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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...
Autores principales: | , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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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. |
format | Online Article Text |
id | pubmed-8007750 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
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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