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Response of Patients with Taxane-Refractory Advanced Urothelial Cancer to Enfortumab Vedotin, a Microtubule-Disrupting Agent

Enfortumab vedotin (EV), a nectin-4-directed antibody conjugated to monomethyl auristatin E (MMAE), has been approved for patients with advanced urothelial carcinoma (aUC) previously treated with platinum-based chemotherapy and immune inhibitors. Taxane agents and MMAE share antitumor mechanisms thr...

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Autores principales: Miyake, Makito, Nishimura, Nobutaka, Miyamoto, Tatsuki, Shimizu, Takuto, Ohnishi, Kenta, Hori, Shunta, Morizawa, Yosuke, Gotoh, Daisuke, Nakai, Yasushi, Torimoto, Kazumasa, Fujii, Tomomi, Fujimoto, Kiyohide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867573/
https://www.ncbi.nlm.nih.gov/pubmed/36691441
http://dx.doi.org/10.1155/2023/1024239
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author Miyake, Makito
Nishimura, Nobutaka
Miyamoto, Tatsuki
Shimizu, Takuto
Ohnishi, Kenta
Hori, Shunta
Morizawa, Yosuke
Gotoh, Daisuke
Nakai, Yasushi
Torimoto, Kazumasa
Fujii, Tomomi
Fujimoto, Kiyohide
author_facet Miyake, Makito
Nishimura, Nobutaka
Miyamoto, Tatsuki
Shimizu, Takuto
Ohnishi, Kenta
Hori, Shunta
Morizawa, Yosuke
Gotoh, Daisuke
Nakai, Yasushi
Torimoto, Kazumasa
Fujii, Tomomi
Fujimoto, Kiyohide
author_sort Miyake, Makito
collection PubMed
description Enfortumab vedotin (EV), a nectin-4-directed antibody conjugated to monomethyl auristatin E (MMAE), has been approved for patients with advanced urothelial carcinoma (aUC) previously treated with platinum-based chemotherapy and immune inhibitors. Taxane agents and MMAE share antitumor mechanisms through microtubule disruption, thus raising a notable concern regarding cross-resistance between these drugs. This case report describes two patients with taxane-based chemotherapy-refractory aUC who responded well to EV. A 71-year-old man (case 1) with pT3N0M0 renal pelvic UC showed a partial response to EV in metastatic lesions of the bilateral lungs and right pelvic lymph nodes after three cycles of paclitaxel plus gemcitabine chemotherapy. A 53-year-old man (case 2) with cT3bN2M0 bladder UC underwent platinum-based neoadjuvant chemotherapy and the following radial cystectomy (ypTis ypN0). He developed bilateral lung metastases and showed a complete response to EV in the metastatic lesions after 20 cycles of paclitaxel plus nedaplatin chemotherapy. Our experience of two cases demonstrated that tumor response to EV can be expected in patients with taxane-refractory aUC.
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spelling pubmed-98675732023-01-22 Response of Patients with Taxane-Refractory Advanced Urothelial Cancer to Enfortumab Vedotin, a Microtubule-Disrupting Agent Miyake, Makito Nishimura, Nobutaka Miyamoto, Tatsuki Shimizu, Takuto Ohnishi, Kenta Hori, Shunta Morizawa, Yosuke Gotoh, Daisuke Nakai, Yasushi Torimoto, Kazumasa Fujii, Tomomi Fujimoto, Kiyohide Case Rep Urol Case Report Enfortumab vedotin (EV), a nectin-4-directed antibody conjugated to monomethyl auristatin E (MMAE), has been approved for patients with advanced urothelial carcinoma (aUC) previously treated with platinum-based chemotherapy and immune inhibitors. Taxane agents and MMAE share antitumor mechanisms through microtubule disruption, thus raising a notable concern regarding cross-resistance between these drugs. This case report describes two patients with taxane-based chemotherapy-refractory aUC who responded well to EV. A 71-year-old man (case 1) with pT3N0M0 renal pelvic UC showed a partial response to EV in metastatic lesions of the bilateral lungs and right pelvic lymph nodes after three cycles of paclitaxel plus gemcitabine chemotherapy. A 53-year-old man (case 2) with cT3bN2M0 bladder UC underwent platinum-based neoadjuvant chemotherapy and the following radial cystectomy (ypTis ypN0). He developed bilateral lung metastases and showed a complete response to EV in the metastatic lesions after 20 cycles of paclitaxel plus nedaplatin chemotherapy. Our experience of two cases demonstrated that tumor response to EV can be expected in patients with taxane-refractory aUC. Hindawi 2023-01-14 /pmc/articles/PMC9867573/ /pubmed/36691441 http://dx.doi.org/10.1155/2023/1024239 Text en Copyright © 2023 Makito Miyake et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Miyake, Makito
Nishimura, Nobutaka
Miyamoto, Tatsuki
Shimizu, Takuto
Ohnishi, Kenta
Hori, Shunta
Morizawa, Yosuke
Gotoh, Daisuke
Nakai, Yasushi
Torimoto, Kazumasa
Fujii, Tomomi
Fujimoto, Kiyohide
Response of Patients with Taxane-Refractory Advanced Urothelial Cancer to Enfortumab Vedotin, a Microtubule-Disrupting Agent
title Response of Patients with Taxane-Refractory Advanced Urothelial Cancer to Enfortumab Vedotin, a Microtubule-Disrupting Agent
title_full Response of Patients with Taxane-Refractory Advanced Urothelial Cancer to Enfortumab Vedotin, a Microtubule-Disrupting Agent
title_fullStr Response of Patients with Taxane-Refractory Advanced Urothelial Cancer to Enfortumab Vedotin, a Microtubule-Disrupting Agent
title_full_unstemmed Response of Patients with Taxane-Refractory Advanced Urothelial Cancer to Enfortumab Vedotin, a Microtubule-Disrupting Agent
title_short Response of Patients with Taxane-Refractory Advanced Urothelial Cancer to Enfortumab Vedotin, a Microtubule-Disrupting Agent
title_sort response of patients with taxane-refractory advanced urothelial cancer to enfortumab vedotin, a microtubule-disrupting agent
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9867573/
https://www.ncbi.nlm.nih.gov/pubmed/36691441
http://dx.doi.org/10.1155/2023/1024239
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