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dc.contributor.authorGoldberg, M.
dc.contributor.authorManzi, A.
dc.contributor.authorConway, P.
dc.contributor.authorCantin, S.
dc.contributor.authorMishra, V.
dc.contributor.authorSingh, A.
dc.contributor.authorPearson, A.T.
dc.contributor.authorGoldberg, E.R.
dc.contributor.authorGoldberger, S.
dc.contributor.authorFlaum, B.
dc.contributor.authorHasina, R.
dc.contributor.authorLondon, N.R.
dc.contributor.authorGallia, G.L.
dc.contributor.authorBettegowda, C.
dc.contributor.authorO'Neill, S.E.
dc.contributor.authorAydin, E.
dc.contributor.authorZhavoronkov, A.
dc.contributor.authorVidal Figueroa, Anxo
dc.contributor.authorSoto, A.
dc.contributor.authorAlonso Fernández, María José
dc.contributor.authorRosenberg, A.J.
dc.contributor.authorLingen, M.W.
dc.contributor.authorD'Cruz, A.
dc.contributor.authorAgrawal, N.
dc.contributor.authorIzumchenko, E.
dc.date.accessioned2025-08-26T09:34:22Z
dc.date.available2025-08-26T09:34:22Z
dc.date.issued2022
dc.identifier.citationGoldberg M, Manzi A, Conway P, Cantin S, Mishra V, Singh A, et al. A nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer. Nature Communications. 2022;13(1).
dc.identifier.issn2041-1723
dc.identifier.otherhttps://portalcientifico.sergas.gal/documentos/631ce8ff63e72b10525637e5*
dc.identifier.urihttp://hdl.handle.net/20.500.11940/20693
dc.description.abstractDespite 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.en
dc.description.sponsorshipThis work was supported by the NIH grants R43 DE023725 and R44 CA192875, FDA Office of Orphan Products Development grant R01 FD006325, and National Science Foundation Award NSF IIP-1315084. E.I. effort was supported by the NIH grant R01DE027809. E.A. salary for partially supported by the TUBITAK 2219 postdoctoral research scholarship.en
dc.language.isoeng
dc.rightsAtribución 4.0 Internacional*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.titleA nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer*
dc.typeArticleen
dc.authorsophosGoldberg, E. M.
dc.authorsophosManzi, A.
dc.authorsophosConway, P.
dc.authorsophosCantin, S.
dc.authorsophosMishra, V.
dc.authorsophosSingh, A.
dc.authorsophosPearson, A. T.
dc.authorsophosGoldberg, E. R.
dc.authorsophosGoldberger, S.
dc.authorsophosFlaum, B.
dc.authorsophosHasina, R.
dc.authorsophosLondon, N. R.
dc.authorsophosGallia, G. L.
dc.authorsophosBettegowda, C.
dc.authorsophosO'Neill, S. E.
dc.authorsophosAydin, E.
dc.authorsophosZhavoronkov, A.
dc.authorsophosVidal, A.
dc.authorsophosSoto, A.
dc.authorsophosAlonso, M. J.
dc.authorsophosRosenberg, A. J.
dc.authorsophosLingen, M. W.
dc.authorsophosD'Cruz, A.
dc.authorsophosAgrawal, N.
dc.authorsophosIzumchenko
dc.identifier.doi10.1038/s41467-022-31859-3
dc.identifier.sophos631ce8ff63e72b10525637e5
dc.issue.number1
dc.journal.titleNature Communications*
dc.relation.projectIDNIH [R01DE027809, R43 DE023725, R44 CA192875]; FDA Office of Orphan Products Development grant [R01 FD006325]; National Science Foundation Award [NSF IIP-1315084]; TUBITAK [2219]; Food and Drug Administration [R01FD006325] Funding Source: NIH RePORTER
dc.relation.publisherversionhttps://www.nature.com/articles/s41467-022-31859-3.pdfes
dc.rights.accessRightsopenAccess
dc.subject.keywordAS Santiagoes
dc.subject.keywordIDISes
dc.typefidesArtículo Científico (incluye Original, Original breve, Revisión Sistemática y Meta-análisis)es
dc.typesophosArtículo Originales
dc.volume.number13


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