ONC206 demonstrates potent anti-tumorigenic activity and is a potential novel therapeutic strategy for high-risk medulloblastoma

Tzaridis, T. D.; Liu, J.; Chien, F. L.; Malhotra, A.; Zhu, D.; Gershon, I.; Zhang, H.; Velazquez Vega, J. E.; Schniederjan, M.; Sposito, T.; Adams, P. D.; Allen, J. E.; Prabhu, V. V.; Wechsler-Reya, R.; MacDonald, T. J.

doi:10.1101/2025.09.25.678693

bioRxiv · 10.1101/2025.09.25.678693

ONC206 demonstrates potent anti-tumorigenic activity and is a potential novel therapeutic strategy for high-risk medulloblastoma

Tzaridis, T. D.·Liu, J.·Chien, F. L.·Malhotra, A.·Zhu, D.·Gershon, I.·Zhang, H.·Velazquez Vega, J. E.·Schniederjan, M.·Sposito, T.·Adams, P. D.·Allen, J. E.·Prabhu, V. V.·Wechsler-Reya, R.·MacDonald, T. J.

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Abstract

BackgroundMedulloblastoma is the most common malignant pediatric brain tumor, and has an urgent need for novel treatment approaches. Dordaviprone (ONC201) and its chemical derivative with nanomolar potency, ONC206, induce apoptosis of cancer cells by activation of the mitochondrial caseinolytic protease P (ClpP). ONC206 is currently in Phase I clinical trials for pediatric patients with primary brain tumors. MethodsIn this study, we evaluated the preclinical therapeutic effects of ONC206 in medulloblastoma and investigated its mechanism of action. ResultsWe found evidence for high expression of ClpP at both the RNA and protein level in medulloblastoma tumors, compared to very low expression in normal brain tissue. In addition, we saw a pronounced reduction in cell viability of human Group 3 and Group 4 and murine SHH-driven and Group 3 medulloblastoma cells treated with ONC206 with low IC-50s. After treatment with ONC206, we observed an induction of integrated stress response and mitochondrial damage. To test the efficacy of ONC206 in vivo, we used murine models of SHH-driven and Group 3 medulloblastoma as well as Group 3 and Group 4 patient-derived xenografts (PDXs). ONC206 led to a significant prolongation of survival in both murine models, with the SHH mice demonstrating survival extension from 70 to 140 days. PDX-bearing mice also responded to ONC206, which led to a significant survival benefit. ConclusionOur results highlight ONC206 as a novel therapeutic option for patients with high-risk medulloblastoma and provide strong rationale for testing the efficacy of ONC206 in the treatment of these patients. Key points (2-3)ONC206 potently kills medulloblastoma cells by inducing integrated stress response and mitochondrial damage. ONC206 prolongs survival of medulloblastoma-bearing mice in both murine and patient-derived xenograft models. Importance of studyThere is an unmet need for better therapies for high-risk medulloblastoma patients. ONC201 has shown promising responses and recently received FDA approval for diffuse midline glioma. ONC206 is a chemical derivative with higher potency and better brain penetrance. In this study, we analyzed the therapeutic potential of ONC206 for high-risk medulloblastoma and found that the drug effectively killed mouse and human medulloblastoma cells with high nanomolar potency. We also saw that ONC206 very significantly prolonged survival of medulloblastoma-bearing mice, both in genetically engineered mouse models and patient-derived xenografts. Our study provides a strong rationale for testing the efficacy of ONC206 in the treatment of patients with medulloblastoma and has set the stage for a clinical trial with this agent in pediatric patients with recurrent malignant brain tumors, including medulloblastoma (NCT04732065).

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Tzaridis, T. D., Liu, J., Chien, F. L., Malhotra, A., Zhu, D., Gershon, I., Zhang, H., Velazquez Vega, J. E., Schniederjan, M., Sposito, T., Adams, P. D., Allen, J. E., Prabhu, V. V., Wechsler-Reya, R., MacDonald, T. J.. 2025-09-29. ONC206 demonstrates potent anti-tumorigenic activity and is a potential novel therapeutic strategy for high-risk medulloblastoma. https://doi.org/10.1101/2025.09.25.678693

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