Atypical Teratoid/Rhabdoid Tumor of the Lateral Ventricle: A Case Series and Experience with Molecular Subtyping-Guided Immunotherapy

BACKGROUND: tumor-infiltrating lymphocytes, indicating immunogenic potential. CASE PRESENTATION: We report three pediatric cases presenting with intracranial hypertension and seizures. Diagnosis was confirmed via histopathology and molecular profiling. Interventions included gross total resection, chemotherapy, radiotherapy, and combined immune checkpoint inhibitors (pembrolizumab and ipilimumab). Outcomes varied from rapid progression to 3-year recurrence-free survival. A cohort of 14 pediatric patients with lateral ventricle AT/RT, comprising 3 institutional cases and 11 cases identified from the PubMed database, was evaluated through a narrative synthesis. CONCLUSIONS: These advancements highlight the crucial role of molecular subtyping in tailoring personalized treatments, including epigenetic modifiers and immune-based regimens. However, clinical validation is essential to establish standardized protocols. Integrating genomic, epigenetic, and immune microenvironment profiling may enhance risk assessment and treatment precision, ultimately improving survival and quality of life in pediatric patients.

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Publication Details

Journal
Neurology International
Published
2026-04-21
DOI
https://doi.org/10.3390/neurolint18040074
Primary Topic
Chromatin Remodeling and Cancer
Type
article
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article

Atypical Teratoid/Rhabdoid Tumor of the Lateral Ventricle: A Case Series and Experience with Molecular Subtyping-Guided Immunotherapy

Nijia Zhang, Yingjie Cai, Yi-Xiang Wang, Zhuo Zhi et al.
Neurology International
Chromatin Remodeling and Cancer
article

Atypical Teratoid/Rhabdoid Tumor of the Lateral Ventricle: A Case Series and Experience with Molecular Subtyping-Guided Immunotherapy

Nijia Zhang, Yingjie Cai, Yi-Xiang Wang, Zhuo Zhi, Zesheng Ying, Nan Zhang, Haohan Wang
article en

Abstract

BACKGROUND: tumor-infiltrating lymphocytes, indicating immunogenic potential. CASE PRESENTATION: We report three pediatric cases presenting with intracranial hypertension and seizures. Diagnosis was confirmed via histopathology and molecular profiling. Interventions included gross total resection, chemotherapy, radiotherapy, and combined immune checkpoint inhibitors (pembrolizumab and ipilimumab). Outcomes varied from rapid progression to 3-year recurrence-free survival. A cohort of 14 pediatric patients with lateral ventricle AT/RT, comprising 3 institutional cases and 11 cases identified from the PubMed database, was evaluated through a narrative synthesis. CONCLUSIONS: These advancements highlight the crucial role of molecular subtyping in tailoring personalized treatments, including epigenetic modifiers and immune-based regimens. However, clinical validation is essential to establish standardized protocols. Integrating genomic, epigenetic, and immune microenvironment profiling may enhance risk assessment and treatment precision, ultimately improving survival and quality of life in pediatric patients.

Neurology InternationalVol. 18(4)
Capital Medical University (CN), Beijing Children’s Hospital (CN)
Openalex Percentile: Top 16%
Chromatin Remodeling and Cancer
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