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Translational Medicine / 转化医学Glioblastoma & High-Grade Glioma

Michael Weller

MD

🏢University Hospital Zurich🌐Switzerland

Chair, Department of Neurology; Professor of Neurology, University of Zurich

90
h-index
4
Key Papers
4
Awards
4
Key Contributions

👥Biography 个人简介

Michael Weller, MD is Chair of the Department of Neurology at University Hospital Zurich and Professor of Neurology at the University of Zurich. He is a leading European neuro-oncologist recognized internationally for his work on molecular biomarkers in glioma—especially MGMT promoter methylation—and for leading pivotal clinical trials in high-grade glioma. His laboratory and clinical research programs have been instrumental in delineating the molecular taxonomy of gliomas and translating biomarker discoveries into clinical practice. Dr. Weller has led or co-led numerous landmark EORTC trials in glioma, including the phase III NOA-08 and CeTeG/NOA-09 trials. The CeTeG/NOA-09 trial demonstrated that CCNU plus temozolomide conferred a significant overall survival benefit compared to temozolomide alone in patients with newly diagnosed, MGMT-methylated GBM, leading to widespread adoption of this regimen for this molecular subgroup. He has served as chair of the EORTC Brain Tumor Group and plays a central role in shaping European clinical trial infrastructure and guideline development through EANO. His translational research encompasses glioma immunology, the tumor microenvironment, and resistance mechanisms to both chemotherapy and immunotherapy. Dr. Weller has authored or co-authored over 500 peer-reviewed publications and is among the most highly cited investigators in neuro-oncology. He serves on the editorial boards of major neuro-oncology journals and has mentored a wide network of European neuro-oncology investigators.

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🧪Research Fields 研究领域

MGMT Methylation
CCNU/Temozolomide Combinations
Glioma Molecular Pathology
Immunotherapy in Glioma
EORTC Brain Tumor Group

🎓Key Contributions 主要贡献

MGMT Methylation as Biomarker and Therapeutic Target

Made fundamental contributions to establishing MGMT promoter methylation as the most clinically actionable predictive biomarker in GBM, including validation across multiple independent phase III datasets and guidance for its integration into clinical decision-making for elderly and newly diagnosed GBM patients.

CCNU/Temozolomide (CeTeG/NOA-09 Trial)

Led the CeTeG/NOA-09 phase III trial demonstrating that CCNU plus TMZ improved median OS to 48.1 months vs. 31.4 months with TMZ alone in MGMT-methylated newly diagnosed GBM, establishing a new standard-of-care option for this biomarker-defined subgroup.

Glioma Molecular Classification and EANO Guidelines

Central contributor to the EANO clinical guidelines for the diagnosis and treatment of diffuse gliomas in adults, incorporating the WHO 2016 and 2021 molecular classification updates into evidence-based clinical recommendations.

Immunotherapy Resistance in GBM

Conducted key translational studies of checkpoint blockade and vaccine-based immunotherapy in GBM, including analyses of the CheckMate 143 trial, delineating why GBM resists PD-1 blockade and identifying potential predictive biomarkers for immune response.

Representative Works 代表性著作

[1]

CCNU-temozolomide combination therapy for newly diagnosed glioblastoma with MGMT promoter methylation (CeTeG/NOA-09)

Lancet (2019)

Phase III trial demonstrating superior OS with CCNU+TMZ vs. TMZ alone in MGMT-methylated newly diagnosed GBM (48.1 vs. 31.4 months), establishing a new treatment paradigm.

[2]

Temozolomide versus standard 6-week radiotherapy versus hypofractionated radiotherapy in patients older than 60 years with glioblastoma (NOA-08)

Lancet Oncology (2012)

Phase III trial demonstrating non-inferiority of TMZ alone vs. RT in elderly GBM patients, and that MGMT methylation predicts TMZ benefit, supporting biomarker-adapted treatment.

[3]

European Association for Neuro-Oncology (EANO) guideline on the diagnosis and treatment of adult astrocytic and oligodendroglial gliomas

Lancet Oncology (2017)

Comprehensive EANO clinical guidelines incorporating molecular classification (IDH, MGMT, 1p/19q) into treatment algorithms for diffuse gliomas.

[4]

Nivolumab versus bevacizumab in patients with recurrent glioblastoma (CheckMate 143)

Lancet Oncology (2017)

Phase III trial finding no OS benefit with nivolumab vs. bevacizumab in unselected recurrent GBM, with Dr. Weller contributing key biomarker analyses.

🏆Awards & Recognition 奖项与荣誉

🏆EANO Honorary Membership
🏆Swiss Cancer Research Foundation Award
🏆EORTC Brain Tumor Group Chair
🏆European Academy of Neurology Fellow

📄Data Sources 数据来源

Last updated: 2026-04-05 | All information from publicly available academic sources

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