# Development of an integrated risk stratification model for metastatic medulloblastoma (M2/3) using clinical, radiologic, and molecular variables

**Authors:** Wen-Tao Zhou, Tao Wu, Yu-Fei Lu, Shu-Xu Du, Han-Guang Zhao, Si-Kang Ren, Chi Zhao, Yong-Ji Tian, Fu Zhao

PMC · DOI: 10.1093/noajnl/vdaf265 · 2025-12-22

## TL;DR

This study develops a new risk model for metastatic medulloblastoma using clinical, radiologic, and molecular data to improve treatment strategies for high-risk patients.

## Contribution

A novel integrated risk stratification model combining clinical, radiologic, and molecular variables for metastatic medulloblastoma.

## Key findings

- The 5-year event-free survival and overall survival rates were 56.1% and 68.7%, respectively.
- Molecular subgrouping, metastatic patterns, and the 'sandwich' strategy were independent prognostic predictors.
- The 'sandwich' strategy significantly improved survival outcomes in patients with metastatic medulloblastoma.

## Abstract

Approximately 20% of medulloblastoma (MB) patients are diagnosed with metastatic disease and typically exhibit extremely poor clinical outcomes. This study aimed to investigate potential prognostic factors affecting the survival of patients with metastatic MB.

Patients with initial diagnosis of metastatic MB (M2/3) at Beijing Tiantan Hospital were included. Radiological characteristics were discerned through a retrospective review. Overall survival (OS) and event-free survival (EFS) were calculated using the Kaplan-Meier analysis. Multivariable Cox proportional hazards model was employed to identify potential prognostic factors.

This study included 115 patients with M2/3 MB. Group 4 MBs accounted for 59.1% of cases (68/115). Kaplan-Meier analysis indicated that the 5-year EFS and OS rates were 56.1% and 68.7%, respectively. Patients with metastatic Group 3 MB and spinal metastases exhibited dismal outcomes. Postoperative “sandwich” strategy significantly prolonged 5-year EFS and OS rates. Multivariate COX regression models demonstrated that molecular subgrouping, metastatic patterns, and “sandwich” strategy were independent prognostic predictors for both EFS and OS in patients with M2/3 MB.

Our study provides a novel risk stratification model for metastatic medulloblastoma that could potentially facilitate the development of individualized therapeutic strategies for the very high-risk patient population.

## Linked entities

- **Diseases:** medulloblastoma (MONDO:0002794)

## Full-text entities

- **Genes:** SHH (sonic hedgehog signaling molecule) [NCBI Gene 6469] {aka HHG1, HLP3, HPE3, MCOPCB5, SMMCI, ShhNC}, TP53 (tumor protein p53) [NCBI Gene 7157] {aka BCC7, BMFS5, LFS1, P53, TRP53}, MYCN (MYCN proto-oncogene, bHLH transcription factor) [NCBI Gene 4613] {aka FGLDS1, MODED, MPAPA, MYCNsORF, MYCNsPEP, N-myc}, MYC (MYC proto-oncogene, bHLH transcription factor) [NCBI Gene 4609] {aka MRTL, MYCC, bHLHe39, c-Myc}
- **Diseases:** brain tumor (MESH:D001932), ototoxicity (MESH:D006311), Toxicity (MESH:D064420), HIT (MESH:D013921), desmoplastic (MESH:D018220), infection (MESH:D007239), neurocognitive sequelae (MESH:D019965), death (MESH:D003643), neutropenia (MESH:D009503), Metastases (MESH:D009362), nodular disease (MESH:D008224), CMBs (MESH:D008527), MBs (MESH:C567291), M1 disease (MESH:D016537), intracranial hemorrhage (MESH:D020300), Metastatic (MESH:D000092182), Tumor (MESH:D009369), neurotoxicity (MESH:D020258)
- **Chemicals:** formalin (MESH:D005557), eosin (MESH:D004801), lomustine (MESH:D008130), etoposide (MESH:D005047), carboplatin (MESH:D016190), Hematoxylin (MESH:D006416), SJMB03 (-), cisplatin (MESH:D002945), cyclophosphamide (MESH:D003520), methotrexate (MESH:D008727), vincristine (MESH:D014750), paraffin (MESH:D010232)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12924635/full.md

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Source: https://tomesphere.com/paper/PMC12924635