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ACRIN 6684: Assessment of Tumor Hypoxia in Newly Diagnosed Glioblastoma Using 18F-FMISO PET and MRI.
Gerstner, Elizabeth R; Zhang, Zheng; Fink, James R; Muzi, Mark; Hanna, Lucy; Greco, Erin; Prah, Melissa; Schmainda, Kathleen M; Mintz, Akiva; Kostakoglu, Lale; Eikman, Edward A; Ellingson, Benjamin M; Ratai, Eva-Maria; Sorensen, A Gregory; Barboriak, Daniel P; Mankoff, David A.
Afiliação
  • Gerstner ER; Massachusetts General Hospital Cancer Center, Boston, Massachusetts. Martinos Center for Biomedical Research, Charlestown, Massachusetts. egerstner@mgh.harvard.edu.
  • Zhang Z; Brown University, Providence, Rhode Island.
  • Fink JR; University of Washington, Seattle, Washington.
  • Muzi M; University of Washington, Seattle, Washington.
  • Hanna L; Brown University, Providence, Rhode Island.
  • Greco E; Brown University, Providence, Rhode Island.
  • Prah M; Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Schmainda KM; Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Mintz A; Wake Forest School of Medicine, Winston-Salem, North Carolina.
  • Kostakoglu L; Mount Sinai Medical Center, New York, NY.
  • Eikman EA; Moffitt Cancer Center, Tampa, Florida.
  • Ellingson BM; UCLA Medical Center, Los Angeles, California.
  • Ratai EM; Martinos Center for Biomedical Research, Charlestown, Massachusetts. Department of Radiology, Massachusetts General Hospital, Boston, Massachusetts.
  • Sorensen AG; Siemens Healthcare, Malvern, Pennsylvania.
  • Barboriak DP; Duke University Medical Center, Durham, North Carolina.
  • Mankoff DA; University of Pennsylvania, Philadelphia, Pennsylvania.
Clin Cancer Res ; 22(20): 5079-5086, 2016 Oct 15.
Article em En | MEDLINE | ID: mdl-27185374
ABSTRACT

PURPOSE:

Structural and functional alterations in tumor vasculature are thought to contribute to tumor hypoxia which is a primary driver of malignancy through its negative impact on the efficacy of radiation, immune surveillance, apoptosis, genomic stability, and accelerated angiogenesis. We performed a prospective, multicenter study to test the hypothesis that abnormal tumor vasculature and hypoxia, as measured with MRI and PET, will negatively impact survival in patients with newly diagnosed glioblastoma. EXPERIMENTAL

DESIGN:

Prior to the start of chemoradiation, patients with glioblastoma underwent MRI scans that included dynamic contrast enhanced and dynamic susceptibility contrast perfusion sequences to quantitate tumor cerebral blood volume/flow (CBV/CBF) and vascular permeability (ktrans) as well as 18F-Fluoromisonidazole (18F-FMISO) PET to quantitate tumor hypoxia. ROC analysis and Cox regression models were used to determine the association of imaging variables with progression-free and overall survival.

RESULTS:

Fifty patients were enrolled of which 42 had evaluable imaging data. Higher pretreatment 18F-FMISO SUVpeak (P = 0.048), mean ktrans (P = 0.024), and median ktrans (P = 0.045) were significantly associated with shorter overall survival. Higher pretreatment median ktrans (P = 0.021), normalized RCBV (P = 0.0096), and nCBF (P = 0.038) were significantly associated with shorter progression-free survival. SUVpeak [AUC = 0.75; 95% confidence interval (CI), 0.59-0.91], nRCBV (AUC = 0.72; 95% CI, 0.56-0.89), and nCBF (AUC = 0.72; 95% CI, 0.56-0.89) were predictive of survival at 1 year.

CONCLUSIONS:

Increased tumor perfusion, vascular volume, vascular permeability, and hypoxia are negative prognostic markers in newly diagnosed patients with gioblastoma, and these important physiologic markers can be measured safely and reliably using MRI and 18F-FMISO PET. Clin Cancer Res; 22(20); 5079-86. ©2016 AACR.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Imageamento por Ressonância Magnética / Glioblastoma / Tomografia por Emissão de Pósitrons / Hipóxia Tumoral / Neovascularização Patológica Idioma: En Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Neoplasias Encefálicas / Imageamento por Ressonância Magnética / Glioblastoma / Tomografia por Emissão de Pósitrons / Hipóxia Tumoral / Neovascularização Patológica Idioma: En Ano de publicação: 2016 Tipo de documento: Article