Multicentre Validation of How Vascular Biomarkers From Tumor Can Predict the Survival of the Patient With Glioblastoma
NCT ID: NCT03439332
Last Updated: 2025-07-08
Study Results
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Basic Information
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COMPLETED
305 participants
OBSERVATIONAL
2018-02-07
2019-03-01
Brief Summary
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The Hemodynamic Multiparametric Tissue Signature (HTS) biomarker provides an automated unsupervised method to describe the heterogeneity of the enhancing tumor and edema areas in terms of the angiogenic process located at these regions. This allows to automatically draw 4 reproducible habitats that describe the tumor vascular heterogeneity:
* The High Angiogenic enhancing Tumor (HAT)
* The Less Angiogenic enhancing Tumor (LAT)
* The potentially tumor Infiltrated Peripheral Edema (IPE)
* The Vasogenic Peripheral Edema (VPE)
The conceptual hypothesis is that there is a significant correlation between the perfusion biomarkers located at several HTS habitats and the patient's overall survival.
The primary purpose of this clinical study is to determine if preoperative vascular heterogeneity of glioblastoma is predictive of overall survival of patients undergoing standard-of-care treatment by using the HTS biomarker.
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Detailed Description
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The main objective of the study is to determine if the habitats obtained by the Hemodynamic Multiparametric Tissue Signature (HTS) biomarker, which describe the tumor vascular heterogeneity of the enhancing tumor and edema areas, are predictive of the overall survival of patients undergoing standard-of-care treatment.
The specific objectives of the study are:
* To identify four habitats within the GBM using MRI and HTS
* To analyse the relation between the HTS habitats obtained from the first preoperative MRI and the overall survival of the patient
* To analyse the relation between HTS habitats obtained from the first preoperative MRI and the progression-free survival of the patient
* To analyse the relation between the HTS habitats obtained from the postradiotherapy MRI and the overall survival of the patient
* To analyse the relation between HTS habitats obtained from the postradiotherapy MRI and the progression-free survival of the patient
* To discover other interesting relations between the HTS habitats obtained from preoperative, postradiotherapy and follow-up images and the clinical conditions of the patients
Cox regression, Kaplan-Meier estimator and multiple linear regression analysis will be used to assess survival significance of each biomarker at each HTS habitat. The predictive value will be compared with models based on clinical and volumetric image variables: Age, Karnofsky Performance Status (KPS) Scale and Visually AcceSAble Rembrandt Images (VASARI) features. Moreover, the HTS-based models will be compared to models based on hemodynamic biomarkers, such as Cerebral Blood Flow (CBF), Cerebral Blood Volume (CBV), capillary permeability (Ktrans) and fractional Volume of Extravascular-Extracellular space (Ve), and diffusion biomarkers, such as Apparent Diffusion Coefficient (ADC), extracted from automatic segmentations of the edema and the enhancing tumor. Finally, Sørensen-Dice coefficient will be used to measure the correlation between MTS habitats in longitudinal studies.
Conditions
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Study Design
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CASE_ONLY
RETROSPECTIVE
Eligibility Criteria
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Inclusion Criteria
* Age \>18 years at diagnosis
* Patients with access to the preoperative and postradiotherapy MRI studies using 1.5 Tesla (T) or 3T scanners, including: pre and post gadolinium T1-weighted MRI, T2-weighted MRI, FLAIR MRI, Dynamic Susceptibility Contrast (DSC) T2\*-weighted perfusion, Dynamic Contrast Enhancement (DCE) T1-weighted perfusion (optional) and Diffusion Weighted Imaging (DWI) (optional)
* WHO performance score between 0 and 2
* Patients with Karnofsky Performance Score (KPS) of ≥ 70%
Exclusion Criteria
* Uncontrolled or significant cardiovascular disease, including: myocardial infarction and transient ischemic attack or stroke within 6 months prior to enrollment, uncontrolled angina within 6 months, diagnosed or suspected congenital long QT syndrome, any history of clinically significant ventricular arrhythmia (such as ventricular tachycardia, ventricular fibrillation or Torsades de pointes) and clinically significant abnormality on electrocardiogram (ECG)
* Pulmonary disease including or greater than grade 2 dyspnea or laryngeal edema, grade 3 pulmonary edema or pulmonary hypertension according to CTCAE 4.03
18 Years
ALL
No
Sponsors
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University of Liege
OTHER
Hospital de Manises
OTHER
Hospital de la Ribera
OTHER
Hospital Vall d'Hebron
OTHER
Hospital Clinic of Barcelona
OTHER
Azienda Ospedaliero-Universitaria di Parma
OTHER
Oslo University Hospital
OTHER
Juan M Garcia-Gomez
OTHER
Responsible Party
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Juan M Garcia-Gomez
Full professor
Principal Investigators
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Juan M Garcia Gomez, PhD
Role: PRINCIPAL_INVESTIGATOR
Universitat Politècnica de València
Locations
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Universitat Politècnica de València
Valencia, , Spain
Countries
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References
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Juan-Albarracin J, Fuster-Garcia E, Perez-Girbes A, Aparici-Robles F, Alberich-Bayarri A, Revert-Ventura A, Marti-Bonmati L, Garcia-Gomez JM. Glioblastoma: Vascular Habitats Detected at Preoperative Dynamic Susceptibility-weighted Contrast-enhanced Perfusion MR Imaging Predict Survival. Radiology. 2018 Jun;287(3):944-954. doi: 10.1148/radiol.2017170845. Epub 2018 Jan 19.
Juan-Albarracin J, Fuster-Garcia E, Manjon JV, Robles M, Aparici F, Marti-Bonmati L, Garcia-Gomez JM. Automated glioblastoma segmentation based on a multiparametric structured unsupervised classification. PLoS One. 2015 May 15;10(5):e0125143. doi: 10.1371/journal.pone.0125143. eCollection 2015.
Del Mar Alvarez-Torres M, Juan-Albarracin J, Fuster-Garcia E, Bellvis-Bataller F, Lorente D, Reynes G, Font de Mora J, Aparici-Robles F, Botella C, Munoz-Langa J, Faubel R, Asensio-Cuesta S, Garcia-Ferrando GA, Chelebian E, Auger C, Pineda J, Rovira A, Oleaga L, Molla-Olmos E, Revert AJ, Tshibanda L, Crisi G, Emblem KE, Martin D, Due-Tonnessen P, Meling TR, Filice S, Saez C, Garcia-Gomez JM. Robust association between vascular habitats and patient prognosis in glioblastoma: An international multicenter study. J Magn Reson Imaging. 2020 May;51(5):1478-1486. doi: 10.1002/jmri.26958. Epub 2019 Oct 26.
Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Related Links
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In order to allow the scientific community to test the biomarker, a non-commercial research purposes platform has been created. It offers the opportunity to upload cases of glioblastoma on which different services can be applied.
Other Identifiers
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UPV-2018-001
Identifier Type: -
Identifier Source: org_study_id
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