Prognostic significance of growth kinetics in newly diagnosed glioblastomas revealed by combining serial imaging with a novel biomathematical model.

Glioblastomas are the most aggressive primary brain tumors, characterized by their rapid proliferation and diffuse infiltration of the brain tissue. Survival patterns in patients with glioblastoma have been associated with a number of clinicopathologic factors including age and neurologic status, yet a significant quantitative link to in vivo growth kinetics of each glioma has remained elusive. Exploiting a recently developed tool for quantifying glioma net proliferation and invasion rates in individual patients using routinely available magnetic resonance images (MRI), we propose to link these patient-specific kinetic rates of biological aggressiveness to prognostic significance. Using our biologically based mathematical model for glioma growth and invasion, examination of serial pretreatment MRIs of 32 glioblastoma patients allowed quantification of these rates for each patient's tumor. Survival analyses revealed that even when controlling for standard clinical parameters (e.g., age and Karnofsky performance status), these model-defined parameters quantifying biological aggressiveness (net proliferation and invasion rates) were significantly associated with prognosis. One hypothesis generated was that the ratio of the actual survival time after whatever therapies were used to the duration of survival predicted (by the model) without any therapy would provide a therapeutic response index (TRI) of the overall effectiveness of the therapies. The TRI may provide important information, not otherwise available, about the effectiveness of the treatments in individual patients. To our knowledge, this is the first report indicating that dynamic insight from routinely obtained pretreatment imaging may be quantitatively useful in characterizing the survival of individual patients with glioblastoma. Such a hybrid tool bridging mathematical modeling and clinical imaging may allow for stratifying patients for clinical studies relative to their pretreatment biological aggressiveness.

[1]  J Nucl Med , 2010 .

[2]  K. Swanson,et al.  A mathematical model for brain tumor response to radiation therapy , 2009, Journal of mathematical biology.

[3]  Kristin R. Swanson,et al.  Complementary but Distinct Roles for MRI and 18F-Fluoromisonidazole PET in the Assessment of Human Glioblastomas , 2008, Journal of Nuclear Medicine.

[4]  Thomas S Deisboeck,et al.  In silico cancer modeling: is it ready for prime time? , 2009, Nature Clinical Practice Oncology.

[5]  J M Wardlaw,et al.  Velocity of radial expansion of contrast-enhancing gliomas and the effectiveness of radiotherapy in individual patients: a proof of principle. , 2008, Clinical oncology (Royal College of Radiologists (Great Britain)).

[6]  Klaus Wienhard,et al.  Glioma Proliferation as Assessed by 3‘-Fluoro-3’-Deoxy-l-Thymidine Positron Emission Tomography in Patients with Newly Diagnosed High-Grade Glioma , 2008, Clinical Cancer Research.

[7]  Kristin R. Swanson,et al.  Quantifying glioma cell growth and invasion in vitro , 2008, Math. Comput. Model..

[8]  K. Swanson,et al.  A mathematical modelling tool for predicting survival of individual patients following resection of glioblastoma: a proof of principle , 2007, British Journal of Cancer.

[9]  Kristin R. Swanson,et al.  Modeling Diffusely Invading Brain Tumors An Individualized Approach to Quantifying Glioma Evolution and Response to Therapy , 2008 .

[10]  Nicola Bellomo,et al.  Selected topics in cancer modeling : genesis, evolution, immune competition, and therapy , 2008 .

[11]  G Powathil,et al.  Mathematical modeling of brain tumors: effects of radiotherapy and chemotherapy , 2007, Physics in medicine and biology.

[12]  K. Swanson,et al.  A mathematical model for glioma growth and invasion links biological aggressiveness assessed by MRI with hypoxia assessed by FMISO-PET , 2007 .

[13]  Kristin R Swanson,et al.  Using mathematical modeling to predict survival of low‐grade gliomas , 2007, Annals of neurology.

[14]  Kristin R. Swanson,et al.  The Evolution of Mathematical Modeling of Glioma Proliferation and Invasion , 2007, Journal of neuropathology and experimental neurology.

[15]  T. Deisboeck,et al.  Development of a three-dimensional multiscale agent-based tumor model: simulating gene-protein interaction profiles, cell phenotypes and multicellular patterns in brain cancer. , 2006, Journal of theoretical biology.

[16]  Webster K. Cavenee,et al.  WHO Classification of Tumours of the Central Nervous System. 4th Ed. , 2007 .

[17]  Michael Berens,et al.  A mathematical model of glioblastoma tumor spheroid invasion in a three-dimensional in vitro experiment. , 2007, Biophysical journal.

[18]  D. Louis WHO classification of tumours of the central nervous system , 2007 .

[19]  Alissa M. Weaver,et al.  Tumor Morphology and Phenotypic Evolution Driven by Selective Pressure from the Microenvironment , 2006, Cell.

[20]  Luc Taillandier,et al.  Prognostic value of initial magnetic resonance imaging growth rates for World Health Organization grade II gliomas , 2006, Annals of neurology.

[21]  J. Skołyszewski,et al.  Age and bromodeoxyuridine labelling index as prognostic factors in high-grade gliomas treated with surgery and radiotherapy. , 2006, Clinical oncology (Royal College of Radiologists (Great Britain)).

[22]  K. Aldape,et al.  Diagnostic, treatment, and demographic factors influencing survival in a population-based study of adult glioma patients in the San Francisco Bay Area. , 2006, Neuro-oncology.

[23]  Hervé Delingette,et al.  Realistic simulation of the 3-D growth of brain tumors in MR images coupling diffusion with biomechanical deformation , 2005, IEEE Transactions on Medical Imaging.

[24]  R. Guillevin,et al.  Simulation of anisotropic growth of low‐grade gliomas using diffusion tensor imaging , 2005, Magnetic resonance in medicine.

[25]  Marvin Bergsneider,et al.  Imaging proliferation in brain tumors with 18F-FLT PET: comparison with 18F-FDG. , 2005, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[26]  Martin J. van den Bent,et al.  Radiotherapy plus concomitant and adjuvant temozolomide for glioblastoma. , 2005, The New England journal of medicine.

[27]  James E. Morrow The University of Washington , 2004 .

[28]  J. Koudstaal,et al.  Analysis of Proliferation and Apoptosis in Brain Gliomas: Prognostic and Clinical Value , 2004, Journal of Neuro-Oncology.

[29]  Jan C Buckner,et al.  Factors influencing survival in high-grade gliomas. , 2003, Seminars in oncology.

[30]  Mark Muzi,et al.  Positron emission tomography imaging of brain tumors. , 2003, Neuroimaging clinics of North America.

[31]  E. Shaw,et al.  Reexamining the radiation therapy oncology group (RTOG) recursive partitioning analysis (RPA) for glioblastoma multiforme (GBM) patients , 2003 .

[32]  Kristin R. Swanson,et al.  Virtual resection of gliomas: Effect of extent of resection on recurrence , 2003 .

[33]  Laurent Capelle,et al.  Continuous growth of mean tumor diameter in a subset of grade II gliomas , 2003, Annals of neurology.

[34]  J. Murray,et al.  Quantifying Efficacy of Chemotherapy of Brain Tumors with Homogeneous and Heterogeneous Drug Delivery , 2002, Acta biotheoretica.

[35]  Z L Gokaslan,et al.  A multivariate analysis of 416 patients with glioblastoma multiforme: prognosis, extent of resection, and survival. , 2001, Journal of neurosurgery.

[36]  S. Torquato,et al.  Pattern of self‐organization in tumour systems: complex growth dynamics in a novel brain tumour spheroid model , 2001, Cell proliferation.

[37]  J. Murray,et al.  A quantitative model for differential motility of gliomas in grey and white matter , 2000, Cell proliferation.

[38]  M. Westphal,et al.  Glioma cell adhesion and migration on human brain sections. , 1998, Anticancer research.

[39]  D. Louis Collins,et al.  Design and construction of a realistic digital brain phantom , 1998, IEEE Transactions on Medical Imaging.

[40]  S. Brem,et al.  Survival rates in patients with primary malignant brain tumors stratified by patient age and tumor histological type: an analysis based on Surveillance, Epidemiology, and End Results (SEER) data, 1973-1991. , 1998, Journal of neurosurgery.

[41]  J. Murray,et al.  The interaction of growth rates and diffusion coefficients in a three-dimensional mathematical model of gliomas. , 1997, Journal of neuropathology and experimental neurology.

[42]  Alan C. Evans,et al.  BrainWeb: Online Interface to a 3D MRI Simulated Brain Database , 1997 .

[43]  J. Murray,et al.  A mathematical model of glioma growth: the effect of extent of surgical resection , 1996, Cell proliferation.

[44]  J. Murray,et al.  A mathematical model of glioma growth: the effect of chemotherapy on spatio‐temporal growth , 1995, Cell proliferation.

[45]  Charles B. Wilson,et al.  Cell kinetic analysis of human brain tumors by in situ double labelling with bromodeoxyuridine and iododeoxyuridine , 1992, International journal of cancer.

[46]  D. Lauffenburger,et al.  Receptor-mediated adhesion phenomena. Model studies with the Radical-Flow Detachment Assay. , 1990, Biophysical journal.

[47]  R. Barnard,et al.  The classification of tumours of the central nervous system. , 1982, Neuropathology and applied neurobiology.

[48]  Purves Mj,et al.  The physiology of the cerebral circulation. , 1972, Monographs of the Physiological Society.

[49]  J. D. de Oya [Physiology of the cerebral circulation]. , 1961, Revista clinica espanola.