TY - JOUR
T1 - A nanoengineered topical transmucosal cisplatin delivery system induces anti-tumor response in animal models and patients with oral cancer
AU - Goldberg, Manijeh
AU - Manzi, Aaron
AU - Conway, Peter
AU - Cantin, Stefanie
AU - Mishra, Vasudha
AU - Singh, Alka
AU - Pearson, Alexander T.
AU - Goldberg, Eric R.
AU - Goldberger, Sam
AU - Flaum, Benjamin
AU - Hasina, Rifat
AU - London, Nyall R.
AU - Gallia, Gary L.
AU - Bettegowda, Chetan
AU - O’Neill, Sonya E.
AU - Aydin, Erkin
AU - Zhavoronkov, Alex
AU - Vidal, Anxo
AU - Soto, Atenea
AU - Alonso, Maria Jose
AU - Rosenberg, Ari J.
AU - Lingen, Mark W.
AU - D’Cruz, Anil
AU - Agrawal, Nishant
AU - Izumchenko, Evgeny
N1 - Funding Information:
This 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.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - 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.
AB - 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.
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U2 - 10.1038/s41467-022-31859-3
DO - 10.1038/s41467-022-31859-3
M3 - Article
C2 - 35977936
AN - SCOPUS:85136022839
SN - 2041-1723
VL - 13
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 4829
ER -