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A nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer
Despite therapeutic advancements, oral cavity squamous cell carcinoma (OCSCC) remains a difficult disease to treat. Systemic platinum-based chemotherapy often leads to dose-limiting toxicity (DLT), affecting quality of life. PRV111 is a nanotechnology-based system for local delivery of cisplatin loa...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Nature Publishing Group UK
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9385702/ https://www.ncbi.nlm.nih.gov/pubmed/35977936 http://dx.doi.org/10.1038/s41467-022-31859-3 |
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author | Goldberg, Manijeh Manzi, Aaron Birdi, Amritpreet Laporte, Brandon Conway, Peter Cantin, Stefanie Mishra, Vasudha Singh, Alka Pearson, Alexander T. Goldberg, Eric R. Goldberger, Sam Flaum, Benjamin Hasina, Rifat London, Nyall R. Gallia, Gary L. Bettegowda, Chetan Young, Simon Sandulache, Vlad Melville, James Shum, Jonathan O’Neill, Sonya E. Aydin, Erkin Zhavoronkov, Alex Vidal, Anxo Soto, Atenea Alonso, Maria Jose Rosenberg, Ari J. Lingen, Mark W. D’Cruz, Anil Agrawal, Nishant Izumchenko, Evgeny |
author_facet | Goldberg, Manijeh Manzi, Aaron Birdi, Amritpreet Laporte, Brandon Conway, Peter Cantin, Stefanie Mishra, Vasudha Singh, Alka Pearson, Alexander T. Goldberg, Eric R. Goldberger, Sam Flaum, Benjamin Hasina, Rifat London, Nyall R. Gallia, Gary L. Bettegowda, Chetan Young, Simon Sandulache, Vlad Melville, James Shum, Jonathan O’Neill, Sonya E. Aydin, Erkin Zhavoronkov, Alex Vidal, Anxo Soto, Atenea Alonso, Maria Jose Rosenberg, Ari J. Lingen, Mark W. D’Cruz, Anil Agrawal, Nishant Izumchenko, Evgeny |
author_sort | Goldberg, Manijeh |
collection | PubMed |
description | Despite therapeutic advancements, oral cavity squamous cell carcinoma (OCSCC) remains a difficult disease to treat. Systemic platinum-based chemotherapy often leads to dose-limiting toxicity (DLT), affecting quality of life. PRV111 is a nanotechnology-based system for local delivery of cisplatin loaded chitosan particles, that penetrate tumor tissue and lymphatic channels while avoiding systemic circulation and toxicity. Here we evaluate PRV111 using animal models of oral cancer, followed by a clinical trial in patients with OCSCC. In vivo, PRV111 results in elevated cisplatin retention in tumors and negligible systemic levels, compared to the intravenous, intraperitoneal or intratumoral delivery. Furthermore, PRV111 produces robust anti-tumor responses in subcutaneous and orthotopic cancer models and results in complete regression of carcinogen-induced premalignant lesions. In a phase 1/2, open-label, single-arm trial (NCT03502148), primary endpoints of efficacy (≥30% tumor volume reduction) and safety (incidence of DLTs) of neoadjuvant PRV111 were reached, with 69% tumor reduction in ~7 days and over 87% response rate. Secondary endpoints (cisplatin biodistribution, loco-regional control, and technical success) were achieved. No DLTs or drug-related serious adverse events were reported. No locoregional recurrences were evident in 6 months. Integration of PRV111 with current standard of care may improve health outcomes and survival of patients with OCSCC. |
format | Online Article Text |
id | pubmed-9385702 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93857022022-08-19 A nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer Goldberg, Manijeh Manzi, Aaron Birdi, Amritpreet Laporte, Brandon Conway, Peter Cantin, Stefanie Mishra, Vasudha Singh, Alka Pearson, Alexander T. Goldberg, Eric R. Goldberger, Sam Flaum, Benjamin Hasina, Rifat London, Nyall R. Gallia, Gary L. Bettegowda, Chetan Young, Simon Sandulache, Vlad Melville, James Shum, Jonathan O’Neill, Sonya E. Aydin, Erkin Zhavoronkov, Alex Vidal, Anxo Soto, Atenea Alonso, Maria Jose Rosenberg, Ari J. Lingen, Mark W. D’Cruz, Anil Agrawal, Nishant Izumchenko, Evgeny Nat Commun Article Despite therapeutic advancements, oral cavity squamous cell carcinoma (OCSCC) remains a difficult disease to treat. Systemic platinum-based chemotherapy often leads to dose-limiting toxicity (DLT), affecting quality of life. PRV111 is a nanotechnology-based system for local delivery of cisplatin loaded chitosan particles, that penetrate tumor tissue and lymphatic channels while avoiding systemic circulation and toxicity. Here we evaluate PRV111 using animal models of oral cancer, followed by a clinical trial in patients with OCSCC. In vivo, PRV111 results in elevated cisplatin retention in tumors and negligible systemic levels, compared to the intravenous, intraperitoneal or intratumoral delivery. Furthermore, PRV111 produces robust anti-tumor responses in subcutaneous and orthotopic cancer models and results in complete regression of carcinogen-induced premalignant lesions. In a phase 1/2, open-label, single-arm trial (NCT03502148), primary endpoints of efficacy (≥30% tumor volume reduction) and safety (incidence of DLTs) of neoadjuvant PRV111 were reached, with 69% tumor reduction in ~7 days and over 87% response rate. Secondary endpoints (cisplatin biodistribution, loco-regional control, and technical success) were achieved. No DLTs or drug-related serious adverse events were reported. No locoregional recurrences were evident in 6 months. Integration of PRV111 with current standard of care may improve health outcomes and survival of patients with OCSCC. Nature Publishing Group UK 2022-08-17 /pmc/articles/PMC9385702/ /pubmed/35977936 http://dx.doi.org/10.1038/s41467-022-31859-3 Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Goldberg, Manijeh Manzi, Aaron Birdi, Amritpreet Laporte, Brandon Conway, Peter Cantin, Stefanie Mishra, Vasudha Singh, Alka Pearson, Alexander T. Goldberg, Eric R. Goldberger, Sam Flaum, Benjamin Hasina, Rifat London, Nyall R. Gallia, Gary L. Bettegowda, Chetan Young, Simon Sandulache, Vlad Melville, James Shum, Jonathan O’Neill, Sonya E. Aydin, Erkin Zhavoronkov, Alex Vidal, Anxo Soto, Atenea Alonso, Maria Jose Rosenberg, Ari J. Lingen, Mark W. D’Cruz, Anil Agrawal, Nishant Izumchenko, Evgeny A nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer |
title | A nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer |
title_full | A nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer |
title_fullStr | A nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer |
title_full_unstemmed | A nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer |
title_short | A nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer |
title_sort | nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9385702/ https://www.ncbi.nlm.nih.gov/pubmed/35977936 http://dx.doi.org/10.1038/s41467-022-31859-3 |
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