Journal of clinical oncology : official journal of the American Society of Clinical Oncology
October 14, 2026 · via Europe PMC
Neurodevelopmental Blueprint in Gliomas: Toward an Ontogenetic Multimodal Integrated Therapy.
Padevit L, Weiss T, Vasella F, +6 more, Akeret K
AI summary — for doctors, generated from the abstract only
This review proposes that gliomas re-enact brain development in reverse, suggesting treatment tailored to tumor anatomy and developmental stage.
What was studied
Narrative review integrating molecular, single-cell, histoarchitectural and anatomic evidence on diffuse gliomas and embryonal tumors, proposing an ontogenetic multimodal integrated therapy concept.
Key findings
- Proposes tumor transformation and dedifferentiation mirror and invert normal brain ontogeny
- Framework aims to explain mosaicism, directional spread and resistant tumor-propagating cell states
- Suggests aligning surgery, radiotherapy and drug therapy with tumor stage and compartments rather than visible bulk
Clinical relevance
Neuro-oncologists and neurosurgeons may find a conceptual lens for planning treatment and monitoring.
Who should care
Limitations
A conceptual synthesis presenting hypotheses without new clinical data or outcome testing.
Thought-provoking, but needs prospective validation before it could guide care.
This is an AI-generated summary of the published abstract, not a clinical recommendation. It may not reflect the full text or subsequent updates — verify against the original source before acting on it.
Abstract
Neuroepithelial tumors, including diffuse gliomas and embryonal neoplasms, remain among the most lethal cancers despite major advances in molecular diagnostics and some novel targeted therapies for subsets of patients. A persistent barrier to progress is the lack of a unifying framework that integrates their cellular hierarchy, spatial heterogeneity, and distinctive patterns of progression. In this review, we synthesize converging evidence that neuroepithelial tumor biology represents a pathologic re-enactment of brain ontogeny. Integrating molecular, single-cell, histoarchitectonic, and anatomic observations, we propose that neoplastic transformation, aberrant lineage commitment, and dedifferentiation mirror and invert physiological ontogenetic trajectories. This ontogenetic logic provides a coherent explanation for key hallmarks of neuroepithelial tumors, including intratumoral mosaicism, directional anatomic spread, and the emergence of therapy-resistant tumor-propagating cell states. Ontogenetic multimodal integrated therapy is an anatomy-guided strategy that aligns neurosurgery, radiotherapy, and pharmacotherapy with tumor stage and ontogenetic architecture. By shifting emphasis from radiologically visible tumor bulk to compartment-based developmental logic, this framework offers testable hypotheses and a clinically oriented paradigm for diagnosis, treatment planning, and longitudinal monitoring in patients with neuroepithelial tumors.
DOI
10.1200/JCO-25-02798
PMID
42874018
Research metadata (titles, abstracts, authors, publication dates) is sourced from Europe PMC, which aggregates content from PubMed/MEDLINE, PubMed Central, and other providers under the U.S. National Library of Medicine (NLM/NCBI). NLM does not claim copyright on abstracts; the original journal publishers or authors may hold rights to the full articles. AI-generated summaries are derived only from the abstract, never the full text, and are always labeled as AI-generated.
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