysis was performed by fluorescence-activated cell sorting (FACS). The majority of lymphocytes were CD8(+), of which 78% were PD-1(+) and 43% were HLA-DR(+) indicating an activated phenotype. CONCLUSIONS: In summary, treatment with anti-PD-1 therapy may result in pseudoprogression manifested by ascitic fluid accumulation due to the influx of activated T cells. Since worsening of ascites is typically associated with disease progression, it is important to consider the possibility of pesudoprogression in such patients undergoing therapy with immune checkpoint inhibitors. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40425-018-0334-x) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-04 /pmc/articles/PMC5883337/ /pubmed/29618376 http://dx.doi.org/10.1186/s40425-018-0334-x Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Case Report
Sweis, Randy F.
Zha, Yuanyuan
Pass, Lomax
Heiss, Brian
Chongsuwat, Tara
Luke, Jason J.
Gajewski, Thomas F.
Szmulewitz, Russell
Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer
title Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer
title_full Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer
title_fullStr Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer
title_full_unstemmed Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer
title_short Pseudoprogression manifesting as recurrent ascites with anti-PD-1 immunotherapy in urothelial bladder cancer
title_sort pseudoprogression manifesting as recurrent ascites with anti-pd-1 immunotherapy in urothelial bladder cancer
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5883337/
https://www.ncbi.nlm.nih.gov/pubmed/29618376
http://dx.doi.org/10.1186/s40425-018-0334-x
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