Toxicity and Biodistribution of the Oncolytic Virus VCN-01 Following Intracranial Injection in Syrian Hamsters

Among solid pediatric tumors, brain tumors are the leading cause of cancer-related mortality. While survival rates have improved for certain pediatric brain tumor subtypes, the overall prognosis remains poor. Consequently, there is an urgent need for novel therapies that are not only effective but also less toxic. Oncolytic viruses have emerged as promising therapeutic agents due to their ability to selectively replicate in tumor cells while sparing healthy tissue and their potential to induce systemic antitumor immune responses. VCN-01 is a replication-competent oncolytic adenovirus whose efficacy has been demonstrated in clinical trials after systemic administration in combination with chemotherapy. Evidence of antitumor activity has also been obtained after intracranial administration in preclinical models of various brain tumors, including high-grade gliomas. However, before progressing to clinical trials for those indications, it is essential to assess the safety of its intracranial administration. In this study, we evaluated the toxicity and biodistribution of VCN-01 following intracranial injection in a Syrian hamster model. Two viral doses were tested: 1.5 × 10<sup>9</sup> and 1.5 × 10<sup>10</sup> viral particles (vp)/animal, corresponding to 5 and 50 times the starting clinical dose (10<sup>10</sup> vp/patient), respectively. Our toxicity analysis revealed a favorable safety profile, with no adverse effects observed following administration. Biodistribution studies demonstrated that VCN-01 primarily remained confined to the brain, with only minimal presence detected in peripheral tissues. The neutralizing antibody response against the virus was stronger in females than in males, correlating with a lower detection of vp in females compared with males. In conclusion, these findings support the safety of intracranial administration of VCN-01 and provide a strong rationale for its further development as a therapeutic option for patients with brain tumors.

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Journal
Human Gene Therapy
Published
2025-08-29
DOI
https://doi.org/10.1177/10430342251372091
Primary Topic
Virus-based gene therapy research
Type
article
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article

Toxicity and Biodistribution of the Oncolytic Virus VCN-01 Following Intracranial Injection in Syrian Hamsters

Ana Patiño‐García, Marta M. Alonso, Jaime Gállego Pérez‐Larraya, Lilian Zavala‐Romero et al.
Human Gene Therapy
Virus-based gene therapy research
article

Toxicity and Biodistribution of the Oncolytic Virus VCN-01 Following Intracranial Injection in Syrian Hamsters

Ana Patiño‐García, Marta M. Alonso, Jaime Gállego Pérez‐Larraya, Lilian Zavala‐Romero, Miriam Bazán‐Peregrino, Lucía Marrodán, Manel Cascalló, Ana Mato-Berciano, Marisol González-Huarriz, Iker Ausejo-Mauleón, Ramón Alemany, Marta Zalacaín, Daniel Palacios-Alonso
article en

Abstract

Among solid pediatric tumors, brain tumors are the leading cause of cancer-related mortality. While survival rates have improved for certain pediatric brain tumor subtypes, the overall prognosis remains poor. Consequently, there is an urgent need for novel therapies that are not only effective but also less toxic. Oncolytic viruses have emerged as promising therapeutic agents due to their ability to selectively replicate in tumor cells while sparing healthy tissue and their potential to induce systemic antitumor immune responses. VCN-01 is a replication-competent oncolytic adenovirus whose efficacy has been demonstrated in clinical trials after systemic administration in combination with chemotherapy. Evidence of antitumor activity has also been obtained after intracranial administration in preclinical models of various brain tumors, including high-grade gliomas. However, before progressing to clinical trials for those indications, it is essential to assess the safety of its intracranial administration. In this study, we evaluated the toxicity and biodistribution of VCN-01 following intracranial injection in a Syrian hamster model. Two viral doses were tested: 1.5 × 10<sup>9</sup> and 1.5 × 10<sup>10</sup> viral particles (vp)/animal, corresponding to 5 and 50 times the starting clinical dose (10<sup>10</sup> vp/patient), respectively. Our toxicity analysis revealed a favorable safety profile, with no adverse effects observed following administration. Biodistribution studies demonstrated that VCN-01 primarily remained confined to the brain, with only minimal presence detected in peripheral tissues. The neutralizing antibody response against the virus was stronger in females than in males, correlating with a lower detection of vp in females compared with males. In conclusion, these findings support the safety of intracranial administration of VCN-01 and provide a strong rationale for its further development as a therapeutic option for patients with brain tumors.

Human Gene TherapyVol. 36(17-18)
Bellvitge University Hospital (ES), Institut d'Investigació Biomédica de Bellvitge (ES), Institut Català d'Oncologia (ES), Institut de Seguretat Pública de Catalunya (ES), Navarre Institute of Health Research (ES), Clinica Universidad de Navarra (ES), Universidad de Navarra (ES)
Openalex Percentile: Top 75%
Virus-based gene therapy research
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