The War Against Glioblastoma Needs More Than Standard of Care
Stefaan W Van Gool, Jennifer Kosmal, Linde Kampers
Improving overall survival for patients with Glioblastoma remains a challenge. We installed individualized multimodal immunotherapy as part of a multiphase combined treatment strategy (PMID 38548421). For the current real world data analysis, 104 patients were selected out of the database with the criteria: treatment after 27/05/2015, adults between 18 and 70y, GB diagnosis documented IDH1wt status, known status of OS, absence of second malignancy and known MGMT promoter methylation status (meth versus unmeth).
Sex distribution was 18 female / 25 male in meth patients versus 23 /38 in unmeth patients. Median age at intake was 54y versus 50y. The extent of resection was 12 R0, 28 < R0 and 3 not available versus 25, 28 and 8. Median KPI at intake was 70 and 70. Patients received in median 37 versus 31 sessions of mEHT, 37 versus 32 injections of NDV and 2 versus 1 DC vaccines. Median OS and percentage 2y OS were 30 months and 69.8% in meth patients versus 20 months and 37.4% in unmeth patients.
There were no major adverse reactions (AR), but the burden of AR is increasing when using checkpoint inhibitors. The beneficial effect of this treatment strategy on OS and quality of life in a larger group of real world patients confirms earlier data. It remains unclear how to draw evidence out of individualized medicine, although it is felt necessarily for patients with Glioblastoma.
Stefaan W Van Gool, Jennifer Kosmal, Linde Kampers
Improving overall survival for patients with Glioblastoma remains a challenge. We installed individualized multimodal immunotherapy as part of a multiphase combined treatment strategy (PMID 38548421). For the current real world data analysis, 104 patients were selected out of the database with the criteria: treatment after 27/05/2015, adults between 18 and 70y, GB diagnosis documented IDH1wt status, known status of OS, absence of second malignancy and known MGMT promoter methylation status (meth versus unmeth).
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Sex distribution was 18 female / 25 male in meth patients versus 23 /38 in unmeth patients. Median age at intake was 54y versus 50y. The extent of resection was 12 R0, 28 < R0 and 3 not available versus 25, 28 and 8. Median KPI at intake was 70 and 70. Patients received in median 37 versus 31 sessions of mEHT, 37 versus 32 injections of NDV and 2 versus 1 DC vaccines. Median OS and percentage 2y OS were 30 months and 69.8% in meth patients versus 20 months and 37.4% in unmeth patients.
There were no major adverse reactions (AR), but the burden of AR is increasing when using checkpoint inhibitors. The beneficial effect of this treatment strategy on OS and quality of life in a larger group of real world patients confirms earlier data. It remains unclear how to draw evidence out of individualized medicine, although it is felt necessarily for patients with Glioblastoma.
Stefaan Van Gool
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Read the Abstracts from Our Invited Speakers
Cancer Biology
- AllergoOncology: Lessons Learned from the Allergy-Glioblastoma Connection
Aurélie Poli, Luxembourg Institute of Health, LUXEMBOURG
- Cytotoxic NK Cells Impede Response to Checkpoint Immunotherapy in Melanoma with an Immune-Excluded Phenotype
Joanna Poźniak, KU Leuven, BELGIUM
- Inducing Immunogenic Tertiary Lymphoid Structures Across Cancer Types With Dendritic Cell Reprogramming
Camille Chatelain, Lund University, SWEDEN
- The Role of ILC2 in Tissue Homeostasis and Neoplasia
Tim Halim, Cancer Research UK Cambridge Institute, UNITED KINGDOM
Cancer Neuroscience
- Latent Neuropathy in Colorectal Cancer: Implications for Cancer Survivorship
Andrew Shepherd, University of Texas MD Anderson Cancer Center, USA
- Remodelling of the Bone Microenvironment During Cancer Infiltration: Insights from Multiplex Imaging and Spatial Transcriptomics
Christina Møller Andreasen, University of Southern Denmark, DENMARK
- Enteric Nervous System-Derived VIP Restrains Differentiation of LGR5+ Stem Cells Towards the Secretory Lineage Impeding Type 2 Immune Programs
Christoph Klose, Charité – Berlin University Medicine, GERMANY
Cancer Therapy
- Targeting the Dark Matter of Cancer with AI-Designed Mini Binder
Tobias Bald, University of Bonn, DEUTSCHLAND
- Engineering Nanomedicines for Targeted Neuroimmune Modulation
Helena Florindo, University of Lisbon, PORTUGAL
- Potentiating Immunotherapy of Urological Cancers with Oncolytic Viruses
Gabriel van der Pluijm
- Cancer Neuroscience of Brain Tumors: From Basic Discoveries to Clinical TrialsKEYNOTE SPEAKER
Frank Winkler, Universitätsklinik Heidelberg, DEUTSCHLAND
- TBC
Sheeba Irshad, King’s College London, UNITED KINGDOM
- The War Against Glioblastoma Needs More Than Standard of Care
Stefaan Van Gool, IOZK Immun-Onkologisches Zentrum Köln, DEUTSCHLAND
- Uncovering the Spatial Regulation of γδ T Cells: Toward Receptor-Guided Immunotherapy
Jürgen Kuball, University Medical Center Utrecht, NETHERLANDS
- TBC
Jarosław Dybko, Lower Silesian Oncology Center in Wroclaw, POLAND
- Expanding CAR Targets to Non Protein Antigens
Sébastien Wälchli, Oslo University Hospital, NORWAY
- TBC
Helen Kakkassery, King’s College London, UNITED KINGDOM