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Natural history, response to systemic therapy, and genomic landscape of plasmacytoid urothelial carcinoma

BACKGROUND: Plasmacytoid urothelial carcinoma (PUC) is a rare, aggressive histologic variant of urothelial cancer characterised by a diffuse growth pattern and CDH1 mutation. We studied the efficacy of preoperative platinum-based chemotherapy in nonmetastatic PUC and immune checkpoint inhibitors (IC...

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Autores principales: Teo, Min Yuen, Al-Ahmadie, Hikmat, Seier, Kenneth, Tully, Christopher, Regazzi, Ashley M., Pietzak, Eugene, Solit, David B., Tickoo, Satish, Reuter, Victor, Cha, Eugene K., Herr, Harry, Donahue, Timothy, Donat, Sherri M., Dalbagni, Guido, Bochner, Bernard H., Funt, Samuel, Iyer, Gopakumar V., Bajorin, Dean F., Ostrovnaya, Irina, Rosenberg, Jonathan E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007750/
https://www.ncbi.nlm.nih.gov/pubmed/33473164
http://dx.doi.org/10.1038/s41416-020-01244-2
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author Teo, Min Yuen
Al-Ahmadie, Hikmat
Seier, Kenneth
Tully, Christopher
Regazzi, Ashley M.
Pietzak, Eugene
Solit, David B.
Tickoo, Satish
Reuter, Victor
Cha, Eugene K.
Herr, Harry
Donahue, Timothy
Donat, Sherri M.
Dalbagni, Guido
Bochner, Bernard H.
Funt, Samuel
Iyer, Gopakumar V.
Bajorin, Dean F.
Ostrovnaya, Irina
Rosenberg, Jonathan E.
author_facet Teo, Min Yuen
Al-Ahmadie, Hikmat
Seier, Kenneth
Tully, Christopher
Regazzi, Ashley M.
Pietzak, Eugene
Solit, David B.
Tickoo, Satish
Reuter, Victor
Cha, Eugene K.
Herr, Harry
Donahue, Timothy
Donat, Sherri M.
Dalbagni, Guido
Bochner, Bernard H.
Funt, Samuel
Iyer, Gopakumar V.
Bajorin, Dean F.
Ostrovnaya, Irina
Rosenberg, Jonathan E.
author_sort Teo, Min Yuen
collection PubMed
description BACKGROUND: Plasmacytoid urothelial carcinoma (PUC) is a rare, aggressive histologic variant of urothelial cancer characterised by a diffuse growth pattern and CDH1 mutation. We studied the efficacy of preoperative platinum-based chemotherapy in nonmetastatic PUC and immune checkpoint inhibitors (ICIs) in advanced PUC. METHODS: Cases of nonmetastatic PUC and advanced PUC treated with ICIs at our institution were identified. Outcomes were compared to those of a published cohort of patients with urothelial carcinoma not otherwise specified. RESULTS: We identified 81 patients with nonmetastatic PUC. Of the patients with localised disease who underwent neoadjuvant chemotherapy, pathologic complete response and downstaging rates were 12 and 21%, respectively. Pathologic downstaging was not associated with significant improvement in clinical outcomes. Up to 18% of localised disease and 28% of locally advanced cases had unresectable disease at the time of surgery. ICI-treated advanced PUC (N = 21) had progression-free and overall survival of 4.5 and 10.5 months, respectively, and a 38% response rate. FGFR3 and DNA damage response gene alterations were observed in 3 and 15% of cases, respectively. CONCLUSIONS: PUC is associated with high disease burden and poor chemosensitivity. Increased awareness and recognition of this disease variant will allow for new treatment strategies.
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spelling pubmed-80077502022-01-21 Natural history, response to systemic therapy, and genomic landscape of plasmacytoid urothelial carcinoma Teo, Min Yuen Al-Ahmadie, Hikmat Seier, Kenneth Tully, Christopher Regazzi, Ashley M. Pietzak, Eugene Solit, David B. Tickoo, Satish Reuter, Victor Cha, Eugene K. Herr, Harry Donahue, Timothy Donat, Sherri M. Dalbagni, Guido Bochner, Bernard H. Funt, Samuel Iyer, Gopakumar V. Bajorin, Dean F. Ostrovnaya, Irina Rosenberg, Jonathan E. Br J Cancer Article BACKGROUND: Plasmacytoid urothelial carcinoma (PUC) is a rare, aggressive histologic variant of urothelial cancer characterised by a diffuse growth pattern and CDH1 mutation. We studied the efficacy of preoperative platinum-based chemotherapy in nonmetastatic PUC and immune checkpoint inhibitors (ICIs) in advanced PUC. METHODS: Cases of nonmetastatic PUC and advanced PUC treated with ICIs at our institution were identified. Outcomes were compared to those of a published cohort of patients with urothelial carcinoma not otherwise specified. RESULTS: We identified 81 patients with nonmetastatic PUC. Of the patients with localised disease who underwent neoadjuvant chemotherapy, pathologic complete response and downstaging rates were 12 and 21%, respectively. Pathologic downstaging was not associated with significant improvement in clinical outcomes. Up to 18% of localised disease and 28% of locally advanced cases had unresectable disease at the time of surgery. ICI-treated advanced PUC (N = 21) had progression-free and overall survival of 4.5 and 10.5 months, respectively, and a 38% response rate. FGFR3 and DNA damage response gene alterations were observed in 3 and 15% of cases, respectively. CONCLUSIONS: PUC is associated with high disease burden and poor chemosensitivity. Increased awareness and recognition of this disease variant will allow for new treatment strategies. Nature Publishing Group UK 2021-01-21 2021-03-30 /pmc/articles/PMC8007750/ /pubmed/33473164 http://dx.doi.org/10.1038/s41416-020-01244-2 Text en © The Author(s), under exclusive licence to The Author(s), under exclusive licence to Cancer Research UK 2021 https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Teo, Min Yuen
Al-Ahmadie, Hikmat
Seier, Kenneth
Tully, Christopher
Regazzi, Ashley M.
Pietzak, Eugene
Solit, David B.
Tickoo, Satish
Reuter, Victor
Cha, Eugene K.
Herr, Harry
Donahue, Timothy
Donat, Sherri M.
Dalbagni, Guido
Bochner, Bernard H.
Funt, Samuel
Iyer, Gopakumar V.
Bajorin, Dean F.
Ostrovnaya, Irina
Rosenberg, Jonathan E.
Natural history, response to systemic therapy, and genomic landscape of plasmacytoid urothelial carcinoma
title Natural history, response to systemic therapy, and genomic landscape of plasmacytoid urothelial carcinoma
title_full Natural history, response to systemic therapy, and genomic landscape of plasmacytoid urothelial carcinoma
title_fullStr Natural history, response to systemic therapy, and genomic landscape of plasmacytoid urothelial carcinoma
title_full_unstemmed Natural history, response to systemic therapy, and genomic landscape of plasmacytoid urothelial carcinoma
title_short Natural history, response to systemic therapy, and genomic landscape of plasmacytoid urothelial carcinoma
title_sort natural history, response to systemic therapy, and genomic landscape of plasmacytoid urothelial carcinoma
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8007750/
https://www.ncbi.nlm.nih.gov/pubmed/33473164
http://dx.doi.org/10.1038/s41416-020-01244-2
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