Gliosarcoma: A Multi-Institutional Analysis on Clinical Outcomes and Prognostic Factors
- Siyer Roohani 1,2,3, Maximilian Mirwald 1, Felix Ehret 1,3, Christoph Fink 4,5,6, Laila König 4,5,6, Jana Käthe Striefler 7, Noelle Samira Jacob 7, Ilinca Popp 8,9, Johannes Steffel 8, Jolina Handtke 1, Noa Marie Claßen 1, Titus Rotermund 1, Daniel Zips 1,3, Peter Vajkoczy 10, Ulrich Schüller 11,12,13, Mateusz Jacek Spałek 14,15, David Kaul 1,3
- Siyer Roohani 1,2,3, Maximilian Mirwald 1, Felix Ehret 1,3
- 1Department of Radiation Oncology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
- 2BIH Charité Junior Clinician Scientist Program, Berlin Institute of Health at Charité-Universitätsmedizin Berlin, BIH Biomedical Innovation Academy, Berlin, Germany.
- 3German Cancer Consortium (DKTK), partner site Berlin, a partnership between DKFZ and Charité-Universitätsmedizin Berlin, Germany, Heidelberg, Germany.
- 4Department of Radiation Oncology, University Hospital Heidelberg, Heidelberg, Germany.
- 5National Center of Radiation Oncology, Heidelberg Institute of Radiation Oncology (HIRO), Heidelberg, Germany.
- 6National Center for Tumor Diseases (NCT), Heidelberg, Germany.
- 7Department of Internal Medicine II, Oncology/Hematology/BMT/Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
- 8Department of Radiation Oncology, Medical Center University of Freiburg, Faculty of Medicine, Freiburg, Germany.
- 9German Cancer Consortium (DKTK) Partner Site Freiburg, German Cancer Research Center (DKFZ), Im Neuenheimer Feld, Heidelberg, Germany.
- 10Department of Neurosurgery, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
- 11Department of Pediatric Hematology and Oncology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
- 12Research Institute Children's Cancer Center Hamburg, Hamburg, Germany.
- 13Institute of Neuropathology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
- 14Department of Soft Tissue/Bone Sarcoma and Melanoma, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
- 15Department of Radiotherapy I, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.
- 0Department of Radiation Oncology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin and Humboldt-Universität zu Berlin, Berlin, Germany.
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View abstract on PubMed
Summary
This summary is machine-generated.Trimodal therapy (surgery, radiotherapy, chemotherapy) improves survival for gliosarcoma (GSM) patients. Younger age, smaller tumors, and methylated MGMT promoters are favorable prognostic factors for GSM.
Area Of Science
- Neuro-oncology
- Surgical Oncology
- Radiation Oncology
- Medical Oncology
Background
- Gliosarcomas (GSM) are rare and aggressive primary brain tumors.
- Optimal treatment strategies and prognostic factors for GSM remain incompletely defined.
Purpose Of The Study
- To describe oncological outcomes in patients with gliosarcoma (GSM).
- To investigate prognostic factors influencing survival in GSM patients.
Main Methods
- Retrospective analysis of 170 histopathologically confirmed GSM patients from five European institutions.
- Evaluation of treatment modalities including surgery, postoperative radiotherapy (pRT), and temozolomide (TMZ)-based chemotherapy.
- Multivariable Cox regression analysis (MVA) to identify significant prognostic factors for overall survival (OS) and progression-free survival (PFS).
Main Results
- The median OS and PFS were 12.3 and 6.6 months, respectively.
- Trimodal therapy (surgery, pRT, TMZ chemotherapy) was associated with improved survival.
- Significant prognostic factors for OS included younger age, gross total resection (GTR), pRT, TMZ chemotherapy, methylated MGMT promoter, and smaller tumor diameter.
- Significant prognostic factors for PFS included GTR, pRT, TMZ chemotherapy, unknown MGMT promoter status, and smaller tumor diameter.
Conclusions
- Trimodal therapy appears to be the most beneficial treatment approach for GSM.
- Factors associated with improved survival include younger age, smaller tumor size, and methylated MGMT promoters.
- This study represents the largest multi-institutional cohort investigating outcomes and prognostic factors for GSM.
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