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Robust association between vascular habitats and patient prognosis in glioblastoma: An international multicenter study.
Del Mar Álvarez-Torres, María; Juan-Albarracín, Javier; Fuster-Garcia, Elies; Bellvís-Bataller, Fuensanta; Lorente, David; Reynés, Gaspar; Font de Mora, Jaime; Aparici-Robles, Fernando; Botella, Carlos; Muñoz-Langa, Jose; Faubel, Raquel; Asensio-Cuesta, Sabina; García-Ferrando, Germán A; Chelebian, Eduard; Auger, Cristina; Pineda, Jose; Rovira, Alex; Oleaga, Laura; Mollà-Olmos, Enrique; Revert, Antonio J; Tshibanda, Luaba; Crisi, Girolamo; Emblem, Kyrre E; Martin, Didier; Due-Tønnessen, Paulina; Meling, Torstein R; Filice, Silvano; Sáez, Carlos; García-Gómez, Juan M.
Afiliação
  • Del Mar Álvarez-Torres M; Universitat Politècnica de València, BDSLab, Instituto Universitarios de Tecnologías de la Información y Comunicaciones (ITACA), Valencia, Spain.
  • Juan-Albarracín J; Universitat Politècnica de València, BDSLab, Instituto Universitarios de Tecnologías de la Información y Comunicaciones (ITACA), Valencia, Spain.
  • Fuster-Garcia E; Oslo University Hospital, Department of Diagnostic Physics, Oslo, Norway.
  • Bellvís-Bataller F; Universitat Politècnica de València, BDSLab, Instituto Universitarios de Tecnologías de la Información y Comunicaciones (ITACA), Valencia, Spain.
  • Lorente D; Hospital Provincial de Castellón, Department of Medical Oncology, Castellón de la Plana, Castellón de la Plana, Spain.
  • Reynés G; Health Research Institute Hospital La Fe, Cancer Research Group, Valencia, Spain.
  • Font de Mora J; Instituto de Investigación Sanitaria La Fe, Laboratory of Cellular and Molecular Biology, Valencia, Spain.
  • Aparici-Robles F; Hospital Universitari i Politècnic La Fe, Área Clínica de imagen Médica, Valencia, Spain.
  • Botella C; Hospital Universitari i Politècnic La Fe, Área Clínica de Neurociencias, Valencia, Spain.
  • Muñoz-Langa J; Health Research Institute Hospital La Fe, Cancer Research Group, Valencia, Spain.
  • Faubel R; Universitat de València, Departament de Fisioteràpia, Valencia, Spain.
  • Asensio-Cuesta S; Universitat Politècnica de València, BDSLab, Instituto Universitarios de Tecnologías de la Información y Comunicaciones (ITACA), Valencia, Spain.
  • García-Ferrando GA; Universitat Politècnica de València, BDSLab, Instituto Universitarios de Tecnologías de la Información y Comunicaciones (ITACA), Valencia, Spain.
  • Chelebian E; Universitat Politècnica de València, BDSLab, Instituto Universitarios de Tecnologías de la Información y Comunicaciones (ITACA), Valencia, Spain.
  • Auger C; Hospital Vall d'Hebron, Universitat Autònoma de Barcelona, Magnetic Resonance Unit, Department of Radiology, Barcelona, Spain.
  • Pineda J; Hospital Clinic de Barcelona, Barcelona, Spain.
  • Rovira A; Hospital Vall d'Hebron, Universitat Autònoma de Barcelona, Magnetic Resonance Unit, Department of Radiology, Barcelona, Spain.
  • Oleaga L; Hospital Clinic de Barcelona, Barcelona, Spain.
  • Mollà-Olmos E; Hospital Universitario de la Ribera, Departamento de Radiodiagnóstico, Alzira, Valencia, Spain.
  • Revert AJ; Hospital de Manises, Manises, Valencia, Spain.
  • Tshibanda L; Centre Hospitalier Universitaire de Liège, Service médical de Radiodiagnostic, Liège, Belgium.
  • Crisi G; Azienda Ospedaliero-Universitaria di Parma, Neuroradiology, Parma, Italy.
  • Emblem KE; Oslo University Hospital, Department of Diagnostic Physics, Oslo, Norway.
  • Martin D; Centre Hospitalier Universitaire de Liege, Service de Neurochirurugie, Liège, Belgium.
  • Due-Tønnessen P; Oslo University Hospital Rikshospitalet, Department of Radiology, Oslo, Norway.
  • Meling TR; Oslo University Hospital, Department of Neurosurgery, Oslo, Norway.
  • Filice S; Geneva University Hospital, Department of Neurosurgery, Geneva, Switzerland.
  • Sáez C; Azienda Ospedaliero-Universitaria di Parma, Medical Physics, Parma, Italy.
  • García-Gómez JM; Universitat Politècnica de València, BDSLab, Instituto Universitarios de Tecnologías de la Información y Comunicaciones (ITACA), Valencia, Spain.
J Magn Reson Imaging ; 51(5): 1478-1486, 2020 05.
Article em En | MEDLINE | ID: mdl-31654541
ABSTRACT

BACKGROUND:

Glioblastoma (GBM) is the most aggressive primary brain tumor, characterized by a heterogeneous and abnormal vascularity. Subtypes of vascular habitats within the tumor and edema can be distinguished high angiogenic tumor (HAT), low angiogenic tumor (LAT), infiltrated peripheral edema (IPE), and vasogenic peripheral edema (VPE).

PURPOSE:

To validate the association between hemodynamic markers from vascular habitats and overall survival (OS) in glioblastoma patients, considering the intercenter variability of acquisition protocols. STUDY TYPE Multicenter retrospective study. POPULATION In all, 184 glioblastoma patients from seven European centers participating in the NCT03439332 clinical study. FIELD STRENGTH/SEQUENCE 1.5T (for 54 patients) or 3.0T (for 130 patients). Pregadolinium and postgadolinium-based contrast agent-enhanced T1 -weighted MRI, T2 - and FLAIR T2 -weighted, and dynamic susceptibility contrast (DSC) T2 * perfusion. ASSESSMENT We analyzed preoperative MRIs to establish the association between the maximum relative cerebral blood volume (rCBVmax ) at each habitat with OS. Moreover, the stratification capabilities of the markers to divide patients into "vascular" groups were tested. The variability in the markers between individual centers was also assessed. STATISTICAL TESTS Uniparametric Cox regression; Kaplan-Meier test; Mann-Whitney test.

RESULTS:

The rCBVmax derived from the HAT, LAT, and IPE habitats were significantly associated with patient OS (P < 0.05; hazard ratio [HR] 1.05, 1.11, 1.28, respectively). Moreover, these markers can stratify patients into "moderate-" and "high-vascular" groups (P < 0.05). The Mann-Whitney test did not find significant differences among most of the centers in markers (HAT P = 0.02-0.685; LAT P = 0.010-0.769; IPE P = 0.093-0.939; VPE P = 0.016-1.000). DATA

CONCLUSION:

The rCBVmax calculated in HAT, LAT, and IPE habitats have been validated as clinically relevant prognostic biomarkers for glioblastoma patients in the pretreatment stage. This study demonstrates the robustness of the hemodynamic tissue signature (HTS) habitats to assess the GBM vascular heterogeneity and their association with patient prognosis independently of intercenter variability. LEVEL OF EVIDENCE 3 Technical Efficacy Stage 2 J. Magn. Reson. Imaging 2020;511478-1486.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Glioblastoma Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Glioblastoma Tipo de estudo: Guideline / Observational_studies / Prognostic_studies / Risk_factors_studies Limite: Humans Idioma: En Ano de publicação: 2020 Tipo de documento: Article