Towards Image - Based Personalization of Glioblastoma Therapy: A Clinical and Biological Validation Study of a Novel, Deep Learning - Driven Tumor Growth Model

Author:

Metz Marie-Christin1ORCID,Ezhov Ivan23,Peeken Jan C456,Buchner Josef A4,Lipkova Jana7,Kofler Florian1283,Waldmannstetter Diana2,Delbridge Claire4,Diehl Christian9,Bernhardt Denise456,Schmidt-Graf Friederike10,Gempt Jens1112ORCID,Combs Stephanie E456,Zimmer Claus1,Menze Bjoern213,Wiestler Benedikt1ORCID

Affiliation:

1. Department of Diagnostic and Interventional Neuroradiology, Technical University of Munich , Munich, Germany

2. Department of Informatics, Technical University of Munich , Munich, Germany

3. TranslaTUM – Central Institute for Translational Cancer Research, Technical University of Munich , Munich, Germany

4. Department of Radiation Oncology, Technical University of Munich , Munich, Germany

5. Institute of Radiation Medicine (IRM), Department of Radiation Sciences (DRS), Helmholtz Zentrum München , Munich, Germany

6. Deutsches Konsortium für Translationale Krebsforschung (DKTK), Partner Site Munich , Munich, Germany

7. Department of Pathology, Brigham and Women's Hospital, Harvard Medical School , Boston, MA, USA

8. Helmholtz AI, Helmholtz Zentrum Munich , Munich, Germany

9. Department of Neuropathology, Institute of Pathology, Technical University of Munich , Munich, Germany

10. Department of Neurology, Technical University of Munich , Munich, Germany

11. Department of Neurosurgery, Technical University of Munich , Munich, Germany

12. Department of Neurosurgery, University Medical Center Hamburg-Eppendorf , Hamburg, Germany

13. Department of Quantitative Biomedicine, University of Zurich , Zurich, Switzerland

Abstract

Abstract Background The diffuse growth pattern of glioblastoma is one of the main challenges for accurate treatment. Computational tumor growth modeling has emerged as a promising tool to guide personalized therapy. Here, we performed clinical and biological validation of a novel growth model, aiming to close the gap between the experimental state and clinical implementation. Methods 124 patients from The Cancer Genome Archive (TCGA) and 397 patients from the UCSF Glioma Dataset were assessed for significant correlations between clinical data, genetic pathway activation maps (generated with PARADIGM; TCGA only), and infiltration (Dw) as well as proliferation (ρ) parameters stemming from a Fisher-Kolmogorov growth model. To further evaluate clinical potential, we performed the same growth modeling on preoperative MRI data from 30 patients of our institution and compared model-derived tumor volume and recurrence coverage with standard radiotherapy plans. Results The parameter ratio Dw/ρ(p < 0.05 in TCGA) as well as the simulated tumor volume (p < 0.05 in TCGA/ UCSF) were significantly inversely correlated with overall survival. Interestingly, we found a significant correlation between 11 proliferation pathways and the estimated proliferation parameter. Depending on the cutoff value for tumor cell density, we observed a significant improvement of recurrence coverage without significantly increased radiation volume utilizing model-derived target volumes instead of standard radiation plans. Conclusions Identifying a significant correlation between computed growth parameters, and clinical and biological data, we highlight the potential of tumor growth modeling for individualized therapy of glioblastoma. This might improve accuracy of radiation planning in the near future.

Publisher

Oxford University Press (OUP)

Subject

Surgery,Oncology,Neurology (clinical)

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