Cancer Chemotherapy and Pharmacology· 2026Q2
CNS distribution and preclinical activity of the PI3K/AKT inhibitors inavolisib and ipatasertib in pediatric-type diffuse high-grade gliomas
- 0citations
- Q2SCImago
- 2026year
Short summary
The PI3K inhibitor inavolisib achieved therapeutic concentrations in the CNS and extended survival in preclinical models of pediatric-type diffuse high-grade gliomas (pHGG) with PIK3CA mutations, while the AKT inhibitor ipatasertib did not show significant in vivo efficacy.
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Key points
- Inavolisib and ipatasertib were tested against 12 pediatric-type diffuse high-grade glioma (pHGG) cell lines with PI3K/AKT alterations.
- Pharmacokinetic modeling in mice showed brain-to-plasma ratios of 0.07 for inavolisib and 0.20 for ipatasertib.
- Inavolisib significantly extended survival (P = 0.0070) and increased CSF ctDNA release (P = 0.0317) in intracranial PIK3CA-mutated pHGG xenografts.
- Ipatasertib did not demonstrate significant in vivo activity despite in vitro sensitivity.
AI-generated from the title and abstract; the full text is not read.
Abstract
Abstract Purpose Pediatric-type diffuse high-grade gliomas (pHGG) are aggressive, largely incurable malignancies often characterized by PI3K/AKT pathway activation. This study investigated whether the PI3K inhibitor inavolisib and the AKT inhibitor ipatasertib could achieve therapeutic concentrations in the central nervous system (CNS) and demonstrate efficacy against PIK3CA -mutated pHGG. Methods A panel of 12 pHGG cell lines with diverse PI3K/AKT genetic aberrations was screened for sensitivity to inavolisib and ipatasertib. Pharmacokinetic (PK) modeling was performed in mice to determine brain-to-plasma exposure ratios following oral administration (50 mg/kg inavolisib and 100 mg/kg ipatasertib). Finally, the in vivo efficacy of both inhibitors was evaluated using intracranial PIK3CA -mutated pHGG xenograft models, with survival and cerebrospinal fluid (CSF) circulating tumor DNA (ctDNA) levels as primary endpoints. Results All 12 cell lines exhibited PI3K/AKT alterations. The PIK3CA H1047R-mutated line (HSJD-DIPG-007) was the most sensitive in vitro (IC 50 = 0.016 µM for inavolisib; 0.52 µM for ipatasertib). PK modeling revealed geometric mean brain-to-plasma ratios of 0.07 for inavolisib and 0.20 for ipatasertib, with model-predicted maximum brain concentrations of 0.69 µM and 0.93 µM, respectively. In vivo, inavolisib significantly extended survival ( P = 0.0070) and increased CSF ctDNA release ( P = 0.0317). In contrast, ipatasertib did not demonstrate significant in vivo activity. Conclusion These findings highlight the therapeutic potential of inavolisib for treating PIK3CA -mutated pHGG. Despite the blood-brain barrier, inavolisib achieved sufficient CNS exposure to prolong survival in preclinical models, whereas ipatasertib efficacy did not translate from in vitro to in vivo settings.
The authors' abstract, as published at the source. Cancer Chemotherapy and Pharmacology, 2026 · DOI ↗
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Field: Genetics (Medicine)
GeneticsMedicine